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        <title>Brain Tumor Pathology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Brain Tumor Pathology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Brain+Tumor+Pathology&t=Brain+Tumor+Pathology&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 20:43:00 +0100</lastBuildDate>
        <item>
            <title>A meningioma with peripheral rim enhancement on MRI</title>
            <link>http://www.medworm.com/index.php?rid=5660901&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq8r3nmj11x472318%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Meningiomas are common, typically benign intracranial neoplasms with well-demarcated borders. Meningiomas with indistinct
 boundaries have been reported. These can invade surrounding structures, and present surgical and diagnostic challenges. We
 present the case of an unusual meningioma in a 53-year-old male in which preoperative magnetic resonance imaging (MRI) revealed
 an irregular lesion with clear boundaries and peripheral rim enhancement. Intraoperatively, however, no cleavage plane was
 apparent. Histological examination showed an increase of fibroconnective tissue with proliferation of dilated vessels in the
 periphery of the tumor concordant with the rim. Immunohistochemical staining of the tumor was positive for EMA and CD34, but
 negative for CEA, Ki67, and ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660901</comments>
            <pubDate>Thu, 02 Feb 2012 18:12:00 +0100</pubDate>
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        <item>
            <title>Hematogenous extraneural metastasis of the germinomatous component of a pineal mixed germ cell tumor</title>
            <link>http://www.medworm.com/index.php?rid=5650063&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F77581674p645g233%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 23-year-old man presented with a mass in the pineal region and obstructive hydrocephalus. A neuroendoscopic biopsy for the
 lesion, ventriculoperitoneal (VP) shunting, and focal irradiation were conducted as initial treatment. Histological diagnosis
 of the biopsy specimen was germinoma. He underwent further irradiation and two tumor resections. Histological diagnosis was
 mature teratoma without a germinomatous component. After serial treatments, the intracranial lesion was controlled. However,
 14&amp;nbsp;months after presentation, extraneural lesions were confirmed in the posterior mediastinum and retroperitoneal space. The
 biopsy specimen of the retroperitoneal space lesion was histologically diagnosed as germinoma. Although chemotherapy with
 cisplatin and etoposid...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650063</comments>
            <pubDate>Fri, 27 Jan 2012 17:56:01 +0100</pubDate>
            <guid isPermaLink="false">5650063</guid>        </item>
        <item>
            <title>Anaplastic oligodendroglioma with ganglioglioma-like maturation</title>
            <link>http://www.medworm.com/index.php?rid=5584677&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu226j21310053546%2F</link>
            <description>We describe a case of anaplastic oligodendroglioma that was characterized by the presence of ganglion cells in a
 40-year-old-male. Histologically, the tumor was mainly composed of classical oligodendroglioma cells. The most exceptional
 finding of this tumor was the presence of ganglion cells and intermediate-sized ganglioid cells. Immunohistochemical analysis
 revealed that these cells were positive for Olig2 and negative for glial fibrillary acid protein (GFAP). Synaptophysin and
 microtubule-associated protein 2 (MAP2) were mainly detected in the ganglion cells. Fluorescence in situ hybridization analysis
 (FISH) revealed the deletion of the 1p and 19q chromosome arms in both the oligodendroglioma cells and ganglion cells. The
 R132H mutated isocitrate dehydrogenase 1 (IDH1) protein wa...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584677</comments>
            <pubDate>Tue, 10 Jan 2012 06:42:07 +0100</pubDate>
            <guid isPermaLink="false">5584677</guid>        </item>
        <item>
            <title>Ependymoma with cartilaginous metaplasia might have more aggressive behavior: a case report and literature review</title>
            <link>http://www.medworm.com/index.php?rid=5573065&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F91865v103r5162p9%2F</link>
            <description>We report a case of ependymoma with cartilaginous and osseous metaplasia in a 5-year-old boy. Microscopically,
 the tumor was composed of neoplastic ependymal tissue and mature cartilage and bone. Immunohistochemically, glial fibrillary
 acidic protein and epithelial membrane antigen were positive for ependymoma cells but negative for cartilage and bone. Recurrence
 occurred after 15-month follow-up. The patient deteriorated rapidly and died after 1&amp;nbsp;month. Reviewing 8 reported cases and
 our latest case, we found that 3 cases of ependymoma with cartilaginous metaplasia were treated with radiotherapy. Six cases
 had recurrence from 6&amp;nbsp;months to 8&amp;nbsp;years and 2 cases died on the day of operation. These findings suggest that ependymoma with
 cartilaginous metaplasia might have mor...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573065</comments>
            <pubDate>Fri, 06 Jan 2012 16:49:44 +0100</pubDate>
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        <item>
            <title>Glioblastoma angiogenesis: VEGF resistance solutions and new strategies based on molecular mechanisms of tumor vessel formation</title>
            <link>http://www.medworm.com/index.php?rid=5573066&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvx0309701n466p84%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioblastomas are highly vascular tumors. Recent preclinical and clinical investigations have revealed that agents targeting
 angiogenesis may have efficacy against this type of tumor. Antibodies to vascular endothelial growth factor are being studied
 in this patient population. Unfortunately, treatment inevitably fails. This review provides an update on recent research on
 the mechanisms by which tumor cells acquire resistance, and discusses recent preclinical and experimental development of novel
 new-generation anti-angiogenic agents that overcome this problem, especially those based on the molecular mechanisms of tumor
 vessel formation. The tumor vasculature not only nourishes glioblastomas, but also provides a specialized microenvironment
 for tumor stem-like cel...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573066</comments>
            <pubDate>Thu, 05 Jan 2012 06:52:53 +0100</pubDate>
            <guid isPermaLink="false">5573066</guid>        </item>
        <item>
            <title>Atypical teratoid rhabdoid tumor located in the pineal region following prophylactic irradiation for acute lymphoblastic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5573067&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc0755227708lj1kx%2F</link>
            <description>In this report, we present a case of a pineal region tumor causing
 acute hydrocephalus that could be pathologically diagnosed as AT/RT following prophylactic cranial irradiation for acute lymphoblastic
 leukemia.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-5DOI 10.1007/s10014-011-0075-8Authors
		Atsushi Kuge, Department of Neurosurgery, Yamagata University Faculty of Medicine, 2-2-2 Iidanishi, Yamagata, 990-9585 JapanShinya Sato, Department of Neurosurgery, Yamagata University Faculty of Medicine, 2-2-2 Iidanishi, Yamagata, 990-9585 JapanKaori Sakurada, Department of Neurosurgery, Yamagata University Faculty of Medicine, 2-2-2 Iidanishi, Yamagata, 990-9585 JapanSunao Takemura, Department of Neurosurgery, Yamagata University Faculty of Medicine, 2-2-2 Iidanishi, Yamagata, ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573067</comments>
            <pubDate>Thu, 05 Jan 2012 06:52:52 +0100</pubDate>
            <guid isPermaLink="false">5573067</guid>        </item>
        <item>
            <title>A rare case of primary bone xanthoma of the clivus</title>
            <link>http://www.medworm.com/index.php?rid=5573068&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq17jp730709600u6%2F</link>
            <description>This study introduces information regarding a bone xanthoma originating within the skull,
 together with a review of bone xanthoma literature.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-6DOI 10.1007/s10014-011-0073-xAuthors
		Kenichiro Asano, Department of Neurosurgery, Hirosaki University Graduate School of Medicine, Zaifu-cho 5, Hirosaki, Aomori 036-8562, JapanJyunko Sato, Department of Neurosurgery, Hirosaki University Graduate School of Medicine, Zaifu-cho 5, Hirosaki, Aomori 036-8562, JapanNaoya Matsuda, Department of Neurosurgery, Hirosaki University Graduate School of Medicine, Zaifu-cho 5, Hirosaki, Aomori 036-8562, JapanHiroki Ohkuma, Department of Neurosurgery, Hirosaki University Graduate School of Medicine, Zaifu-cho 5, Hirosaki, Aomori 036-8562, Japan
	

	
		...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573068</comments>
            <pubDate>Wed, 04 Jan 2012 06:58:34 +0100</pubDate>
            <guid isPermaLink="false">5573068</guid>        </item>
        <item>
            <title>Pleomorphic xanthoastrocytoma: a new differential diagnosis for a pediatric pineal neoplasm</title>
            <link>http://www.medworm.com/index.php?rid=5553298&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fuq8154434g476246%2F</link>
            <description>We describe its occurrence in an unusual location in a 15-year-old boy
 who presented with raised intracranial pressure of short duration. Imaging showed a 3&amp;nbsp;×&amp;nbsp;3.2&amp;nbsp;×&amp;nbsp;3.5&amp;nbsp;cm mass in the pineal region
 extending into the quadrigeminal cistern. It had a contrast-enhancing solid component and a larger, ventrally located, peripherally
 enhancing cystic component. Total excision of the lesion was achieved via a modified left Poppen’s approach. Histopathology
 and immunochemistry were suggestive of a PXA. This is the first report in the pediatric literature describing a PXA in the
 pineal region.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-4DOI 10.1007/s10014-011-0076-7Authors
		Sumit Thakar, Department of Neurosurgery, Sri Sathya Sai Institute of Hig...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5553298</comments>
            <pubDate>Tue, 27 Dec 2011 17:04:01 +0100</pubDate>
            <guid isPermaLink="false">5553298</guid>        </item>
        <item>
            <title>Pilocytic astrocytoma with abundant oligodendroglioma-like component</title>
            <link>http://www.medworm.com/index.php?rid=5553297&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F45p382473q578431%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;An 18-year-old girl presented with a history of visual disturbance without headache, nausea, or vomiting in May 2010. In July
 2010, the patient visited our hospital because of visual disturbance. Head magnetic resonance images revealed hydrocephalus
 caused by a ring-enhancing mass lesion located in the vermis. Total tumor removal was performed. Histological findings revealed
 that honeycomb cells resembling oligodendrocytes accounted for most parts of the tumor. Rosenthal fibers and hyaline droplets
 were seen in a small portion. The tumor cells were immunoreactive for GFAP and Olig2, but none of the tumor cells were immunoreactive
 for Symaptophysin, EMA, or IDH 1. according to these findings, the tumor was diagnosed as pilocytic astrocytoma with an abundant
 oligode...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5553297</comments>
            <pubDate>Tue, 27 Dec 2011 17:04:01 +0100</pubDate>
            <guid isPermaLink="false">5553297</guid>        </item>
        <item>
            <title>A huge intraventricular congenital anaplastic astrocytoma: case report with histopathological and genetic consideration</title>
            <link>http://www.medworm.com/index.php?rid=5478000&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F55n3646547v4r8x2%2F</link>
            <description>We present the clinical course
 and genetic alterations in an infant with a congenital malignant glioma detected incidentally by ultrasonography at 36&amp;nbsp;weeks.
 The tumor occupied the right temporoparietal region, extended to the posterior fossa, and significantly compressed surrounding
 structures. The female infant was entirely normal without macrocrania, tense fontanel, or sucking difficulties. The tumor
 was subtotally resected by two-stage surgery; pathological diagnosis was anaplastic astrocytoma. Immunohistochemical staining
 was positive for p53 and negative for epidermal growth factor receptor. There was no O6-methylguanine-DNA methyltransferase (MGMT) gene promoter methylation, no 1p/19q loss of heterozygosity, and no isocitrate dehydrogenase 1 (IDH1) mutation. She underwent p...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5478000</comments>
            <pubDate>Fri, 02 Dec 2011 18:08:00 +0100</pubDate>
            <guid isPermaLink="false">5478000</guid>        </item>
        <item>
            <title>Adult cerebellar glioblastoma cases have different characteristics from supratentorial glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=5410457&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5735k15n85l63372%2F</link>
            <description>This study is a histological and clinical investigation of four cases of cerebellar glioblastoma, a rare tumor. The cases
 included three males and one female, from 33 to 67&amp;nbsp;years in age (mean 49&amp;nbsp;years). Tumor resection, postoperative irradiation
 and chemotherapy were performed in all cases. Two patients died of local tumor recurrence after 14 and 27&amp;nbsp;months. Another
 patient relapsed after 10&amp;nbsp;months; however, after additional tumor resection and second line chemotherapy, she remains disease-free
 41&amp;nbsp;months after the initial treatment. The fourth patient has not relapsed in the 6&amp;nbsp;months since initial treatment. The histopathology
 of all cases was glioblastoma with pseudopalisading necrosis. However, low-grade glioma histopathology was found in three
 patients...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410457</comments>
            <pubDate>Thu, 10 Nov 2011 16:51:30 +0100</pubDate>
            <guid isPermaLink="false">5410457</guid>        </item>
        <item>
            <title>Rapid progression of rhabdoid components of a composite high-grade glioma and rhabdoid tumor in the occipital lobe of an adult</title>
            <link>http://www.medworm.com/index.php?rid=5389915&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3kx278u250153167%2F</link>
            <description>We report a very unusual case of a composite high-grade glioma and rhabdoid tumor in an adult. A 22-year-old woman presented
 with scintillating scotoma due to a solid tumor with surrounding brain edema in the right occipital lobe. The tumor was grossly
 resected. Histological examinations showed that the tumor was mainly composed of INI1-positive high-grade glioma tissue containing
 an INI1-negative rhabdoid component. She received radiation therapy and chemotherapy. Three months after the surgery, she
 again complained of visual disturbances, and tumor recurrence within the resection cavity was noted. A second operation was
 performed. The findings of histological examinations of the surgical specimen obtained during the second surgery were completely
 different from those of the specime...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5389915</comments>
            <pubDate>Tue, 01 Nov 2011 16:52:13 +0100</pubDate>
            <guid isPermaLink="false">5389915</guid>        </item>
        <item>
            <title>The expression of neuroglobin in astrocytoma</title>
            <link>http://www.medworm.com/index.php?rid=5338145&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1016231832510285%2F</link>
            <description>In this study, we aimed to explore the detailed expression of NGB in a rat astrocytoma cell line
 (C6) and human astrocytoma cell line (U251) by reverse transcription-polymerase chain reaction, immunofluorescence, and Western
 blotting, and to detect the expression of NGB in human astrocytoma tissues by an immunohistochemical method. We found that
 NGB was present in a rat astrocytoma cell line (C6), human astrocytoma cell line (U251), and human astrocytoma tissues. The
 expression and potential roles of NGB in astrocytomas may provide insight into the mechanisms of tumor cells to adapt and
 survive in hypoxic microenvironments and also represent a novel therapeutic approach to astrocytomas.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s10014-011-0066-9Aut...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338145</comments>
            <pubDate>Tue, 18 Oct 2011 15:56:27 +0100</pubDate>
            <guid isPermaLink="false">5338145</guid>        </item>
        <item>
            <title>Hemorrhagic onset of cerebellar pilocytic astrocytoma in an adult: a case report and review of the literature implying a possible relation of degenerative vascular changes to the massive intratumoral hemorrhage</title>
            <link>http://www.medworm.com/index.php?rid=5338146&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg16287v314p6085w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pilocytic astrocytoma (PA) is a low-grade astrocytic tumor arising predominantly during the first two decades of life. Hemorrhagic
 onset of PAs is uncommon, and the etiology of hemorrhage remains unclear. Here we report a case of hemorrhagic onset of cerebellar
 PA in a 29-year-old man who presented with a week-long history of headache and gait instability. Computed tomography and magnetic
 resonance imaging revealed a hemorrhagic tumor located in the right cerebellar hemisphere, and total resection was performed.
 Histological examination showed bipolar glial cell proliferation in a biphasic pattern in a compact area and a loose microcystic
 area with Rosenthal fibers and eosinophilic granular bodies, indicating PA. Prominent changes in tumor vasculature, including
 a...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338146</comments>
            <pubDate>Tue, 18 Oct 2011 15:56:26 +0100</pubDate>
            <guid isPermaLink="false">5338146</guid>        </item>
        <item>
            <title>Primary T-cell/histiocyte-rich B-cell lymphoma arising in the trigeminal ganglion in a patient with rheumatoid arthritis</title>
            <link>http://www.medworm.com/index.php?rid=5338147&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy1274l35423379rw%2F</link>
            <description>We report a cased of a 68-year-old man with primary T-cell/histiocyte-rich B-cell lymphoma (T/HRBCL) that arose in the trigeminal
 ganglion. He had a 30-year history of rheumatoid arthritis and presented with progressive left facial pain that had started
 3&amp;nbsp;weeks earlier. Magnetic resonance imaging (MRI) revealed an enhanced mass in the trigeminal ganglion and swelling of the
 distal part of the trigeminal root. The tumor, subtotally resected via the left anterior petrosal approach, was composed of
 proliferating CD30- and CD79-positive atypical large polygonal cells with hyperchromatic single or multiple nuclei. CD3-positive
 small lymphoid cells and CD68-positive histiocytic cells were intermingled with the neoplastic cells. These findings were
 compatible with T/HRBCL. After whole-...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338147</comments>
            <pubDate>Tue, 18 Oct 2011 15:56:25 +0100</pubDate>
            <guid isPermaLink="false">5338147</guid>        </item>
        <item>
            <title>A case of choroid plexus papilloma with stromal sclerosis and indistinct papillary structures</title>
            <link>http://www.medworm.com/index.php?rid=5298204&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx4502780v6633111%2F</link>
            <description>We present a case of choroid plexus papilloma with unusual histopathological findings. A 41-year-old Japanese man presented
 with dizziness. Brain magnetic resonance imaging scan showed a distinct mass in the fourth ventricle. Histopathological examination
 showed proliferation of cuboidal cells forming irregular trabeculae, small nests, and pseudoglandular and indistinct papillary
 structures, accompanied by a variable degree of stromal sclerosis. The tissue sections also showed rare mitotic activity,
 no hypercellularity, cellular pleomorphism, or necrosis. The immunohistochemical findings were tumor cells positive for cytokeratin
 7, vimentin, S-100 protein, and transthyretin but negative for cytokeratin 20, BerEP4 and carcinoembryonic antigen. These
 findings were consistent with choro...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5298204</comments>
            <pubDate>Tue, 04 Oct 2011 05:52:15 +0100</pubDate>
            <guid isPermaLink="false">5298204</guid>        </item>
        <item>
            <title>A case of metastatic brain tumor causing multifocal cerebral embolism</title>
            <link>http://www.medworm.com/index.php?rid=5252097&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdn4rm07507740v30%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The patient was a 72-year-old woman who had previously undergone treatment for femoral chondrosarcoma (histologically rated
 as myxofibrosarcoma). She suddenly developed left homonymous hemianopsia and was diagnosed with cerebral embolism. Because
 she had atrial fibrillation, we treated her for cardiogenic cerebral embolism. About 3&amp;nbsp;months later, however, she developed
 left hemiplegia, and head magnetic resonance imaging revealed multiple tumorous lesions affecting the previously detected
 infracted area and several new areas. We assumed that a tumor embolus had caused cerebral embolism, which resulted in growth
 of the tumor from the embolus and formation of a metastatic brain tumor. The metastatic foci formed from the tumor embolus
 were visualized by diagnosti...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5252097</comments>
            <pubDate>Wed, 21 Sep 2011 05:55:27 +0100</pubDate>
            <guid isPermaLink="false">5252097</guid>        </item>
        <item>
            <title>Lymphomatosis cerebri: clinical characteristics, neuroimaging, and pathological findings</title>
            <link>http://www.medworm.com/index.php?rid=5228100&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq26747v643712087%2F</link>
            <description>We present a case involving a 56-year-old
 immunocompetent woman who complained of rapid deterioration of her higher brain function over a 4-month period. Magnetic resonance
 imaging showed extensive white-matter lesions. During brain biopsy, a diffusely infiltrating lymphoma with distinctive immunohistochemical
 features was detected. Awareness of this unique presentation and early tissue diagnosis provide the best hope for instituting
 appropriate treatments.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-7DOI 10.1007/s10014-011-0064-yAuthors
		Ryuhei Kitai, Department of Neurosurgery, Faculty of Medical Sciences, University of Fukui, Fukui, JapanNorichika Hashimoto, Department of Neurosurgery, Faculty of Medical Sciences, University of Fukui, Fukui, JapanKouji Yamate, Depa...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5228100</comments>
            <pubDate>Fri, 16 Sep 2011 16:43:53 +0100</pubDate>
            <guid isPermaLink="false">5228100</guid>        </item>
        <item>
            <title>Neurohypophyseal germinoma with abundant fibrous tissue</title>
            <link>http://www.medworm.com/index.php?rid=5228101&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe25v620714155108%2F</link>
            <description>We report an unusual case of neurohypophyseal germinoma with abundant fibrous tissue and clival invasion that was initially
 misdiagnosed as lymphocytic hypophysitis. A 40-year-old woman presented with diabetes insipidus and panhypopituitarism after
 delivering her second son and which lasted for 4&amp;nbsp;years. Magnetic resonance imaging showed the intrasellar mass extending to
 the suprasellar region with enlarged pituitary stalk. The mass was heterogeneously enhanced and invaded the clivus. Biopsy
 of the intrasellar mass was performed via the trans-sphenoidal route, and histological examination revealed marked fibrous
 tissue and infiltration of lymphocytes, with no evidence of tumor cells. Lymphocytic hypophysitis was the initial diagnosis,
 and corticosteroid therapy was begun. Despite...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5228101</comments>
            <pubDate>Thu, 15 Sep 2011 05:45:22 +0100</pubDate>
            <guid isPermaLink="false">5228101</guid>        </item>
        <item>
            <title>The high mitotic count detected by phospho-histone H3 immunostain does not alter the benign behavior of angiocentric glioma</title>
            <link>http://www.medworm.com/index.php?rid=5198469&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc0826446u7504160%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Angiocentric glioma (AG) has been formally codified in the revised 2007 WHO Classification of Tumours of the Central Nervous
 System. AGs characteristically exhibit mixed features of ependymal and diffuse astrocytic differentiation and low proliferation
 rates, with Ki-67 labeling indices ranging from less than 1 to 5%. A single case with anaplastic recurrence and a labeling
 index of 10% has been reported. In the present study, we report a series of three AGs (Case 1: 4-year-old girl at right frontal
 lobe; Case 2: 4-year-old boy at left frontal lobe; Case 3: 9-year-old boy at right temporal lobe). Case 1 with elevated proliferation
 index (~10%) and increased mitotic activity (six mitoses per 10 high-power fields) on phospho-histone H3 (pHH3) immunostain
 at presentat...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5198469</comments>
            <pubDate>Sun, 04 Sep 2011 10:46:19 +0100</pubDate>
            <guid isPermaLink="false">5198469</guid>        </item>
        <item>
            <title>Microcystic meningioma presenting as a cystic lesion with an enhancing mural nodule in elderly women: report of three cases</title>
            <link>http://www.medworm.com/index.php?rid=5164397&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv1g0433363665551%2F</link>
            <description>We report a series of rare and unique presentation of microcystic meningioma in three elderly women aged 76
 (case 1), 72 (case 2), and 76 (case 3)&amp;nbsp;years, respectively. The first patient presented with a 3-year history of vertigo and
 past history of carotid artery stenosis, hypertension, and hypothyroidism. The second patient presented with headache and
 an acute episode of weakness in her legs. The third patient presented with headache, vomiting, and confusion. Magnetic resonance
 imaging for these three cases showed a cystic lesion with an enhancing mural nodule in the right frontal lobe. The preoperative
 differential diagnoses included hemangioblastoma and well-circumscribed gliomas for the first two cases. Glioblastoma and
 metastatic tumor were the working diagnoses for the thi...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5164397</comments>
            <pubDate>Tue, 23 Aug 2011 15:53:31 +0100</pubDate>
            <guid isPermaLink="false">5164397</guid>        </item>
        <item>
            <title>Hypoglossal nerve schwannoma with intratumoral hemorrhage</title>
            <link>http://www.medworm.com/index.php?rid=5127743&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft5721m35493x4657%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intratumoral hemorrhage of hypoglossal schwannoma is very rare. A 37-year-old man was admitted to our hospital with severe
 headache and gait disturbance. Radiologic examination revealed subarachnoid hemorrhage and a well-circumscribed enhanced lesion
 compressing the medulla oblongata. Gross total removal of the intracranial tumor was performed. Histopathological examination
 revealed the characteristic features of a schwannoma. The tumor had several hemorrhagic areas and numerous hyalinized blood
 vessels. Although the mechanism of hemorrhage from schwannomas is unclear, it is hypothesized that tumor vessels showing focal
 sinusoidal dilatation and hyaline thickening of the walls lead to spontaneous thrombosis with consequent necrosis, and often
 hemorrhage.
 
 
	Cont...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5127743</comments>
            <pubDate>Fri, 12 Aug 2011 06:17:08 +0100</pubDate>
            <guid isPermaLink="false">5127743</guid>        </item>
        <item>
            <title>Potential role of Jun activation domain-binding protein 1 and phosphorylated p27 expression in prognosis of glioma</title>
            <link>http://www.medworm.com/index.php?rid=5127742&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3204xpk302215405%2F</link>
            <description>In conclusion, the current results showed convincing evidence
 that the overexpression of Jab1, cytoplasmic p27, and pSer10p27 proteins is correlated with poor outcome in patients with
 glioma and that these three proteins may be useful markers to predict the prognosis of this tumor.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s10014-011-0061-1Authors
		Shi-ming He, Department of Neurosurgery, Institute for Functional Neurosurgery P.L.A, TangDu Hospital, Fourth Military Medical University, 710038 Xi’an, People’s Republic of ChinaZhen-wei Zhao, Department of Neurosurgery, Institute for Functional Neurosurgery P.L.A, TangDu Hospital, Fourth Military Medical University, 710038 Xi’an, People’s Republic of ChinaYuan Wang, Department of Neurosurgery, Institute for Functional Ne...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5127742</comments>
            <pubDate>Fri, 12 Aug 2011 06:17:08 +0100</pubDate>
            <guid isPermaLink="false">5127742</guid>        </item>
        <item>
            <title>Primary myxopapillary ependymoma of the fourth ventricle with cartilaginous metaplasia: a case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5127741&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu643466n24w4u80w%2F</link>
            <description>We report an additional case of intracranial MPE, which
 is the third reported case in the fourth ventricle. The tumor manifested in a 50-year-old lady, who presented with features
 of raised intracranial pressure. A gross total resection of the tumor was achieved. Histologically, the tumor had characteristic
 features of MPE with focal metaplastic cartilaginous deposit. On further evaluation, there was no evidence of a primary tumor
 in the spinal cord. Intracranial MPE needs further evaluation by craniospinal MRI to exclude an unrecognized primary in the
 spinal region, which could warrant surgical attention.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s10014-011-0059-8Authors
		Shrijeet Chakraborti, Department of Neuropathology, National Institute of Mental Health and Neurosci...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5127741</comments>
            <pubDate>Fri, 12 Aug 2011 06:17:08 +0100</pubDate>
            <guid isPermaLink="false">5127741</guid>        </item>
        <item>
            <title>Atypical and ischemic features of embolized meningiomas</title>
            <link>http://www.medworm.com/index.php?rid=5071920&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7973311q3x211230%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Preoperative embolization (POE) of meningiomas is widely used to facilitate surgical removal and to reduce intraoperative
 blood loss. The resulting necrosis and enhanced proliferation have been reported to affect subsequent histologic grading.
 However, there was little concern about ischemic features, for example small cells resembling atypical meningiomas, cytoplasmic
 vacuoles resembling clear cell meningioma, intercellular discohesion resembling rhabdoid meningioma, and perivascular cuffs
 resembling papillary meningioma. Therefore, the extent of these ischemic features was scored and Ki-67 staining indices were
 investigated in a POE group composed of 29 specimens of meningiomas treated with POE and compared with equivalent results
 for a non-POE group composed of...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5071920</comments>
            <pubDate>Mon, 25 Jul 2011 15:45:37 +0100</pubDate>
            <guid isPermaLink="false">5071920</guid>        </item>
        <item>
            <title>Metastatic brain sarcoma with gliomatous component</title>
            <link>http://www.medworm.com/index.php?rid=5058655&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft0811555k1374t18%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Here we report a metastatic brain carcinosarcoma from the uterus that posed a problem on diagnosis by containing an extensive
 gliomatous component. A 56-year woman developed motor aphasia 3&amp;nbsp;months after hysterectomy for a uterine tumor. Magnetic resonance
 imaging (MRI) demonstrated a left frontal cystic tumor, which was treated by stereotactic radiosurgery. The lesion recurred
 5&amp;nbsp;months later and was resected. Histological examination demonstrated neoplastic cells that were positive for glial fibrillary
 acidic protein (GFAP), leading to the diagnosis of high-grade glioma. This lesion recurred again after 9&amp;nbsp;months, and was resected
 again. The tumor tissue mostly consisted of GFAP-positive gliomatous cells, but close examination identified a sarcomatous...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5058655</comments>
            <pubDate>Thu, 21 Jul 2011 18:16:56 +0100</pubDate>
            <guid isPermaLink="false">5058655</guid>        </item>
        <item>
            <title>Grade II oligodendroglioma localized to the corpus callosum</title>
            <link>http://www.medworm.com/index.php?rid=5058656&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Faq82g28g5586186j%2F</link>
            <description>We present, to our knowledge, the first report of a grade II oligodendroglioma
 isolated within the corpus callosum with the characteristic molecular features of this tumor type. Histopathologic diagnosis
 is essential to appropriately guide therapy of callosal tumors.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s10014-011-0054-0Authors
		Edward A. Monaco, Department of Neurological Surgery, UPMC Presbyterian, University of Pittsburgh Medical Center, Suite B-400, 200 Lothrop Street, Pittsburgh, PA 15213, USAHenry B. Armah, Harper Hospital Pathology, Detroit Medical Center, Detroit, MI, USAMarina N. Nikiforova, Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA, USARonald L. Hamilton, Department of Pathology, University of Pittsburgh Medical Center, P...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5058656</comments>
            <pubDate>Thu, 21 Jul 2011 18:16:55 +0100</pubDate>
            <guid isPermaLink="false">5058656</guid>        </item>
        <item>
            <title>Diffuse large B-cell lymphoma within a cavernous hemangioma of the cavernous sinus</title>
            <link>http://www.medworm.com/index.php?rid=5058657&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frq236354166733v7%2F</link>
            <description>We report the case of a 72-year-old
 man with right circumorbital pain and right oculomotor nerve dysfunction because of a mass in the right cavernous sinus. It
 was removed via a transsphenoidal approach and histological examination revealed the mass was a cavernous hemangioma containing
 atypical large B cells in some sinusoidal vessels; no other evidence of lymphoma was detected on 18F-2-fluoro-2-deoxy-d-glucose positron-emission tomography or bone marrow biopsy. The patient underwent gamma knife radiosurgery (GKS) of the right
 cavernous sinus, but no systemic chemotherapy was administered. Although good local control was achieved, the patient developed
 a systemic diffuse large B-cell lymphoma (DLBCL) 1.5&amp;nbsp;years after the GKS. The atypical lymphocytes of the cavernous hemangioma
 ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5058657</comments>
            <pubDate>Thu, 21 Jul 2011 18:16:54 +0100</pubDate>
            <guid isPermaLink="false">5058657</guid>        </item>
        <item>
            <title>Spindle cell oncocytoma of the adenohypophysis</title>
            <link>http://www.medworm.com/index.php?rid=5058659&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg393411u87875832%2F</link>
            <description>We describe an SCO in an adult, a 42-year-old woman whose magnetic resonance (MR) images documented
 an intrasellar lesion located in the hypophysis. Histopathological examination showed a tumor composed predominantly of spindle
 cells. Immunohistochemical studies showed positivity for vimentin, S10, EMA, and antimitochondrial antibody MU213-UC clone
 131. Cytokeratin (CK) (AE1/AE3), glial fibrillary acidic protein (GFAP), chromogranin, synaptophysin, PGP9.5, CD57, desmin,
 D2-40, smooth muscle actin (SMA), Bcl-2, progesterone receptor, and CD34 were negative. Neuropeptides were negative. With
 electron microscopy, the neoplastic cells appear filled with mitochondria, well-formed desmosomes, but lacked secretory granules.
 SPO is a rare non-endocrine neoplasm of the adenohypophysis with be...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5058659</comments>
            <pubDate>Thu, 21 Jul 2011 18:16:53 +0100</pubDate>
            <guid isPermaLink="false">5058659</guid>        </item>
        <item>
            <title>Anaplastic ependymoma simulating glioblastoma in the cerebrum of an adult</title>
            <link>http://www.medworm.com/index.php?rid=5058658&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq72l31021754j6g1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A case of anaplastic ependymoma of the cerebral hemisphere in which the histopathological features closely simulated those
 of glioblastoma is reported. The patient was a 72-year-old woman with a large, well-demarcated tumor in the left temporal
 lobe. The tumor was totally extirpated, but recurred 18&amp;nbsp;months later, and the patient died after 4&amp;nbsp;months. The extirpated
 tumor was well circumscribed from the surrounding brain tissue and consisted of a sheet-like, dense proliferation of atypical,
 short spindle or polygonal cells. Extensive geographic necrosis with nuclear pseudopalisading was seen. Although perivascular
 pseudorosettes were observed in many areas, true ependymal rosettes were absent. Immunohistochemistry for glial fibrillary
 acidic protein and ep...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5058658</comments>
            <pubDate>Thu, 21 Jul 2011 18:16:53 +0100</pubDate>
            <guid isPermaLink="false">5058658</guid>        </item>
        <item>
            <title>Erratum to: Loss of heterozygosity analysis in malignant gliomas</title>
            <link>http://www.medworm.com/index.php?rid=5031884&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb7110tw6w1pr0281%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s10014-011-0049-xAuthors
		Masahiro Mizoguchi, Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582 JapanDaisuke Kuga, Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582 JapanYanlei Guan, Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582 JapanNobuhiro Hata, Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582 JapanAkira Nakamizo, Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higa...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5031884</comments>
            <pubDate>Wed, 13 Jul 2011 06:16:42 +0100</pubDate>
            <guid isPermaLink="false">5031884</guid>        </item>
        <item>
            <title>New insights into glioma classification based on isocitrate dehydrogenase 1 and 2 gene status</title>
            <link>http://www.medworm.com/index.php?rid=5012712&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff7t135472p861g45%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In glioma, mutations in the isocitrate dehydrogenase 1 and 2 (IDH1/2) genes have been receiving attention. IDH1/2 mutations are frequently found in grade II and III gliomas. These genetic alterations occur very early in gliomagenesis and
 strongly predict favorable outcome in patients with high-grade gliomas. Despite the evolution of studies on this topic, the
 underlying mechanism of the IDH1/2 mutations remains unknown. Here, we briefly review the current knowledge of IDH1/2 and discuss molecular diagnostics based on IDH1/2 gene status.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s10014-011-0050-4Authors
		Ichiyo Shibahara, Department of Neurosurgery, Tohoku University School of Medicine, 1-1 Seiryo-machi Aoba-ku, Sendai, 980-8575 JapanYukihiko Sonoda, Depar...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5012712</comments>
            <pubDate>Thu, 07 Jul 2011 05:45:01 +0100</pubDate>
            <guid isPermaLink="false">5012712</guid>        </item>
        <item>
            <title>A case of lymphoplasmacyte-rich meningioma of the jugular foramen</title>
            <link>http://www.medworm.com/index.php?rid=4994571&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv7314hj35m27h376%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Lymphoplasmacyte-rich meningioma (LPRM), the most rare variant of meningiomas, features extensive lymphoplasmacytic infiltrates.
 Although the jugular foramen (JF) is occasionally involved by several types of tumor, such as paragangliomas and schwannomas,
 meningioma in the JF is an infrequent disease. Here we present an extremely rare case of LPRM found in the JF. A 55-year-old
 woman complained of paresis in her right eyelid and palsy in the right side of her lip. Hoarseness and dysphagia also occurred
 in the following month. Radiologic examinations disclosed a mass lesion in the right JF, and the tumor was operatively removed.
 Microscopically, the tumor was composed of extensive lymphoplasmacytic infiltration with mild vascular proliferation and scattered
 sheets o...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4994571</comments>
            <pubDate>Fri, 01 Jul 2011 17:42:23 +0100</pubDate>
            <guid isPermaLink="false">4994571</guid>        </item>
        <item>
            <title>Oligodendroglial ganglioglioma</title>
            <link>http://www.medworm.com/index.php?rid=4994572&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F481ju00741408725%2F</link>
            <description>We present a case
 of a 40-year-old woman with ganglioglioma consisting mostly of oligodendroglial components. Magnetic resonance imaging showed
 a well-demarcated cystic lesion with slight perifocal edema in the right parietal lobe. The wall of the cyst was not enhanced
 after administration of Gd-DTPA contrast media. The mass was totally resected. Histological examination showed a mixture of
 two distinct components: oligodendroglioma and dysplastic ganglions. The first component was diffusely proliferated cells
 with round nuclei and perinuclear halo; the second showed marked nucleoli and basophilic cytoplasm containing Nissl bodies.
 Immunohistochemical study of the oligodendroglial component was positive for OLIG 2 and NKX2.2 but negative for synaptophysin.
 In addition, LOH of 1p/19q...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4994572</comments>
            <pubDate>Fri, 01 Jul 2011 17:42:22 +0100</pubDate>
            <guid isPermaLink="false">4994572</guid>        </item>
        <item>
            <title>Expression of stem cell marker and receptor kinase genes in glioblastoma tissue quantified by real-time RT-PCR</title>
            <link>http://www.medworm.com/index.php?rid=4963477&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk3140254584l7925%2F</link>
            <description>In this study, we quantified RNA expression levels of stem cell markers [CD133, Nestin, BMI-1, maternal embryonic leucine
 zipper kinase (MELK), and Notch1–4] as well as RTKs (EGFR, ErbB4, VEGFR1-3, FGFR1, -2, PDGFRΑ, and PDGFRΒ) in 42 clinical
 samples of glioblastoma by the real-time RT-PCR method. We demonstrated that the expression of MELK is exclusively upregulated
 in glioblastoma tissue. Notch receptor expression is moderately upregulated and is correlated with that of VEGFR2, VEGFR3,
 and PDGFRβ. Unsupervised clustering identified one unique sample group that showed high expression of most of the genes analyzed.
 Our results suggest that quantification of these stem cell markers and RTK genes can stratify patients based on the expression
 profile, which might provide insight i...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4963477</comments>
            <pubDate>Tue, 21 Jun 2011 16:42:22 +0100</pubDate>
            <guid isPermaLink="false">4963477</guid>        </item>
        <item>
            <title>Meningioangiomatosis-associated meningioma misdiagnosed as glioma by radiologic and intraoperative histological examinations</title>
            <link>http://www.medworm.com/index.php?rid=4947403&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8g42761g04781675%2F</link>
            <description>We report here a case of meningioangiomatosis-associated
 meningioma misdiagnosed as glioma by preoperative radiologic and intraoperative histological examinations. A 50-year-old woman
 presented with a 1-year history of headache and dizziness. Magnetic resonance imaging revealed a round left temporal mass
 located cortically with hypointensity on T1-weighted images and hyperintensity on T2-weighted images. In the intraoperative histological examination, a diagnosis of glioma was made based on high cellularity
 and large tumor cells with nuclear atypia. However, postoperative histological diagnosis of the lesion was meningioangiomatosis-associated
 meningioma corresponding to World Health Organization (WHO) grade I. A part of the cortical lesion showed the histological
 features of meningi...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4947403</comments>
            <pubDate>Fri, 17 Jun 2011 11:57:10 +0100</pubDate>
            <guid isPermaLink="false">4947403</guid>        </item>
        <item>
            <title>Preface</title>
            <link>http://www.medworm.com/index.php?rid=4947404&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyq687r92kk862612%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s10014-011-0044-2Authors
		Toshihiko Kuroiwa, Department of Neurosurgery, Osaka Medical College, Takatsuki, Japan
	

	
		Journal Brain Tumor PathologyOnline ISSN 1861-387XPrint ISSN 1433-7398 (Source: Brain Tumor Pathology)</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4947404</comments>
            <pubDate>Fri, 17 Jun 2011 11:57:08 +0100</pubDate>
            <guid isPermaLink="false">4947404</guid>        </item>
        <item>
            <title>A case of anaplastic clear-cell ependymoma presenting with high erythropoietin concentration and 1p/19q deletions</title>
            <link>http://www.medworm.com/index.php?rid=4915492&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F01335w66253787v8%2F</link>
            <description>We describe a 19-year-old woman with onset of epileptic seizure, and a small mural nodule and multicystic lesions with severe
 brain edema located in the right frontal lobe. At surgery, the tumor and a clear margin was removed, and symptoms improved
 postoperatively. Extended local radiotherapy (60&amp;nbsp;Gy) was performed. Histopathological examination revealed oligodendroglioma-like
 tumor cells with a perinuclear halo. The tumor cells extended processes toward CD34-positive proliferating vessels, which
 resemble a basement membrane. These proliferating vessels formed a tumor membrane so that there was a clear margin between
 the tumor and brain tissue. Tumor cells were positive for epithelial membrane antigen in a dot-like pattern. MIB-1 staining
 index was 50.6%. Electron microscopy show...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4915492</comments>
            <pubDate>Sat, 04 Jun 2011 05:52:49 +0100</pubDate>
            <guid isPermaLink="false">4915492</guid>        </item>
        <item>
            <title>Cerebellopontine angle endodermal cyst presenting with hemifacial spasm</title>
            <link>http://www.medworm.com/index.php?rid=4915494&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff357q544021531l1%2F</link>
            <description>We report a right cerebellopontine
 angle (CPA) endodermal cyst in a 56-year-old man who presented with a 6-month history of right-sided hemifacial spasm. Computed
 tomography revealed a homogenous, well-demarcated, hyperdense lesion extending from prepontine cistern to right CPA. Magnetic
 resonance imaging demonstrated a right CPA extra-axial cystic lesion protruding into Meckel’s cave, with compression of cranial
 nerves VII and VIII. Light brown, creamy cystic content was totally removed, and the thin cyst wall surrounding cranial nerves
 VII and VIII and the right vertebral artery was subtotally removed through the right lateral suboccipital approach. On microscopic
 examination, the cyst wall was composed of mono- to multilayered stratified epithelia, which were lined by ciliated o...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4915494</comments>
            <pubDate>Sat, 04 Jun 2011 05:52:48 +0100</pubDate>
            <guid isPermaLink="false">4915494</guid>        </item>
        <item>
            <title>Histopathologic and immunohistochemical profile of spinal glioblastoma: a study of six cases</title>
            <link>http://www.medworm.com/index.php?rid=4915493&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpp2817404u760r00%2F</link>
            <description>We describe the detailed histopathological and immunohistochemical
 profiles of six cases of spinal glioblastoma. Most of the tumors were located in the cervical or cervicothoracic region. The
 majority of the patients were young adults (mean age 34.8&amp;nbsp;years), presenting with a short duration of symptoms of 2&amp;nbsp;months
 or less. Their histopathological features were similar to cerebral glioblastoma. Diverse vascular changes like microvascular
 proliferation, sprouting angiogenesis, sclerosed and thrombosed vessels, along with field necrosis were prominent findings.
 All tumors were positive for GFAP and negative for EMA. The MIB-1 labeling index was very high (mean 16.7 ± 3.2%). Five out
 of six tumors were immunoreactive for p53 protein, and only two showed over-expression of EGFR ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4915493</comments>
            <pubDate>Sat, 04 Jun 2011 05:52:48 +0100</pubDate>
            <guid isPermaLink="false">4915493</guid>        </item>
        <item>
            <title>Loss of heterozygosity analysis in malignant gliomas</title>
            <link>http://www.medworm.com/index.php?rid=4896798&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg813570h56646lk1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Despite recent advances in the diagnosis and treatment of glioblastomas, patient outcomes for these highly malignant tumors
 remain poor. Research into the molecular pathology of glioblastoma has uncovered various genetic changes that contribute to
 malignancy. Some of the identified molecular markers—such as loss of heterozygosity (LOH) on chromosome 1p/19q and chromosome
 10, O6-methylguanine methyltransferase promoter hypermethylation, and mutation of isocitrate dehydrogenase-1—may help to predict
 patient outcomes. Indeed, LOH analysis is an effective approach to classify malignant gliomas. Genome-wide analyses have revealed
 that the extent and pattern of LOH regions may have important implications for the clinical course of the disease. As the
 genetic underpi...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4896798</comments>
            <pubDate>Wed, 01 Jun 2011 05:50:30 +0100</pubDate>
            <guid isPermaLink="false">4896798</guid>        </item>
        <item>
            <title>Molecular and clinical analysis of glioblastoma with an oligodendroglial component (GBMO)</title>
            <link>http://www.medworm.com/index.php?rid=4896799&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp651037185138821%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The genetic and clinical features of glioblastoma with an oligodendroglial component (GBMO), pathologically defined as anaplastic
 oligo-astrocytoma with necrosis, remain unclear. We investigated the correlation between genetic alterations and clinical
 outcomes in 19 GBMO patients we have encountered since 1997. Using single nucleotide polymorphism oligonucleotide genomic
 (SNP) microarrays, we analyzed gene amplification, loss of heterozygosity (LOH), and homozygous deletions in their whole genome.
 We also analyzed their overall survival (OS). Pathological studies revealed the presence of calcification in 11 and of a cyst
 in 9 of the 19 patients. Whole-genome analysis using SNP microarrays revealed LOH of chromosome 10 in 11, EGFR amplification
 in 8, 9p21 (INK4 loc...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4896799</comments>
            <pubDate>Wed, 01 Jun 2011 05:50:29 +0100</pubDate>
            <guid isPermaLink="false">4896799</guid>        </item>
        <item>
            <title>Papillary tumor of the pineal region</title>
            <link>http://www.medworm.com/index.php?rid=4896800&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe2776l514462411w%2F</link>
            <description>We report a case
 of PTPR, and undertake a literature review of this rare neuroepithelial neoplasm. Patients with PTPR need long-term follow
 up, and new cases should be well documented so that we can gain a better understanding of this neoplasm.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s10014-011-0040-6Authors
		Gerival Vieira Júnior, Neurosurgery Division of the Santa Casa de Belo Horizonte, Belo Horizonte, MG, BrazilMarcos Dellaretti, Neurosurgery Division of the Santa Casa de Belo Horizonte, Belo Horizonte, MG, BrazilGervásio Teles Cardoso de Carvalho, Neurosurgery Division of the Santa Casa de Belo Horizonte, Belo Horizonte, MG, BrazilRafael Augusto Castro Santiago Brandão, Neurosurgery Division of the Santa Casa de Belo Horizonte, Belo Horizonte, MG, BrazilArnoldo Maf...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4896800</comments>
            <pubDate>Wed, 01 Jun 2011 05:50:27 +0100</pubDate>
            <guid isPermaLink="false">4896800</guid>        </item>
        <item>
            <title>A miR-21 inhibitor enhances apoptosis and reduces G2-M accumulation induced by ionizing radiation in human glioblastoma U251 cells</title>
            <link>http://www.medworm.com/index.php?rid=4896801&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8024051215531021%2F</link>
            <description>In this study, we found that miR-21 expression was upregulated in response to ionizing radiation (IR) in U251 cells, which
 suggested that miR-21 could be involved in the response of U251 cells to radiation. We showed that a miR-21 inhibitor enhanced
 IR-induced glioblastoma cell growth arrest and increased the level of apoptosis, which was probably caused by abrogation of
 the G2-M arrest induced by IR. Further research demonstrated that the miR-21 inhibitor induced the upregulation of Cdc25A. Taken
 together, these findings suggest that miR-21 inhibitor can increase IR-induced growth arrest and apoptosis in U251 glioblastoma
 cells, at least in part by abrogating G2-M arrest, and that Cdc25A is a potential target of miR-21.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s10014-011...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4896801</comments>
            <pubDate>Thu, 26 May 2011 16:12:05 +0100</pubDate>
            <guid isPermaLink="false">4896801</guid>        </item>
        <item>
            <title>Unclassified glioneuronal tumor with advanced lipidization</title>
            <link>http://www.medworm.com/index.php?rid=4823271&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu6687234t8354988%2F</link>
            <description>We report a unique case of mixed glioneuronal
 tumor with marked lipomatous changes in a young patient with intractable epilepsy. MRI revealed a well-circumscribed lesion
 in the right temporal lobe. Histopathological findings showed the pleomorphic tumor with numerous cells containing large lipid
 droplets, resembling mature adipocytes, that were arranged in clusters or scattered within the neoplastic tissue. The tumor
 was composed of both glial and neuronal elements. Some tumor cells displayed features intermediate between glial and neuronal
 cells. The reticulin fibers were limited to blood vessels. Mitotic figures, vascular proliferation, and necrosis were absent,
 and MIB-1 labeling index was less than 1%. Diffuse immunoreactivity for GFAP and S100-protein was observed. In some heavi...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4823271</comments>
            <pubDate>Wed, 11 May 2011 15:47:09 +0100</pubDate>
            <guid isPermaLink="false">4823271</guid>        </item>
        <item>
            <title>Extraaxial neurocytoma in the skull base</title>
            <link>http://www.medworm.com/index.php?rid=4823272&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj3g6h504qr295881%2F</link>
            <description>We report a rare case of an extraaxial neurocytoma in the sphenocavernous-petroclival region
 that was successfully treated by radiation therapy following partial removal and pathological evaluation of the tumor.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s10014-011-0035-3Authors
		Satoka Shidoh, Department of Neurosurgery, Keio University Hospital, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582 JapanKazunari Yoshida, Department of Neurosurgery, Keio University Hospital, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582 JapanKatsuya Saitoh, Department of Neurosurgery, Keio University Hospital, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582 JapanTokuhiro Kimura, Division of Diagnostic Pathology, Keio University Hospital, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582 JapanYuichiro Hayas...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4823272</comments>
            <pubDate>Wed, 11 May 2011 15:47:07 +0100</pubDate>
            <guid isPermaLink="false">4823272</guid>        </item>
        <item>
            <title>Langerhans cell histiocytosis in endoscopic biopsy: marked pinching artifacts by endoscopy</title>
            <link>http://www.medworm.com/index.php?rid=4784104&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyp5782212534121k%2F</link>
            <description>We report the eighth case that provides neurologists, radiologists, and pathologists
 with various implications.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s10014-011-0034-4Authors
		Songmi Noh, Department of Pathology, Yonsei University, College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul, 120-752 KoreaDong-Seok Kim, Department of Pediatric Neurosurgery, Yonsei University, College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul, 120-752 KoreaJinna Kim, Department of Radiology, Yonsei University, College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul, 120-752 KoreaSe Hoon Kim, Department of Pathology, Yonsei University, College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul, 120-752 Korea
	

	
		Journal Brain Tumor PathologyOnline ISSN 1861-387XPrint ISSN 1433-7398 (So...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4784104</comments>
            <pubDate>Wed, 27 Apr 2011 16:26:31 +0100</pubDate>
            <guid isPermaLink="false">4784104</guid>        </item>
        <item>
            <title>A case of multinodular high-grade neuroepithelial tumor with ependymal differentiation</title>
            <link>http://www.medworm.com/index.php?rid=4694338&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F881nx8u30278101r%2F</link>
            <description>We describe a rare case of multinodular cerebral neuroepithelial tumor with ependymal differentiation. A 65-year-old man experienced
 loss of consciousness with an obscure episode of seizure attack. Magnetic resonance images disclosed a lesion located in the
 left temporal lobe and the insular cortex. The tumor was partially removed. Histologically, the tumor showed infiltrating
 multinodular tumor nodules in the cerebrum. Each nodule was well demarcated and composed of clear cells with perinuclear halos,
 intermingled fibrillary cells, and poorly differentiated neuroepithelial cells with mitotic activity. Immunohistochemically,
 clear cells showed dot-like positivity for epithelial membrane antigen. Fibrillary cells were positive for vimentin and nestin,
 whereas only a few glial fibrilla...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4694338</comments>
            <pubDate>Thu, 07 Apr 2011 17:11:00 +0100</pubDate>
            <guid isPermaLink="false">4694338</guid>        </item>
        <item>
            <title>Erratum to: Detection of IDH1 mutation in human gliomas: comparison of immunohistochemistry and sequencing</title>
            <link>http://www.medworm.com/index.php?rid=4672514&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcmp4082mt477r38l%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s10014-011-0028-2Authors
		Shingo Takano, Department of Neurosurgery, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8575, JapanWei Tian, Molecular Tumor Marker Research Team, The Oncology Research Center, Advanced Molecular Epidemiology Research Institute, Yamagata University Faculty of Medicine, 2-2-2 Iida-nishi, Yamagata, 990-9585 JapanMasahide Matsuda, Department of Neurosurgery, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8575, JapanTetsuya Yamamoto, Department of Neurosurgery, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8575, JapanEiichi Ishikawa, Department of Neurosurgery, Institute of Clin...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4672514</comments>
            <pubDate>Thu, 31 Mar 2011 17:38:50 +0100</pubDate>
            <guid isPermaLink="false">4672514</guid>        </item>
        <item>
            <title>Genetic profile of astrocytic and oligodendroglial gliomas</title>
            <link>http://www.medworm.com/index.php?rid=4646188&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F617j32101xlr2n17%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Low-grade diffuse gliomas WHO grade II (diffuse astrocytoma, oligoastrocytoma, oligodendroglioma) are characterized by frequent
 IDH1/2 mutations (&amp;gt;80%) that occur at a very early stage. In addition, the majority of diffuse astrocytomas (about 60%) carry TP53 mutations, which constitute a prognostic marker for shorter survival. Oligodendrogliomas show frequent loss at 1p/19q (about
 70% of cases), which is associated with longer survival. With respect to clinical outcome, molecular classification on the
 basis of IDH1/2 mutations, TP53 mutations, and 1p/19q loss showed a predictive power similar to histological classification. IDH1/2 mutations are frequent (&amp;gt;80%) in secondary glioblastomas that have progressed from low-grade or anaplastic astrocytomas.
 Primary (d...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4646188</comments>
            <pubDate>Fri, 25 Mar 2011 18:50:34 +0100</pubDate>
            <guid isPermaLink="false">4646188</guid>        </item>
        <item>
            <title>Metabolic assessment of monofocal acute inflammatory demyelination using MR spectroscopy and 11C-methionine-, 11C-choline-, and 18F-fluorodeoxyglucose-PET</title>
            <link>http://www.medworm.com/index.php?rid=4646191&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flw4730m543176684%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Monofocal acute inflammatory demyelination (MAID), which is observable by CT and MRI as a well-enhanced mass lesion with prominent
 perifocal edema, is very similar to malignant gliomas radiologically, making differential diagnosis of the two pathologies
 difficult. The aim of this study was to assess the different metabolic activities between MAID and malignant gliomas by MRS,
 methionine-PET, choline-PET, and FDG-PET. Six patients with MAID underwent methionine, choline, and FDG-PET, and 4 of the
 patients also underwent magnetic resonance spectroscopy (MRS). The images obtained from these patients were compared with
 the corresponding images of 19 anaplastic astrocytomas (AA) and 21 glioblastomas (GBM). The mean choline/creatine ratio of
 MAID was significantly lower...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4646191</comments>
            <pubDate>Fri, 25 Mar 2011 18:50:32 +0100</pubDate>
            <guid isPermaLink="false">4646191</guid>        </item>
        <item>
            <title>MGMT promoter methylation and temozolomide response in choroid plexus carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=4646190&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl48v7nk1752m8644%2F</link>
            <description>We report a 38-year-old man with CPC in the lateral ventricle
 with obstructive hydrocephalus. Because of the poor demarcation between thalamus and fornix, subtotal tumor resection was
 performed. Postoperative spine magnetic resonance (MR) image revealed whole spinal axis dissemination. After diagnosis of
 CPC, the patient was treated with whole ventricular and spine radiation concomitant with temozolomide chemotherapy, although
 the O
 6-methylguanine-DNA methyltransferase (MGMT) promoter was found to be unmethylated. Although MR images revealed transient stable
 disease during adjuvant therapy, tumor progression was depicted after four cycles of temozolomide therapy. We discuss the
 ineffectiveness of adjuvant temozolomide therapy for CPC in connection with O
 6-methylguanine-DNA methyl...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4646190</comments>
            <pubDate>Fri, 25 Mar 2011 18:50:32 +0100</pubDate>
            <guid isPermaLink="false">4646190</guid>        </item>
        <item>
            <title>Brain metastases exhibit gross deletions of the APC gene</title>
            <link>http://www.medworm.com/index.php?rid=4646189&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5j24425154u4j033%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Candidate genes involved in metastasis to the brain require investigation. In the present study, the adenomatous polyposis
 coli (APC) gene was analyzed in a set of human brain metastases. Gross deletions of the APC gene were tested by polymerase chain reaction/loss of heterozygosity (LOH) using the restriction fragment length polymorphism
 method performed by the use of MspI and RsaI genetic markers inside exon 15 and exon 11. Among 21 brain metastases analyzed, 58.8% of samples showed LOH of the APC gene. When assigning the genetic changes to a specific primary tumor type, 6 LOHs were found in metastases originated from
 lung and 4 LOHs in metastases from colon. The main effector of the wnt signaling, beta-catenin, was upregulated in 42.9% of
 cases and transferred to...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4646189</comments>
            <pubDate>Fri, 25 Mar 2011 18:50:32 +0100</pubDate>
            <guid isPermaLink="false">4646189</guid>        </item>
        <item>
            <title>Mixed germ cell tumor and hemangioblastoma in the cerebellum: report of a rare coexistence</title>
            <link>http://www.medworm.com/index.php?rid=4646192&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb3652j81m3742286%2F</link>
            <description>We report a case of a cerebellar tumor consisting of a mixed germ cell tumor (GCT) and a hemangioblastoma. A 22-year-old man
 presented with myoclonus and cerebellar ataxia. Magnetic resonance imaging showed a tumor mass in the left cerebellar hemisphere.
 The tumor was totally removed, and the histological diagnosis was an undetermined neoplasm. Ten months later, the patient
 returned with cerebellar hemorrhage at the site of the previous tumor. An emergency craniotomy was performed, and a tumor
 mass adjacent to the hematoma was resected. Microscopic examination revealed a mixed GCT consisting of a germinoma, choriocarcinoma,
 and mature teratomatous component. An area of hemangioblastoma was also found in the same tumor mass. A retrospective examination
 of the histological sample from ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4646192</comments>
            <pubDate>Fri, 25 Mar 2011 18:50:30 +0100</pubDate>
            <guid isPermaLink="false">4646192</guid>        </item>
        <item>
            <title>Indication of intraoperative immunohistochemistry for accurate pathological diagnosis of brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=4617846&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F752845m4315544v4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Immunohistochemical staining is important for histological diagnosis of brain tumors; however, its intraoperative application
 has rarely been reported. Herein, we describe our methods and four successfully diagnosed cases. Between January 2008 and
 April 2010, intraoperative immunohistochemical analysis was performed in 43 patients undergoing brain tumor surgery at our
 institute. The time for rapid histological diagnosis was 70&amp;nbsp;min. MIB-1 immunostaining was performed; staining index (SI) was
 0.8–76.2% (median, 2.5%) in rapid diagnoses and 0.6–83.9% (median, 7.7%) in permanent diagnoses. There was no discrepancy
 in low- or high-grade tumors between intraoperative and final pathological diagnosis. The antibodies used for staining were
 MIB-1 in all cases, L26...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4617846</comments>
            <pubDate>Thu, 17 Mar 2011 18:34:25 +0100</pubDate>
            <guid isPermaLink="false">4617846</guid>        </item>
        <item>
            <title>Indeterminacy in the WHO classification of tumors: an example of the histopathological diagnosis of brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=4578809&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe8r717411w703k80%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The WHO classifications of tumors are the global standards of tumor diagnosis. In spite of the detailed descriptions of the
 histopathological features of tumors in the classifications, tumors may be difficult to diagnose or the diagnosis can be improper.
 One of the reasons is that the diagnostic criteria have indeterminacy. In this article, we clarify this indeterminacy and
 discuss the diagnostic problems associated with indeterminacy. Indeterminacy of the histopathological features is classified
 according to the following three points: specificity, constancy, and exclusiveness. We consider an oblique (ambiguous description),
 variable (not always present), or duplicative feature as an indeterminate feature. Under indeterminacy, pathologists make
 their diagnosis on...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4578809</comments>
            <pubDate>Fri, 11 Mar 2011 06:51:59 +0100</pubDate>
            <guid isPermaLink="false">4578809</guid>        </item>
        <item>
            <title>Clinicopathological and immunohistochemical study of 20 choroid plexus tumors: their histological diversity and the expression of markers useful for differentiation from metastatic cancer</title>
            <link>http://www.medworm.com/index.php?rid=4576170&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F47710028p1771874%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study was to summarize the clinicopathological features and the histological diversity of choroid plexus tumors
 and to examine the expression of immunohistochemical markers that are useful for their differentiation from metastatic cancer.
 Twenty cases were collected, including 11 choroid plexus papillomas, 5 choroid plexus adenomas, 1 atypical choroid plexus
 papilloma, and 3 choroid plexus carcinomas. The choroid plexus papillomas showed various parenchymal and stromal changes:
 focal solid growth, oncocytic alterations, melanin deposition, calcification, ossification, and xanthogranulomatous reactions.
 The choroid plexus tumors showed the following cytokeratin (CK) 7 and 20 staining patterns: CK7(+)/CK20(+) (11/19 cases),
 CK7(+)/CK20(−) (7/19 cas...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4576170</comments>
            <pubDate>Thu, 10 Mar 2011 17:15:34 +0100</pubDate>
            <guid isPermaLink="false">4576170</guid>        </item>
        <item>
            <title>Detection of IDH1 mutation in human gliomas: comparison of immunohistochemistry and sequencing</title>
            <link>http://www.medworm.com/index.php?rid=4537362&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp432n021g2752hgw%2F</link>
            <description>In conclusion, the anti-IDH1-R132H-specific monoclonal antibody IMab-1 is very useful for detecting IDH1-R132H in
 immunohistochemistry, and predicting the time to progression in grade III anaplastic astrocytomas. Therefore, IMab-1 is likely
 to be useful for the diagnosis of mutation-bearing gliomas and for determining the treatment strategy of grade III gliomas.
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s10014-011-0023-7Authors
		Shingo Takano, Department of Neurosurgery, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8575, JapanWei Tian, Molecular Tumor Marker Research Team, The Oncology Research Center, Advanced Molecular Epidemiology Research Institute, 2-2-2 Iida-nishi, Yamagata, 990-9585 JapanMasahide Matsuda, Department of N...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4537362</comments>
            <pubDate>Thu, 24 Feb 2011 00:08:16 +0100</pubDate>
            <guid isPermaLink="false">4537362</guid>        </item>
        <item>
            <title>Quantitative analysis of matrix metalloproteinase-2 mRNA expression in central and peripheral regions of gliomas</title>
            <link>http://www.medworm.com/index.php?rid=4498946&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg8113502u2012888%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Malignant gliomas are characterized by their invasiveness and angiogenesis. Matrix metalloproteinases (MMPs) degrade extracellular
 matrix and create a more permissive environment for cell invasion. We aimed to investigate for the presence of inter- and
 intratumoral heterogeneity in MMP-2 messenger RNA (mRNA) expression by means of quantitative analysis and to evaluate its
 prognostic impact in glioma patients. Representative sections from the center and periphery of tumors resected en bloc were
 taken fresh for study, stained with hematoxylin/eosin for histological evaluation, and immunohistochemically analyzed for
 Ki-67. MMP-2 mRNA expression was evaluated by real-time reverse transcriptase polymerase chain reaction (RT-PCR). There was
 MMP-2 expression in all analy...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4498946</comments>
            <pubDate>Fri, 18 Feb 2011 06:50:07 +0100</pubDate>
            <guid isPermaLink="false">4498946</guid>        </item>
        <item>
            <title>O6-Methylguanine DNA methyltransferase expression in tumor cells predicts outcome of radiotherapy plus concomitant and adjuvant temozolomide therapy in patients with primary glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=4498948&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp864735530xj34m4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Expression of the O6-methylguanine-DNA methyltransferase (MGMT) gene has been shown to correlate with clinical outcomes in patients with glioblastoma
 multiforme treated with alkylating agents. We evaluated MGMT protein expression in 53 primary glioblastomas by the immunohistochemistry
 (IHC) and analyzed the correlation between results of immunostaining and patient outcomes. There were 28 MGMT-immunopositive
 and 25 negative glioblastomas. Patients with MGMT-immunonegative glioblastomas showed significantly longer progression-free
 survival (PFS) (P&amp;nbsp;=&amp;nbsp;0.0032), but no statistically significant benefits on overall survival (OS) (P&amp;nbsp;=&amp;nbsp;0.0825) were shown. In 41 glioblastomas treated with temozolomide (TMZ) therapy (MGMT-immunopositive: n&amp;nbsp;=&amp;nbsp;22, ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4498948</comments>
            <pubDate>Fri, 18 Feb 2011 06:50:05 +0100</pubDate>
            <guid isPermaLink="false">4498948</guid>        </item>
        <item>
            <title>Non-promoter hypermethylation of zygote arrest 1 (ZAR1) in human brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=4498947&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy8722235537pm815%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Zygote arrest 1 (ZAR1) is a novel maternal-effect gene of crucial importance during the oocyte-to-embryo transition. Comprehensive methylation
 analysis of tumor-specific differently methylated regions in human malignant melanomas has recently led to the identification
 of non-promoter hypermethylation of the ZAR1 gene that had never been identified as an aberrant methylated region in any human tumor. Notably, ZAR1 hypermethylation was frequently observed in melanomas but was absent in benign nevi, and ZAR1 expression was found to be
 up-regulated in methylated tumors. These findings prompted us to screen for ZAR1 non-promoter methylation in various types of human brain tumors using MassARRAY EpiTYPER. Strikingly, hypermethylation of
 ZAR1 was observed frequently in d...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4498947</comments>
            <pubDate>Fri, 18 Feb 2011 06:50:05 +0100</pubDate>
            <guid isPermaLink="false">4498947</guid>        </item>
        <item>
            <title>Epstein–Barr virus (EBV)-associated primary central nervous system lymphoma: is incidence of EBV expression associated with median survival time?</title>
            <link>http://www.medworm.com/index.php?rid=4491712&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F287v647263878674%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The frequency and clinical features of Epstein–Barr virus (EBV)-associated primary central nervous system lymphoma (PCNSL)
 in elderly patients were investigated in this study. Thirty-three PCNSL cases were enrolled in the retrospective study. Biopsies
 were performed, and tissue was embedded in paraffin and sectioned. In-situ hybridization of EBV-encoded small RNAs was then
 conducted. Specimens were scored as having one of three possible results: negative (no EBV-positive cells), slightly positive
 (&amp;lt;50% EBV-positive cells), and strongly positive (&amp;gt;50% EBV-positive cells). Fifteen cases were negative for EBV expression.
 Sixteen cases were slightly positive, and two cases (68 and 79&amp;nbsp;years of age) were strongly positive. The incidence of strongly
 positive...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4491712</comments>
            <pubDate>Wed, 16 Feb 2011 07:01:52 +0100</pubDate>
            <guid isPermaLink="false">4491712</guid>        </item>
        <item>
            <title>Olig2 is useful in the differential diagnosis of oligodendrogliomas and extraventricular neurocytomas</title>
            <link>http://www.medworm.com/index.php?rid=4467335&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F75448748681681r7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 42-year-old woman had suffered from headaches since April 2009. Computed tomography revealed a tumor with marked calcification
 in the left frontal lobe adjacent to the left anterior horn of the lateral ventricle. T1-weighted gadolinium-enhanced magnetic
 resonance imaging showed a well-enhanced tumor at the lesion. Dynamic methionine positron emission tomography showed no delayed
 methionine attenuation. Initial preoperative diagnosis was extraventricular neurocytoma (EVN). However, oligodendroglioma
 was determined upon a second diagnosis. The patient underwent total tumor removal. Hematoxylin and eosin staining showed the
 characteristic fried egg-like cells, round nuclei, and immunohistochemically, the tumor cells were positive for glial fibrillary
 acidic protein...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4467335</comments>
            <pubDate>Thu, 10 Feb 2011 19:58:56 +0100</pubDate>
            <guid isPermaLink="false">4467335</guid>        </item>
        <item>
            <title>Angiogenesis in meningiomas</title>
            <link>http://www.medworm.com/index.php?rid=4440056&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyr14047167834552%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Neoangiogenesis has been correlated to biological aggressiveness and an adverse clinical course of several neoplasias. Its
 prognostic role in meningiomas appears to be controversial. Nonetheless, if adequately quantified with specific markers and
 appropriate scoring methods, angiogenesis seems to be significantly associated with a high growth fraction, development of
 recurrences and shorter overall survival of meningiomas. As a consequence, neoangiogenesis may represent a target for therapies
 aimed at reducing the growth of inoperable meningiomas or recurrence risk of totally resected tumors. Even more significantly,
 the identification of the factors that mediate angiogenesis in meningiomas could help us to determine appropriate novel anti-angiogenic
 therapies for...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4440056</comments>
            <pubDate>Thu, 03 Feb 2011 22:03:54 +0100</pubDate>
            <guid isPermaLink="false">4440056</guid>        </item>
        <item>
            <title>Pineal mixed germ cell tumor with a synchronous sellar lesion in the sixth decade</title>
            <link>http://www.medworm.com/index.php?rid=4440057&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa8254755655l0551%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intracranial germ cell tumors (GCTs) typically affect children and adolescents. We here report on a 59-year-old male patient
 presenting with diplopia, polydipsia and polyuria. On clinical examination, slight restriction of the upward gaze was seen
 on the left side. Computed tomography demonstrated calcifications in the pineal region and enhanced neurohypophysis. Magnetic
 resonance imaging displayed a heterogeneous pineal mass of 3-cm diameter, which was multicystic with an enhanced cyst wall,
 and also swelling of the pituitary stalk. The pineal lesion of the tumor, which included calcifications and keratinaceous
 components, was totally excised using an occipital transtentorial approach. Histopathological examination showed it to be
 a mixed GCT with germinoma and m...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4440057</comments>
            <pubDate>Thu, 03 Feb 2011 07:06:02 +0100</pubDate>
            <guid isPermaLink="false">4440057</guid>        </item>
        <item>
            <title>Glioma-initiating cells and molecular pathology: implications for therapy</title>
            <link>http://www.medworm.com/index.php?rid=4430230&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq36u6g1343007704%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There is now compelling evidence that gliomas harbor a small population of cells, termed glioma-initiating cells (GICs), characterized
 by their ability to undergo self-renewal and initiate tumorigenesis. The development of therapeutic strategies targeted toward
 GIC signaling may improve the treatment of malignant gliomas. The characterization of GICs provides a clue to elucidating
 histological heterogeneity and treatment failure. The role of the stem cell marker CD133 in the initiation and progression
 of brain tumors is still uncertain. Here, we review some of the signaling mechanisms involved in GIC biology, such as phosphatase
 and tensin homolog (PTEN), sonic hedgehog, Notch, and WNT signaling pathways, maternal embryonic leucine-zipper kinase (MELK),
 BMI1, and ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4430230</comments>
            <pubDate>Thu, 27 Jan 2011 17:40:33 +0100</pubDate>
            <guid isPermaLink="false">4430230</guid>        </item>
        <item>
            <title>Quantitative digital assessment of MGMT immunohistochemical expression in glioblastoma tissue</title>
            <link>http://www.medworm.com/index.php?rid=4383934&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1601745737563675%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recent reports have suggested an important clinical role for hypermethylation of the O6-methylguanine-DNA-methyltransferase (MGMT) promoter in patients with glioblastomas. Whether MGMT protein expression is correlated
 with promoter hypermethylation and patient outcomes, however, has not been elucidated. Here we describe a quantitative digital
 method for assessment of MGMT-specific immunostaining, and analyze the relationship between expression levels and methylation
 status of the MGMT promoter. We investigated 46 tumors from patients who received a diagnosis of glioblastoma or gliosarcoma.
 Immunohistochemistry with anti-MGMT antibody and methylation-specific PCR using bisulfite-modified tumor DNA were performed.
 The digital assessment method used image-analysis sof...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4383934</comments>
            <pubDate>Wed, 19 Jan 2011 13:43:01 +0100</pubDate>
            <guid isPermaLink="false">4383934</guid>        </item>
        <item>
            <title>Histopathological study of spinal meningioma originating from the arachnoid villi</title>
            <link>http://www.medworm.com/index.php?rid=4339916&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl21043r0k7m2175x%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although the histogenesis of meningiomas remains unclear, it is believed that arachnoid cells are the most likely origin of
 this type of neoplasm. Further, little attention has been paid to the histopathology of spinal meningiomas arising from the
 arachnoid villi. We came across a case of spinal meningioma that was locally attached to the arachnoid membrane. The associated
 arachnoid villi were investigated by light microscopy and immunohistochemical analysis. We confirmed the presence of tumor
 cells under the fibrous capsule that forms the outer component of the arachnoid villi. Tumor cells grew out from the apical
 portion of the arachnoid villi. Furthermore, immunohistochemical study suggested that arachnoid cells made the transition
 to tumor cells on the arachno...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4339916</comments>
            <pubDate>Mon, 10 Jan 2011 15:52:36 +0100</pubDate>
            <guid isPermaLink="false">4339916</guid>        </item>
        <item>
            <title>Angiogenesis and invasion in glioma</title>
            <link>http://www.medworm.com/index.php?rid=4327992&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa7812p4155r54838%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Despite advances in surgical and medical therapy, glioblastoma consistently remains a fatal disease. Over the last 20&amp;nbsp;years,
 no significant increase in survival has been achieved for patients with this disease. The formation of abnormal tumor vasculature
 and glioma cell invasion along white matter tracts are believed to be the major factors responsible for the resistance of
 these tumors to treatment. Therefore, investigation of angiogenesis and invasion in glioblastoma is essential for the development
 of a curative therapy. In our report, we first reviewed certain histopathological studies that focus on angiogenesis and invasion
 of human malignant gliomas. Second, we considered several animal models of glioma available for studying angiogenesis and
 invasion, ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4327992</comments>
            <pubDate>Fri, 07 Jan 2011 14:51:25 +0100</pubDate>
            <guid isPermaLink="false">4327992</guid>        </item>
        <item>
            <title>High-throughput immunohistochemical profiling of primary brain tumors and non-neoplastic systemic organs with a specific antibody against the mutant isocitrate dehydrogenase 1 R132H protein</title>
            <link>http://www.medworm.com/index.php?rid=4325274&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn72t6221m50r3x04%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Isocitrate dehydrogenase 1 (IDH1) mutations are common in grade II–III diffuse gliomas and secondary glioblastomas. The aim
 of this study is to investigate the staining pattern of mIDH1R132H, an antibody specific to mutant IDH1 protein, in primary
 brain tumors and non-neoplastic systemic organs. Eight of 13 diffuse astrocytomas, 1 of 6 anaplastic astrocytomas, 9 of 11
 oligodendrogliomas, 15 of 22 anaplastic oligodendrogliomas, 6 of 7 oligoastrocytomas, and 5 of 8 anaplastic oligoastrocytomas
 showed both cytoplasmic and nuclear positivity. Two of 25 atypical meningiomas and 2 of 42 pituitary adenomas were positive
 for mIDH1R132H. The following non-neoplastic systemic organs showed positivity in the cytoplasm alone: the myocardium, peribronchial
 glands, interlobul...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4325274</comments>
            <pubDate>Thu, 06 Jan 2011 17:56:51 +0100</pubDate>
            <guid isPermaLink="false">4325274</guid>        </item>
        <item>
            <title>Rhabdoid glioblastoma in a child: case report and literature review</title>
            <link>http://www.medworm.com/index.php?rid=4325275&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmn672269282q2g53%2F</link>
            <description>We report a case
 of rhabdoid glioblastoma in a 12-year-old boy who presented with headache and harbored a 70-mm solid tumor in the left temporal
 lobe. The tumor was surgically excised, but early tumor recurrence and leptomeningeal spread developed, and the patient died
 of the disease 4.9&amp;nbsp;months after surgery. Histologically, the tumor contained two distinct patterns of glioblastoma and rhabdoid
 cells with necrosis and hemorrhage. Immunohistochemical analysis revealed that both cells were positive for glial fibrillary
 acid protein, vimentin, and INI1, which is consistent with the reported diagnosis of rhabdoid glioblastoma. Genetic studies
 confirmed no loss of the INI1 gene and identified hemizygous deletion of 
 the CDKN2A gene. We review reported cases of rhabdoid glioblastoma ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4325275</comments>
            <pubDate>Thu, 06 Jan 2011 17:56:50 +0100</pubDate>
            <guid isPermaLink="false">4325275</guid>        </item>
        <item>
            <title>Persistent roles of signal transduction of platelet-derived growth factor B in genesis, growth, and anaplastic transformation of gliomas in an in-vivo serial transplantation model</title>
            <link>http://www.medworm.com/index.php?rid=4319654&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F836134q164633p24%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We previously reported that retrovirally transduced platelet-derived growth factor-B (PDGFB) in glial progenitors of the rat
 cerebral white matter, subventricular zone, or brain stem induced malignant brain tumors closely resembling human glioblastoma
 (GBM). While human GBMs may progress over the period of several months to a few years, prospective, long-term in-vivo observation
 of histological changes of the tumor tissues is not feasible in these models, because the animals undergo rapid tumor progression
 and mortality within approximately 1&amp;nbsp;month. We thus performed successive, long-term in-vivo transplantation of the PDGFB-induced
 tumor cells into the rat cerebrum. Primary retroviral transduction of PDGFB in the glial progenitors of the rat basal ganglia
 in...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4319654</comments>
            <pubDate>Wed, 05 Jan 2011 16:52:09 +0100</pubDate>
            <guid isPermaLink="false">4319654</guid>        </item>
        <item>
            <title>Spontaneous regression of multicentric pilocytic astrocytoma with CSF dissemination in an adult</title>
            <link>http://www.medworm.com/index.php?rid=4319653&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq082jp43r480r004%2F</link>
            <description>We present a case of spontaneous regression of multicentric pilocytic astrocytoma with cerebrospinal fluid (CSF) dissemination
 without neurofibromatosis type 1 (NF1) in an adult, the first such case reported. Magnetic resonance imaging (MRI) showed
 multiple low signal intensity lesions on T1-weighted images and high signal intensity areas on T2-weighted images in the bilateral
 thalamus, basal ganglia and midbrain. Contrast-enhanced MRI revealed that small, enhanced lesions were seen in the basal ganglia
 and the pineal region. Neuroendoscopic biopsy and third ventriculostomy were performed. Intraoperative findings demonstrated
 CSF dissemination. Histologically, the specimens showed pilocytic astrocytoma. Serial MRIs showed regression of the tumor
 without any additional treatment. The ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4319653</comments>
            <pubDate>Wed, 05 Jan 2011 16:52:09 +0100</pubDate>
            <guid isPermaLink="false">4319653</guid>        </item>
        <item>
            <title>Infratentorial brain metastases of pediatric non-epithelial malignant tumors: three case reports</title>
            <link>http://www.medworm.com/index.php?rid=4319652&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1525463077751483%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Three pediatric patients with infratentorial metastatic non-epithelial malignant brain tumors were successfully treated by
 radical surgical resection followed by aggressive radiochemotherapy. One patient with neuroblastoma and two with rhabdomyosarcoma
 were successfully treated by first line multimodal treatments, but developed infratentorial metastasis after several months
 of remission. All patients revealed intracranial metastases manifesting as rapidly progressing neurological symptoms caused
 by mass effect in the posterior fossa. Radical surgical resection was performed without morbidity. The patients were then
 treated by adjuvant radiochemotherapy with or without autologous peripheral blood stem cell transplantation, resulting in
 complete remission. Two patie...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4319652</comments>
            <pubDate>Wed, 05 Jan 2011 16:52:09 +0100</pubDate>
            <guid isPermaLink="false">4319652</guid>        </item>
        <item>
            <title>Primary central nervous system lymphoma in acquired immune deficiency syndrome mimicking toxoplasmosis</title>
            <link>http://www.medworm.com/index.php?rid=4319655&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0t4121145767575l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 37-year-old man, a hepatitis B virus carrier due to mother-to-child transmission, had a medical examination in September
 2008 in nearby hospitals due to anorexia and weight loss. He was transported to our hospital because computed tomography (CT)
 detected intracranial lesions, and he had a positive human immunodeficiency virus (HIV) antibody test. Head computed tomography
 (CT) revealed multiple hemorrhagic lesions and enhancement effect, suggesting a thin wall. Also, an enhancement effect was
 present in the ventricle walls and the subarachnoid space. No accumulation was found in the thallium-201 scintigraphy. The
 enhancement effect of the ventricle walls and the subarachnoid space disappeared after oral administration of pyrimethamine,
 sulfadiazine, and calcium ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4319655</comments>
            <pubDate>Wed, 05 Jan 2011 16:52:08 +0100</pubDate>
            <guid isPermaLink="false">4319655</guid>        </item>
        <item>
            <title>CXCL12/CXCR4 signaling in malignant brain tumors: a potential pharmacological therapeutic target</title>
            <link>http://www.medworm.com/index.php?rid=4319657&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7210601159570t04%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chemokines are 8- to 12-kDa peptides that function as chemoattractant cytokines involved in cell activation, differentiation,
 and trafficking. Chemokines bind to specific G-protein-coupled, seven-span transmembrane receptors on the plasma membrane
 of target cells. Chemokine (C-X-C motif) ligand 12 (CXCL12), an alpha-chemokine that binds to G-protein-coupled chemokine
 (C-X-C motif) receptor 4 (CXCR4), plays an important and unique role in the regulation of stem/progenitor-cell trafficking.
 As CXCR4 is expressed on several cancer cells, these CXCR4-positive cancer cells may metastasize to organs that secrete/express
 CXCL12. Regarding brain tumors, recent data demonstrate that glioma tumor stem-like cells promote tumor angiogenesis and vasculogenesis
 via the CXCL12/C...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4319657</comments>
            <pubDate>Wed, 05 Jan 2011 16:52:07 +0100</pubDate>
            <guid isPermaLink="false">4319657</guid>        </item>
        <item>
            <title>Subependymal giant cell astrocytoma with oncocytic change</title>
            <link>http://www.medworm.com/index.php?rid=4319656&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff105732752723856%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 49-year-old woman presented with a history of periodic episodes of nausea and vomiting starting in 2006. In June 2009, the
 patient lost consciousness and was transported to our hospital. Head computed tomography (CT) revealed hydrocephalus caused
 by an enhancing mass lesion with calcification located in the right lateral ventricle around the foramen of Monro. Total tumor
 removal was performed. Histologic findings revealed fibrillated spindle tumor cells and giant tumor cells with abundant cytoplasm.
 The spindle tumor cells were immunoreactive for GFAP and S-100 protein, but none of the giant tumor cells were immunoreactive
 for GFAP or S-100 protein. Electron microscopic examination revealed abundant mitochondria in the tumor cell cytoplasm. According
 to these fi...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4319656</comments>
            <pubDate>Wed, 05 Jan 2011 16:52:07 +0100</pubDate>
            <guid isPermaLink="false">4319656</guid>        </item>
        <item>
            <title>Precise comparison of protoporphyrin IX fluorescence spectra with pathological results for brain tumor tissue identification</title>
            <link>http://www.medworm.com/index.php?rid=4301250&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft1h4227w2278764v%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Photodynamic diagnosis is used during glioma surgery. Although some studies have shown that the spectrum of fluorescence was
 efficient for precise tumor diagnosis, previous methods to characterize the spectrum have been problematic, which can lead
 to misdiagnosis. In this paper, we introduce a comparison technique to characterize spectrum from pathology and results of
 preliminary measurement using human brain tissues. We developed a spectrum scanning system that enables spectra measurement
 of raw tissues. Because tissue preparations retain the shape of the device holder, spectra can be compared precisely with
 pathological examination. As a preliminary analysis, we measured 13 sample tissues from five patients with brain tumors. The
 technique enabled us to measure ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4301250</comments>
            <pubDate>Tue, 28 Dec 2010 15:14:00 +0100</pubDate>
            <guid isPermaLink="false">4301250</guid>        </item>
        <item>
            <title>Epithelioid glioblastoma changed to typical glioblastoma: the methylation status of MGMT promoter and 5-ALA fluorescence</title>
            <link>http://www.medworm.com/index.php?rid=4301251&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2x00835653141186%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 55-year-old man was admitted to our hospital complaining of left hemiparesis. Magnetic resonance imaging (MRI) showed a
 smooth ring-like enhanced cystic tumor in the right parietal lobe. He underwent gross total resection of the tumor under neuronavigation
 and 5-aminolevulinic acid (5-ALA) fluorescence guiding method. Histopathological examination of the tumor showed small cells
 formed epithelioid solid nests with some focus of duct-like structure. On the basis of the MRI and operative and histological
 findings, this tumor was diagnosed as a metastatic poorly differentiated carcinoma, although the primary cancer could not
 be detected by metastatic work-ups. Afterward, this tumor recurred repeatedly. Histopathological examination of specimen from
 the fourth surge...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4301251</comments>
            <pubDate>Tue, 28 Dec 2010 15:13:59 +0100</pubDate>
            <guid isPermaLink="false">4301251</guid>        </item>
        <item>
            <title>A case of atypical teratoid/rhabdoid tumor in an adult, with long survival</title>
            <link>http://www.medworm.com/index.php?rid=4288066&amp;cid=s_33459_32_f&amp;fid=35912&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpr005258v1m74270%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Atypical teratoid/rhabdoid tumor (AT/RT) is a malignant tumor that mostly occurs in early childhood and has poor prognosis
 despite aggressive therapy. Adult cases are rare and, as far as we are aware, only 30 cases have been reported to date. Here
 we present the case of a 27-year-old female with left parietal AT/RT with the chief complaint of numbness of the right superior
 limb. First, the tumor was surgically removed and the diagnosis was grade II glioma. With additional radiotherapy, the clinical
 course after surgery was favorable. After 6&amp;nbsp;years, she had an operation for recurrence and the diagnosis was grade III glioma.
 Temozolomide was prescribed, and a disease-free period of 2&amp;nbsp;years followed. Surgery was performed for a third time for second
 recurre...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4288066</comments>
            <pubDate>Wed, 22 Dec 2010 20:21:46 +0100</pubDate>
            <guid isPermaLink="false">4288066</guid>        </item>
        <item>
            <title>A cystic meningioma misdiagnosed as malignant glioma by radiologic and intraoperative histological examinations</title>
            <link>http://www.medworm.com/index.php?rid=4141515&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3217667146182466%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cystic meningiomas are radiologically difficult to differentiate from malignant brain tumors, particularly when the tumors
 are intraparenchymally located. In such cases, a surgical strategy relies on intraoperative histological diagnosis. A 60-year-old
 man had a tumor with multiple cysts in the left parietal lobe that was diagnosed radiologically as malignant glioma. In operative
 findings, there was no dural attachment of the tumor, and the border between the tumor and normal brain tissue was unclear.
 Intraoperative histological examination supported the diagnosis of malignant glioma based on a high cellularity and an existence
 of a multinuclear giant cell in the tumor tissue. We finished the surgery with partial tumor resection; however, postoperative
 histologica...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141515</comments>
            <pubDate>Tue, 02 Nov 2010 17:37:05 +0100</pubDate>
            <guid isPermaLink="false">4141515</guid>        </item>
        <item>
            <title>p53 abnormality and tumor invasion in patients with malignant astrocytoma</title>
            <link>http://www.medworm.com/index.php?rid=4141517&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj6pt448t4280gl9m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Malignant astrocytomas are characterized by diffusely infiltrating nature, and the abnormality of p53 is a cytogenetic hallmark
 of astrocytic tumors. To elucidate the relationship between p53 abnormality and invasiveness of the tumors, we studied mutation
 and protein expression of p53 in 48 consecutive patients with malignant astrocytoma (14 anaplastic astrocytomas and 34 glioblastoma
 multiformes). The tumors were classified into three categories according to the features of magnetic resonance imaging, and
 5, 7, and 36 tumors were classified into diffuse, multiple, and single type, respectively. We then examined how these tumor
 types correlate with MIB-1 staining index, TP53 gene mutation, and p53 protein expression. We found that p53 immunopositivity or TP53 mutat...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141517</comments>
            <pubDate>Tue, 02 Nov 2010 17:37:04 +0100</pubDate>
            <guid isPermaLink="false">4141517</guid>        </item>
        <item>
            <title>Radiation-induced osteosarcomas after treatment for frontal gliomas: a report of two cases</title>
            <link>http://www.medworm.com/index.php?rid=4141516&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft511358j95n42307%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Most radiation-induced osteosarcomas of the skull are reported to arise in the facial bone or paranasal sinus after radiotherapy
 for retinoblastoma and/or pituitary adenoma. Here we report two cases of radiation-induced osteosarcoma in the paranasal sinus
 after treatment for frontal glioma. Case 1 was a 56-year-old woman who underwent surgical resection of a left frontal tumor
 in October 1990. The histological diagnosis was a low-grade glioma, and radiotherapy of 54 Gy was administered. Sixteen years
 later, in September 2006, the patient noted an enlarging subcutaneous mass in the right frontal region. CT showed an osteolytic
 mass in the right frontal sinus. An open biopsy established the histopathological diagnosis of osteosarcoma, and the patient
 subsequently di...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141516</comments>
            <pubDate>Tue, 02 Nov 2010 17:37:04 +0100</pubDate>
            <guid isPermaLink="false">4141516</guid>        </item>
        <item>
            <title>Ectopic adrenal cortical adenoma in the spinal region: case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=4141518&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhl32651477026j77%2F</link>
            <description>We report a 17-month-old
 girl with spinal adrenal cortical neoplasms. She was unable to crawl or stand and was irritable at night. Her appearance was
 asymmetrical; the right side of her face and her lower right leg were enlarged. In addition, she manifested hyperplasia of
 the thymus, fibrous hyperplasia of the bladder, and hamartoma in the liver. However, all abnormalities were asymptomatic.
 Magnetic resonance imaging (MRI) revealed well-circumscribed masses within the dura mater at the T12-L1 and L3-L4 level. Histology
 disclosed that the lesions were composed of sheets and nests of round and polygonal cells with mostly round regular nuclei;
 eosinophilic to clear cytoplasm was abundant. Immunohistochemically, the tumor cells were strongly positive for inhibin-alpha,
 positive for syn...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141518</comments>
            <pubDate>Tue, 02 Nov 2010 17:37:03 +0100</pubDate>
            <guid isPermaLink="false">4141518</guid>        </item>
        <item>
            <title>Intra-axial pseudotumors in the central nervous system: clinicopathological analysis</title>
            <link>http://www.medworm.com/index.php?rid=4141520&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1335k6801621685q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intra-axial pseudotumors in the central nervous system often mimic malignant brain tumors and cause difficulty in diagnosis
 and treatment. The present study investigates their radiologic and histological features to elucidate diagnostic clues. Six
 cases were included in the study, one man and five women, ranging in age from 44 to 87 years (mean age, 61 years). Histologically,
 three cases had demyelination, and one case each had abscess, angiitis, and non-Langerhans cell histiocytosis. All cases were
 evaluated radiologically on MRI, most of them by thallim-201 single photon emission tomography (201Tl-SPECT). These cases were examined using H&amp;E, special stains, and immunohistochemical studies with a variety of antibodies.
 MRI demonstrated perifocal edema and ring-lik...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141520</comments>
            <pubDate>Tue, 02 Nov 2010 17:37:02 +0100</pubDate>
            <guid isPermaLink="false">4141520</guid>        </item>
        <item>
            <title>Morphological and flow cytometric analysis of cell infiltration in glioblastoma: a comparison of autopsy brain and neuroimaging</title>
            <link>http://www.medworm.com/index.php?rid=4141519&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9516514u72412172%2F</link>
            <description>We examined seven autopsy brains, focusing on tumor cell infiltration in the peripheral zone of a tumor, and compared our
 findings with the MR images. There has so far been no report regarding mapping of tumor cell infiltration and DNA histogram
 by flow cytometry, comparing the neuroimaging findings with the autopsy brain findings. The autopsy brain was cut in 10-mm-thick
 slices, in parallel with the OM line. Tissue samples were obtained from several parts in the peripheral zone (the outer area
 adjacent to the tumor edge as defined by postcontrast MRI) and then were examined by H&amp;E, GFAP, and VEGF staining. We defined
 three infiltrating patterns based on number of infiltrated cells as follows: A zone, 100%–60% of the cells infiltrated tumor
 cells compared with tumor cell density of...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141519</comments>
            <pubDate>Tue, 02 Nov 2010 17:37:02 +0100</pubDate>
            <guid isPermaLink="false">4141519</guid>        </item>
        <item>
            <title>Proton magnetic resonance spectroscopic imaging in pediatric low-grade gliomas</title>
            <link>http://www.medworm.com/index.php?rid=4141521&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg6m8449mt1735340%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Our purpose was to investigate whether in vivo proton magnetic resonance spectroscopic imaging, using normalized concentrations
 of total choline (tCho) and total creatine (tCr), can differentiate between WHO grade I pilocytic astrocytoma (PA) and diffuse,
 fibrillary WHO grade II astrocytoma (DA) in children. Data from 16 children with astrocytomas (11 children with PA and 5 children
 with DA) were evaluated retrospectively. MRS was performed before treatment in all patients with histologically proven low-grade
 astrocytomas. Metabolite concentrations of tCho and tCr were normalized to the respective concentration in contralateral brain
 tissue. The Mann-Whitney U test was performed to evaluate differences between these two groups. Normalized tCho did not show any stat...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141521</comments>
            <pubDate>Tue, 02 Nov 2010 17:37:01 +0100</pubDate>
            <guid isPermaLink="false">4141521</guid>        </item>
        <item>
            <title>A rare case of a simultaneously detected suprasellar and intramedullary spinal cord germinoma</title>
            <link>http://www.medworm.com/index.php?rid=4141522&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0184uq324414n241%2F</link>
            <description>This article describes
 a rare case of simultaneously detected intracranial and intramedullary spinal cord germinoma and its possible etiopathology.
 
 
	Content Type Journal ArticleDOI 10.1007/s10014-010-0269-5Authors
		Carter S. Rabo, Department of Neurosurgery, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka, 565-0871 JapanNaoya Hashimoto, Department of Neurosurgery, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka, 565-0871 JapanNaoki Kagawa, Department of Neurosurgery, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka, 565-0871 JapanToshiaki Fujita, Department of Neurosurgery, Osaka Koseinenkin Hospital, Osaka, JapanRyuichi Hirayama, Department of Neurosurgery, Osaka Koseinenkin Hospital, Osaka, JapanHideo O...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141522</comments>
            <pubDate>Tue, 02 Nov 2010 17:37:00 +0100</pubDate>
            <guid isPermaLink="false">4141522</guid>        </item>
        <item>
            <title>Epileptogenic glioma in a 4-year-old child: a case report</title>
            <link>http://www.medworm.com/index.php?rid=4141524&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx73726561hh8nx28%2F</link>
            <description>We report a rare case of epileptogenic glioma composed of glial progenitor cells that differentiated into an astrocytic and
 oligodendrocytic tumor. This 4-year-old girl presented with a 1-year history of complex partial seizure. MR scan showed a
 mass in the left temporal lobe with a cyst and a contrast-enhanced component. Subtotal resection of the tumor was achieved.
 Histological examination revealed that the tumor exhibited low cellularity composed of astrocytic and oligodendrocytic components,
 as well as low mitotic activity (MIB-1 = 1%). Immunohistochemical examination revealed GFAP positivity within the astrocytic
 cells, olig2 positivity within the oligodendrocytic cells, and S100 positivity in both cell types. MAP2 and CD34 were negative,
 and neurofilament was only positive in p...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141524</comments>
            <pubDate>Tue, 02 Nov 2010 17:36:59 +0100</pubDate>
            <guid isPermaLink="false">4141524</guid>        </item>
        <item>
            <title>Detection of failure of bevacizumab treatment for malignant glioma based on urinary matrix metalloproteinase activity</title>
            <link>http://www.medworm.com/index.php?rid=4141523&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffw72372v824m6k85%2F</link>
            <description>In this study, we detected failure of bevacizumab treatment for malignant glioma through upregulation of metalloproteinase
 activity in the urine, as well as infiltrative tumors on MRI. In addition, MMP9 has been proved as a molecule that facilitates
 its infiltrative behavior in vivo in the brain animal model.
 
 
	Content Type Journal ArticleDOI 10.1007/s10014-010-0271-yAuthors
		Shingo Takano, Department of Neurosurgery, Institute of Clinical Medicine, Tennodai, Tsukuba, Ibaraki, 305-8575 JapanRyota Mashiko, Department of Neurosurgery, Institute of Clinical Medicine, Tennodai, Tsukuba, Ibaraki, 305-8575 JapanSatoru Osuka, Department of Neurosurgery, Institute of Clinical Medicine, Tennodai, Tsukuba, Ibaraki, 305-8575 JapanEiichi Ishikawa, Department of Neurosurgery, Institute of Clinica...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141523</comments>
            <pubDate>Tue, 02 Nov 2010 17:36:59 +0100</pubDate>
            <guid isPermaLink="false">4141523</guid>        </item>
        <item>
            <title>Primary central nervous system large B-cell lymphoma with prolific, mixed T-cell and macrophage infiltrates, mimicking multiple sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=3517171&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn272vl352j213164%2F</link>
            <description>We report a 59-year-old man, first diagnosed as
 multiple sclerosis by open biopsy at another institution, who was then correctly diagnosed as PCNSBL after stereotactic biopsy
 at our hospital. The initial biopsy showed heavy lymphoid and macrophage influx with visible demyelination. On rebiopsy, a
 diffuse infiltrate of small to medium-sized lymphocytes was prominent and largely stained as T cells (CD3) by immunohistochemistry.
 There was also an admixture of macrophages, but this time, relatively low numbers of large malignant cells were also identified.
 The latter stained as B cells (CD20), enabling a diagnosis of B-cell lymphoma, and the condition responded fully to high-dose
 methotrexate. It is thus possible for PCNSBL to be histologically misinterpreted as a result of ancillary inf...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517171</comments>
            <pubDate>Wed, 28 Apr 2010 08:30:03 +0100</pubDate>
            <guid isPermaLink="false">3517171</guid>        </item>
        <item>
            <title>Flow cytometric analysis for the mechanism of the new antineoplastic agent temozolomide in glioma cells</title>
            <link>http://www.medworm.com/index.php?rid=3517172&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F633h57lw15l6pm89%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Temozolomide (TMZ) has been accepted as a standard antitumor drug for glioma worldwide. Regarding its mechanism of action,
 there are quite a few analyses. In the present study, we investigated the cell-killing effect and mechanism of action of TMZ
 with flow cytometry using glioblastoma cell lines. Each cell line was divided into three groups: a control group, a low-dose
 TMZ group, and a highdose TMZ group. On day 1, TMZ was added to each cell line. Then, we counted the numbers of cells on days
 2, 3, 4, and 5; in U87MG, we counted the number of cells on days 8 and 9. Simultaneously, we performed flow cytometric analysis
 with single- and double-staining methods. Although results varied slightly depending on the cell line, with flow cytometric
 analysis we identified ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517172</comments>
            <pubDate>Wed, 28 Apr 2010 08:30:02 +0100</pubDate>
            <guid isPermaLink="false">3517172</guid>        </item>
        <item>
            <title>Prognostic value of WT1 protein expression level and MIB-1 staining index as predictor of response to WT1 immunotherapy in glioblastoma patients</title>
            <link>http://www.medworm.com/index.php?rid=3517173&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmn7x78t721l78381%2F</link>
            <description>In conclusion, our study has shown that WT1 protein expression level,
 not MIB-1 staining index, can be used as a prognostic marker to foretell outcome after immunotherapy, and that patients whose
 tumors have intermediate WT1 expression have the best survival outcome.
 
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10014-010-0265-9Authors
		Yasuyoshi Chiba, Osaka University Graduate School of Medicine Department of Neurosurgery 2-2 Yamada-oka Suita, Osaka 565-0871 JapanNaoya Hashimoto, Osaka University Graduate School of Medicine Department of Neurosurgery 2-2 Yamada-oka Suita, Osaka 565-0871 JapanAkihiro Tsuboi, Osaka University Graduate School of Medicine Department of Cancer Immunotherapy Suita JapanCarter Rabo, Osaka University Graduate School of Medicine Depart...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517173</comments>
            <pubDate>Wed, 28 Apr 2010 08:30:01 +0100</pubDate>
            <guid isPermaLink="false">3517173</guid>        </item>
        <item>
            <title>Correlation of MIB-1 staining index and 201Tl-SPECT retention index in preoperative evaluation of malignancy of brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=3517174&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv18710402717t106%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;MIB-1 staining provides a useful index of the malignancy of brain tumors. However, because of the difficulty of evaluating
 malignancy based on the preoperative imaging findings, we investigated the correlation between the 201Tl-SPECT retention index (RI) and MIB-1 staining index (MIB-1 SI) to determine the usefulness of RI for preoperative evaluation
 of the malignancy of brain tumors. The subjects of this study were 47 patients who underwent tumor removal surgery at our
 hospital in 2006 and 2007. The tumors consisted of 16 intraaxial tumors (all gliomas: 9 glioblastomas, 2 anaplastic astrocytomas,
 2 anaplastic oligoastrocytomas, 1 oligodendroglioma, and 2 ependymomas), 8 other malignant brain tumors, and 23 extraaxial
 tumors (10 meningiomas, 7 pituitary adenomas, a...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517174</comments>
            <pubDate>Wed, 28 Apr 2010 08:30:00 +0100</pubDate>
            <guid isPermaLink="false">3517174</guid>        </item>
        <item>
            <title>Expression of podoplanin and calretinin in meningioma: an immunohistochemical study</title>
            <link>http://www.medworm.com/index.php?rid=3517176&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu4387513t1434m10%2F</link>
            <description>We examined the immunohistochemical expression of podoplanin and calretinin, both of which are well-known markers
 of mesothelioma, in 24 surgical cases of meningioma of various types. In most cases, a linear immunoreactivity for podoplanin
 was found along the cell surface of most neoplastic cells. An intracytoplasmic, finely granular, or diffuse immunoreactivity
 was also noted in some cells. These findings corresponded well to immunoreactivity for epithelial membrane antigen (EMA),
 but immunoreactivity for podoplanin was more crisp or sharply delineated and clear compared with that for EMA. These findings
 indicate that podoplanin can be used as an immunohistochemical marker that is equivalent to EMA in the differential diagnosis
 of meningioma. However, most meningiomas did not contai...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517176</comments>
            <pubDate>Wed, 28 Apr 2010 08:29:59 +0100</pubDate>
            <guid isPermaLink="false">3517176</guid>        </item>
        <item>
            <title>Nestin expression in astrocytic tumors delineates tumor infiltration</title>
            <link>http://www.medworm.com/index.php?rid=3517175&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flj02u48546606v41%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Nestin is an intermediate filament protein expressed in undifferentiated cells during central nervous system development,
 and glioma is known to be a highly infiltrative tumor. We determined whether nestin was expressed in astrocytic tumors and
 could identify infiltrating tumor cells. We screened 65 archival, paraffin-embedded adult astrocytic tumors using immunohistochemical
 staining and computerized overlaid photographs. Normal biopsied brains and metastatic brain tumors were also examined. The
 intensity of nestin expression corresponded to the tumor grade. All 33 glioblastoma cases showed positive and extensive staining,
 which was less positive in diffuse astrocytoma. Overlaid images showed that nestin immunostaining delineated tumor invasion
 into adjacent gray...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517175</comments>
            <pubDate>Wed, 28 Apr 2010 08:29:59 +0100</pubDate>
            <guid isPermaLink="false">3517175</guid>        </item>
        <item>
            <title>Melanotic neuroectodermal tumor of the brain recurring 12 years after complete remission: case report</title>
            <link>http://www.medworm.com/index.php?rid=3517178&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3x852018137507u0%2F</link>
            <description>We describe a rare case of melanotic neuroectodermal tumor (MNT) of the brain recurring 12 years after complete remission.
 An 11-year-old girl initially presented with exotropia and bilateral papilledema. Magnetic resonance (MR) imaging revealed
 an intracranial extraaxial large tumor at the midfrontal region. T1-weighted MR imaging showed the tumor to be well delineated with homogeneous enhancement by gadolinium. The tumor was subtotally
 removed, and the histological diagnosis was MNT. The residual tumor became enlarged, so gamma knife radiosurgery was performed
 5 months after initial surgery. The enhanced lesion disappeared, but another lesion emerged 3 years later. A second gamma
 knife radiosurgery was performed for this local recurrence. The enhanced lesion disappeared once again. ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517178</comments>
            <pubDate>Wed, 28 Apr 2010 08:29:58 +0100</pubDate>
            <guid isPermaLink="false">3517178</guid>        </item>
        <item>
            <title>Radiation-induced glioblastoma occurring 35 years after radiation therapy for medulloblastoma: case report</title>
            <link>http://www.medworm.com/index.php?rid=3517177&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbmu0101l67760847%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 41-year-old man was admitted in June 2007 with a 1-month history of headache and cerebellar ataxia. At the age of 5 years,
 in May 1971, he had presented with headache, vomiting, and gait disturbance. Cerebral angiographical study demonstrated vascular
 shift caused by a mass lesion in the cerebellar vermis. He had immediately undergone partial removal. Histological diagnosis
 was medulloblastoma (MB). Postoperatively he received a total of 40 Gy radiation to the whole brain and 30.5 Gy to the spine
 without chemotherapy. He was again seen 35 years later with a radiation-induced glioblastoma (GB) that arose in the region
 of the original MB. The tumor was surgically removed, and he received radiotherapy and chemotherapy with ACNU, procarbazine,
 and vincristine. Posto...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517177</comments>
            <pubDate>Wed, 28 Apr 2010 08:29:58 +0100</pubDate>
            <guid isPermaLink="false">3517177</guid>        </item>
        <item>
            <title>Parasagittal solitary fibrous tumor resembling hemangiopericytoma</title>
            <link>http://www.medworm.com/index.php?rid=3517180&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F28w8p67142648716%2F</link>
            <description>We report the case of a Japanese woman with parasagittal SFT that resembled hemangiopericytoma
 (HPC). Histological examination revealed that the tumor was highly cellular, with cells containing oval- or spindle-shaped
 nuclei arranged in sheets or a pattern-less growth mode. Focal vascular proliferation was also observed. Some areas showed
 intercellular stroma containing remarkable eosinophilic collagens. Tumor cells showed a strong immunoreactivity for CD34 but
 were negative for S-100 protein and epithelial membrane antigen. MIB-1 labeling index of the tumor was 6.6%. Owing to the
 high cellularity, high MIB-1 labeling index, and focal vascular proliferation, it was difficult to distinguish this lesion
 from HPC. However, the tumor was finally diagnosed as SFT on the basis of the stron...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517180</comments>
            <pubDate>Wed, 28 Apr 2010 08:29:56 +0100</pubDate>
            <guid isPermaLink="false">3517180</guid>        </item>
        <item>
            <title>A case of unclassified, radiosensitive, malignant neuroepithelial tumor in the temporal lobe of a child</title>
            <link>http://www.medworm.com/index.php?rid=3517179&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fagl288164l11258h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A case of unclassified, pediatric cerebral neuroepithelial tumor in a 10-year-old girl that showed remarkable radiosensitivity
 is reported. MRI revealed a brain tumor of mixed intensity with heterogeneous enhancement in the medial temporal lobe, extending
 to the basal ganglia. The tumor was partially removed. On pathology, the main part of the tumor showed immature features:
 the tumor cells had a chromatin-rich large nucleus and less cytoplasm, and mitoses and fragmentation of the nuclei were frequent.
 On immunohistochemistry, the tumor cells were negative for glial fibrillary acidic protein (GFAP) and synaptophysin and positive
 for Olig2. The maximum MIB-1 index was 70%. The part invading into the surrounding brain showed similarities in form to a
 highly anaplast...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3517179</comments>
            <pubDate>Wed, 28 Apr 2010 08:29:56 +0100</pubDate>
            <guid isPermaLink="false">3517179</guid>        </item>
        <item>
            <title>Mouse models of CNS embryonal tumors</title>
            <link>http://www.medworm.com/index.php?rid=2936707&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Feu7623510276742l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Central nervous system (CNS) embryonal tumors are devastating cancers in children, consisting of medulloblastomas, CNS primitive
 neuroectodermal tumors, and atypical teratoid/rhabdoid tumors. One of the reasons that CNS embryonal tumors remain difficult
 to treat is their rarity, which makes conducting clinical trials for these tumors difficult. Recent advances of molecular
 biology have led us to identify molecular and genetic causality of brain tumors. Based on the genetic alterations found in
 humans, multiple models of human CNS embryonal tumors have been generated in genetically engineered mice. These mouse models
 are valuable tools for understanding brain tumor biology and discovering novel therapeutic targets and drugs. In this article,
 we review molecular and...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936707</comments>
            <pubDate>Mon, 26 Oct 2009 05:56:39 +0100</pubDate>
            <guid isPermaLink="false">2936707</guid>        </item>
        <item>
            <title>Tanycytic ependymoma of the filum terminale with pleomorphic giant cells</title>
            <link>http://www.medworm.com/index.php?rid=2936709&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5pw7556q80554460%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A tanycytic ependymoma measuring 1.5 cm in maximal dimension, which involved the filum terminale and conus medullaris of a
 55-year-old woman, is reported. The tumor consisted of a compact fascicular proliferation of spindle cells having long bipolar
 cytoplasmic processes, and immunohistochemical and ultrastructural studies demonstrated the ependymal features of neoplastic
 cells. The most prominent finding was an appearance of many atypical and pleomorphic, often monstrous, giant cells, which
 was not associated with an increase in proliferative activity. Remarkable nuclear atypism and pleomorphism with formation
 of giant cells have not been documented previously in tanycytic ependymoma. These nuclear changes are considered essentially
 degenerative in nature and pro...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936709</comments>
            <pubDate>Mon, 26 Oct 2009 05:56:38 +0100</pubDate>
            <guid isPermaLink="false">2936709</guid>        </item>
        <item>
            <title>Primary Ewing’s sarcoma of the orbit: case report</title>
            <link>http://www.medworm.com/index.php?rid=2936708&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm3vq245867r112r7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 22-year-old man presented with tenderness and swelling of the left lateral part of the orbit. Computed tomography revealed
 a left intraorbital mass measuring 3 cm × 3 cm involving the left lateral wall of the orbit and the greater wing of the left
 sphenoid bone. Magnetic resonance imaging revealed that the intraorbital mass was extraneuroaxial. During surgery, the tumor
 was seen to arise from the lateral wall of the orbit and infiltrate into the left temporal muscle. Following the surgery,
 the patient was administered radiation therapy for the whole cranium and chemotherapy for the residual tumors. However, the
 tumor recurred, and the patient died about 2 years following the first surgery because the tumor had metastasized to the lung.
 On light microscopy, the ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936708</comments>
            <pubDate>Mon, 26 Oct 2009 05:56:38 +0100</pubDate>
            <guid isPermaLink="false">2936708</guid>        </item>
        <item>
            <title>Clinicopathological features from long-term observation of a papillary tumor of the pineal region (PTPR): a case report</title>
            <link>http://www.medworm.com/index.php?rid=2936710&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl9644t8260221hk4%2F</link>
            <description>We present a case of a 17-year-old man who developed a 3-cm pineal tumor that was incompletely
 excised following two operations. The pathological findings presented were extensive epithelial papillary structures surrounding
 vessels mimicking “perivascular pseudo-rosettes,” leading to a diagnosis of “papillary ependymoma.” Subsequently, the residual
 tumor recurred on three separate occasions. Immunohistochemical studies showed the tumor was positive for cytokeratin 18 (CK
 18), microtubule-associated protein (MAP 2), neuron-specific enolase (NSE), neuronal nuclei (NeuN), and transthyretin, consistent
 with mature neuronal differentiation. Given these findings, the diagnosis of PTPR was made. The patient’s survival time of
 218 months is the longest reported to date for this tum...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936710</comments>
            <pubDate>Mon, 26 Oct 2009 05:56:37 +0100</pubDate>
            <guid isPermaLink="false">2936710</guid>        </item>
        <item>
            <title>Sensitivity and usefulness of anti-phosphohistone-H3 antibody immunostaining for counting mitotic figures in meningioma cases</title>
            <link>http://www.medworm.com/index.php?rid=2936712&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkp4u064p1wn18041%2F</link>
            <description>In this study,
 we attempted PHH3 immunostaining for our meningioma cases and verified not only the sensitivity of PHH3 immunostaining but
 also that of its usefulness in grading meningiomas. Forty-five initial histologically confirmed meningiomas (37 benign, 7
 atypical, and 1 anaplastic) were reviewed according to current WHO criteria based on counting MF on HE-stained slides. PHH3-immunostained
 MF were counted in the same way, and the MIB-1 labeling index (LI) was calculated for each sample. PHH3-labeled MF were easily
 identified and permitted rapid recognition of the areas of highest mitotic activity. As a result, significant increase of
 PHH3 mitotic index (PHH3-MI) in comparison with HE mitotic index (HE-MI) and strong correlations with HE-MI to PHH3-MI as
 well as PHH3-MI to MIB-1...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936712</comments>
            <pubDate>Mon, 26 Oct 2009 05:56:36 +0100</pubDate>
            <guid isPermaLink="false">2936712</guid>        </item>
        <item>
            <title>Recurrence and regrowth of benign meningiomas</title>
            <link>http://www.medworm.com/index.php?rid=2936711&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu635166254mq6628%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The World Health Organization (WHO) grading system for meningioma is helpful for predicting aggressive subtypes. However,
 even benign meningiomas sometimes show relatively rapid growth and may recur after total removal. We attempted to find histopathological
 features that would be valuable for predicting recurrence or regrowth of WHO grade I meningiomas. We investigated 135 benign
 meningiomas, of which 120 were totally removed (Simpson’s grade I–III). The median follow-up period was 9.7 years (1–21 years).
 The recurrence rate in the patients with total removal was 7.5% at 10 years and 9.3% at 20 years. The univariate analysis
 revealed that MIB-1 index (≥2%), existence of mitosis, absence of calcification, and paucity of fibrosis significantly correlated
 wi...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936711</comments>
            <pubDate>Mon, 26 Oct 2009 05:56:36 +0100</pubDate>
            <guid isPermaLink="false">2936711</guid>        </item>
        <item>
            <title>Collision tumor of anaplastic oligodendroglioma and gangliocytoma: a case report</title>
            <link>http://www.medworm.com/index.php?rid=2936715&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj555r1630173u53l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 53-year-old woman presented with a rare case of coexistence of anaplastic oligodendroglioma with gangliocytoma manifesting
 as progressive disturbance of consciousness and left hemiparesis. Magnetic resonance imaging with gadolinium demonstrated
 the mass lesion consisted of a strongly enhanced area around the middle cerebral artery and less enhanced areas in the right
 temporal lobe, insula, and basal ganglia. She underwent subtotal resection of the tumor, resulting in improvement of her symptoms.
 Macroscopic and histological examination showed the tumor consisted of two distinct components, grayish soft tissue and yellowish
 hard tissue. The former consisted of cells with equal-sized round-to-oval hyperchromatic nuclei and perinuclear halo with
 microvascular proli...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936715</comments>
            <pubDate>Mon, 26 Oct 2009 05:56:34 +0100</pubDate>
            <guid isPermaLink="false">2936715</guid>        </item>
        <item>
            <title>Radiopathological characteristics of cerebellar malignant glioma in adults</title>
            <link>http://www.medworm.com/index.php?rid=2936714&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj6540kw1t37p8425%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Our aim was to extract the radiopathological features of cerebellar malignant glioma in adults from the four cases we encountered.
 All four cases (two men and two women, aged 52–80 years; mean age, 67 years) had a floating sensation or vertigo at the onset
 of their disease. Initially, these patients were given a diagnosis of cerebellar infarction or cavernous angioma, or had faint
 abnormalities in the cerebellum that were overlooked. These patients were followed up for 2–14 months (mean, 6 months), and
 the tumor was detected when their clinical symptoms deteriorated. The tumor was located in the hemisphere in one patient and
 in the vermis in three patients. MRI revealed ring-like enhancement in two patients and nodular enhancement in two patients.
 All patients...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936714</comments>
            <pubDate>Mon, 26 Oct 2009 05:56:34 +0100</pubDate>
            <guid isPermaLink="false">2936714</guid>        </item>
        <item>
            <title>Successful treatment of neoadjuvant therapy for papillary tumor of the pineal region</title>
            <link>http://www.medworm.com/index.php?rid=2936713&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjj71u268q214pn42%2F</link>
            <description>We report a boy who in 1994, at the age of 11, presented with headache and vomiting. The fi nal diagnosis was papillary tumor
 of the pineal region (PTPR). Magnetic resonance imaging (MRI) revealed a heterogeneous mass. Hydrocephalus was addressed by
 immediate ventricle drainage; subsequently, we attempted tumor removal. As the intraoperative diagnosis of the hemorrhagic
 tumor was primitive neuroectodermal tumor (PNET), we did not proceed to total removal. After the delivery of radiotherapy
 (50.4 Gy) and one course of Nimustine hydrochloride (ACNU) chemotherapy, the residual tumor was completely resected. The diagnosis
 at that time (1994) was papillary pineocytoma. He was followed on an outpatient basis for 15 years and remained free of recurrence.
 This type of tumor was later propose...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936713</comments>
            <pubDate>Mon, 26 Oct 2009 05:56:34 +0100</pubDate>
            <guid isPermaLink="false">2936713</guid>        </item>
        <item>
            <title>A rare astrocytic tumor with rhabdoid features</title>
            <link>http://www.medworm.com/index.php?rid=2384444&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu5jk20521051033q%2F</link>
            <description>We report an extremely rare tumor presenting with rhabdoid features in the left temporoparietal lobe near the trigone in an
 18-year-old Japanese man. This tumor mainly consisted of medium to large round cells that proliferated diffusely and incoherently
 with a scant extracellular matrix. These tumor cells had an eccentric nucleus and an eosinophilic cytoplasm containing inclusion
 bodies and bundles of intermediate filaments. The nuclei of these cells were vesicular with prominent nucleoli. This tumor
 had an area appearing to be diffuse astrocytoma peripherally and lacked a primitive neuroectodermal tumor component, a mesenchymal
 component, and epithelial differentiation. INI expression, which is not observed in atypical teratoid/ rhabdoid tumor (AT/RT),
 was found in this tumor. From ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2384444</comments>
            <pubDate>Fri, 01 May 2009 06:32:05 +0100</pubDate>
            <guid isPermaLink="false">2384444</guid>        </item>
        <item>
            <title>A case of a heavily pigmented orbital melanocytoma</title>
            <link>http://www.medworm.com/index.php?rid=2384447&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj6703g3662688176%2F</link>
            <description>We present an extremely rare case of an orbital melanocytoma that occurred in a 51-year-old man. The patient suffered from
 diplopia and mild exophthalmos of the right eye for 2 months. Brain magnetic resonance imaging showed a well-demarcated round
 mass 3.5 cm in diameter in the right orbit. We performed total resection of this tumor. Histological findings revealed a proliferation
 of large polygonal cells with fine pigment granules in the cytoplasm and prominent nucleoli. Although these tumor cells revealed
 immunohistochemical reactivity in HMB-1, there was no S-100 or Melan A antibody reactivity. Also, there were no malignant
 findings of nuclear polymorphism, mitoses, or necrosis. The brown pigments were confirmed to be melanin by bleaching and the
 Fontana-Masson silver stain method...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2384447</comments>
            <pubDate>Fri, 01 May 2009 06:32:04 +0100</pubDate>
            <guid isPermaLink="false">2384447</guid>        </item>
        <item>
            <title>Ultrastructural and immunohistochemical study of an adult case of chordoid meningioma</title>
            <link>http://www.medworm.com/index.php?rid=2384446&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3363558517585080%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 64-year-old male patient presented with generalized convulsions. Magnetic resonance imaging revealed a large meningeal tumor
 with some cysts in the right frontal region. Surgical resections were performed three times, and local radiation therapy was
 administered twice over a period of 8 years for the treatment of tumor recurrences. The tumor tended to recur in spite of
 the surgical and radiation therapies. The tumor was diagnosed as a chordoid meningioma, and the second surgical specimen showed
 increasing nuclear atypia and mitoses in tumor cells. An immunohistochemical study revealed the tumor cells were positive
 for vimentin, S-100 protein, and cytokeratin AE1/AE3. An electron microscopic study revealed intracytoplasmic vacuolar spaces,
 loosely connected inter...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2384446</comments>
            <pubDate>Fri, 01 May 2009 06:32:04 +0100</pubDate>
            <guid isPermaLink="false">2384446</guid>        </item>
        <item>
            <title>Hemorrhagic onset of pilocytic astrocytoma and pilomyxoid astrocytoma</title>
            <link>http://www.medworm.com/index.php?rid=2384445&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkx278r374457h783%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The incidence of hemorrhagic onset in pilocytic astrocytoma and pilomyxoid astrocytoma, and the clinical and histological
 characteristics, were compared to other types of neuroepithelial tumors or nonhemorrhagic pilocytic astrocytoma by retrospective
 review of 445 consecutive neuroepithelial tumors treated at our institute. Hemorrhagic onset was observed in 4 of 35 (11.4%)
 patients with pilocytic astrocytoma and pilomyxoid astrocytoma, with higher incidence than in glioblastoma (3.9%), anaplastic
 oligodendroglioma (7.7%), and anaplastic ependymoma (7.1%). The hemorrhagic onset occurred in 2 patients with sporadic pilocytic
 astrocytoma, 1 with pilocytic astrocytoma associated with neurofibromatosis type 1, and 1 with pilomyxoid astrocytoma. There
 was no correlation...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2384445</comments>
            <pubDate>Fri, 01 May 2009 06:32:04 +0100</pubDate>
            <guid isPermaLink="false">2384445</guid>        </item>
        <item>
            <title>Pleomorphic xanthoastrocytoma as a component of a temporal lobe cystic ganglioglioma: a case report</title>
            <link>http://www.medworm.com/index.php?rid=2384449&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhl44q1264ng35876%2F</link>
            <description>We report a case of pleomorphic xanthoastrocytoma (PXA) as a component of a ganglioglioma in a 13-year-old Japanese boy. Magnetic
 resonance imaging showed a large cystic lesion with an enhanced mural nodule of the left temporal lobe. Microscopic examination
 of the tumor showed that it was composed of two distinct neoplastic components: dysplastic ganglion cells and a PXA. There
 were gradual transitions between the two neoplastic components, and the PXA constituted the gliomatous component of the ganglioglioma.
 The PXA component showed spindle-shaped and pleomorphic large cells with lipidized cytoplasm. The tumor cells were surrounded
 by numerous reticulin fibers. Immunohistochemically, the ganglion cells were negative for glial fibrillary acidic protein
 (GFAP), but showed positive st...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2384449</comments>
            <pubDate>Fri, 01 May 2009 06:32:03 +0100</pubDate>
            <guid isPermaLink="false">2384449</guid>        </item>
        <item>
            <title>A case of an anaplastic ependymoma with gliosarcomatous components</title>
            <link>http://www.medworm.com/index.php?rid=2384448&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr3w0wl4j27563868%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 29-year-old woman presented with a severe headache. Computed tomography revealed a large cystic lesion with a mural nodule-like
 mass homogeneously enhanced with contrast medium in the right cerebellum. The tumor was removed, and pathological studies
 revealed a cerebellar astrocytoma corresponding to World Health Organization grade II. When she was 35 years old, or 6 years
 after the surgery, magnetic resonance imaging revealed a recurrence of the tumor in the right cerebellum, and subtotal removal
 of the recurrent tumor was performed. Pathological studies revealed a mixed glioblastoma multiforme and anaplastic ependymoma.
 Chemotherapy (Paraplatin and VePeside-S) and focal radiation therapy at 60 Gy were administered following surgery. Thereafter,
 at 39 years of a...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2384448</comments>
            <pubDate>Fri, 01 May 2009 06:32:03 +0100</pubDate>
            <guid isPermaLink="false">2384448</guid>        </item>
        <item>
            <title>Tanycytic ependymoma of the spinal cord with anaplastic cytological features</title>
            <link>http://www.medworm.com/index.php?rid=2384450&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9755n4t47385w85h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In a 43-year-old man, an intramedullary spinal cord tumor spreading from the level of the T2 to T5 vertebrae was subtotally
 resected. The tumor predominantly consisted of a fascicular proliferation of spindle cells having bland nuclei and bipolar,
 long cytoplasmic processes, and a few perivascular pseudo-rosettes were found. Although there were no true ependymal rosettes,
 intracytoplasmic dot-like immunoreactivity for epithelial membrane antigen (EMA) was found in a few cells. In some areas,
 a dense and diffuse proliferation of anaplastic, short-spindled cells having hyperchromatic nuclei and scant cytoplasm was
 noted, and the Ki-67 labeling index was remarkably higher (18.2%) in these areas. Neither microvascular proliferation nor
 necrosis was observed. In the bo...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2384450</comments>
            <pubDate>Fri, 01 May 2009 06:32:02 +0100</pubDate>
            <guid isPermaLink="false">2384450</guid>        </item>
        <item>
            <title>Immunohistochemical analysis of adhesion molecules and matrix metalloproteinases in malignant CNS lymphomas: a study comparing primary CNS malignant and CNS intravascular lymphomas</title>
            <link>http://www.medworm.com/index.php?rid=1944711&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F422gm3441522354l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two distinct forms of malignant lymphomas can invade the central nervous system (CNS). Although primary CNS malignant lymphomas
 (PCNSMLs) invade the brain parenchyma, intravascular lymphomas (IVLs) form tumor cell aggregates in the vasculature and produce
 stroke-like symptoms and cognitive impairment. Although the tumor cells are mostly of B-cell origin in both types of lymphoma,
 their biological behavior is different, and the detailed mechanism(s) underlying this difference are not well understood.
 We studied the expression level of the adhesion molecules intercellular adhesion molecule-1 (ICAM-1) and integrin-β1 in tumor
 tissue samples from patients with primary CNS lymphoma (n = 8) and intravascular lymphoma (n = 2) using immunohistochemical analysis. We also a...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944711</comments>
            <pubDate>Thu, 06 Nov 2008 00:31:35 +0100</pubDate>
            <guid isPermaLink="false">1944711</guid>        </item>
        <item>
            <title>Papillary tumor of the pineal region: a case report</title>
            <link>http://www.medworm.com/index.php?rid=1944710&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc28wk2062x3607v2%2F</link>
            <description>We report a case of papillary tumor of the pineal region (PTPR) and describe the morphological, immunohistochemical, and neuroimaging
 findings. A 43-year-old man presented with signs of increased intracranial pressure and upward gaze palsy. Magnetic resonance
 (MR) imaging demonstrated a heterogeneously enhanced mass in the pineal region and obstructive hydrocephalus. Proton MR spectroscopy
 revealed increased choline and decreased N-acetyl aspartate peaks with a slightly increased lactate peak. Minimum apparent diffusion coefficient value was 0.60 × 10−3 mm2/s. Positron emission tomography showed significantly increased [18F]fluorodeoxyglucose uptake at the site of the lesion. He underwent total resection of the pineal region mass, resulting in
 resolution of the symptoms. The tumor c...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944710</comments>
            <pubDate>Thu, 06 Nov 2008 00:31:35 +0100</pubDate>
            <guid isPermaLink="false">1944710</guid>        </item>
        <item>
            <title>Pathological review of late cerebral radionecrosis</title>
            <link>http://www.medworm.com/index.php?rid=1944709&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv32t159u75988v80%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Late cerebral radionecrosis may be considered to be a specific chronic inflammatory response, although it is unknown whether
 the initial damage by brain irradiation is to an endothelial cell or a glial cell. I discuss the pathological specificity
 of late cerebral radionecrosis by studying the published literature and a case that I experienced. In late cerebral radionecrosis,
 there are typical coagulation necrosis areas containing fibrinoid necrosis with occlusion of the lumina and poorly active
 inflammatory areas with many inflammatory ghost cells, focal perivascular lymphocytes, hyalinized vessels, and telangiectatic
 vascularization near and in the necrotic tissue, and more active inflammatory areas formed as a partial rim of the reactive
 zone by perivascular lym...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944709</comments>
            <pubDate>Thu, 06 Nov 2008 00:31:35 +0100</pubDate>
            <guid isPermaLink="false">1944709</guid>        </item>
        <item>
            <title>An immunohistochemical and electron microscopic study of atypical teratoid/rhabdoid tumor</title>
            <link>http://www.medworm.com/index.php?rid=1944714&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3824jrh347q32q5w%2F</link>
            <description>We report two infant cases with atypical teratoid/rhabdoid tumor (AT/RT) located in the cerebellar vermis and spinal cord.
 MRI showed the tumors were isointense on T1-weighted images and mixed intensity of isointense and slight high intensity on T2-weighted images. Postcontrast MRI demonstrated clear margin of tumor and heterogeneous strong enhancement. It was difficult
 to differentiate the tumor from medulloblastoma by hematoxylin and eosin staining. However, immunohistochemical staining showed
 that these tumor cells react positively for cytokeratin, smooth muscle actin (SMA), and epithelial membrane antigen (EMA)
 and helped us with the differentiation. Electron microscopic study has confirmed the presence of mesenchymal components, such
 as filaments and desmosome junctions in the rh...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944714</comments>
            <pubDate>Thu, 06 Nov 2008 00:31:34 +0100</pubDate>
            <guid isPermaLink="false">1944714</guid>        </item>
        <item>
            <title>Lymphocytic infundibulo-neurohypophysitis and infundibulo-panhypophysitis regarded as lymphocytic hypophysitis variant</title>
            <link>http://www.medworm.com/index.php?rid=1944713&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb38361857762h301%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Lymphocytic infundibulo-neurohypophysitis (LINH) was first reported by Saito et al. and Imura et al. as a cause of idiopathic
 central diabetes insipidus. Magnetic resonance (MR) imaging with a contrast medium demonstrates thickening of the pituitary
 stalk, enlargement of the neurohypophysis, or both with homogeneous enhancement. Histological examination reveals a posterior
 pituitary that is heavily infiltrated by lymphocytes with occasional plasma cells and other inflammatory cells. In early reports
 of the disorder, the lesion seemed to be limited to the neurohypophysis, but the present review showed cases with a combination
 of hypopituitarism and diabetes insipidus. Some of them showed partial hypopituitarism. The so-called lymphocytic infundibulo-panhypophysitis
...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944713</comments>
            <pubDate>Thu, 06 Nov 2008 00:31:34 +0100</pubDate>
            <guid isPermaLink="false">1944713</guid>        </item>
        <item>
            <title>Brain tumor stem cells as research and treatment targets</title>
            <link>http://www.medworm.com/index.php?rid=1944712&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk292x8v457g04707%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioblastoma multiforme (GBM) is one of the most malignant forms of human cancer. Despite intensive treatment, the mean survival
 of GBM patients remains about 1 year. Recent cancer studies revealed that cancer tissues are pathologically heterogeneous
 and only a small population of cells has the specific ability to reinitiate cancer. This small cell population is called cancer
 stem cells (CSCs); in brain tumors these are known as brain tumor stem cells (BTSCs). The identification of BTSCs yielded
 new insights into chemo-and radioresistance, by which BTSCs can survive selectively and initiate recurrence. Research focused
 on BTSCs as treatment targets may contribute to the discovery of new therapeutic strategies.
 
	Content Type Journal ArticleCategory Review ArticleD...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944712</comments>
            <pubDate>Thu, 06 Nov 2008 00:31:34 +0100</pubDate>
            <guid isPermaLink="false">1944712</guid>        </item>
        <item>
            <title>Expansile neurenteric cyst arising in the frontal lobe associated with status epilepticus: report of a case and discussion of epileptogenesis</title>
            <link>http://www.medworm.com/index.php?rid=1944716&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj766375785v68883%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The case of a 32-year-old Japanese man with an expansile supratentorial neurenteric cyst is described. The initial MRI revealed
 a left frontal extraaxial mass lesion 20 mm in diameter that showed marked expansion to 32 mm and change in its signal intensity
 13 months later. Fifteen months after his visit, the patient fell into status epilepticus and underwent surgery. The cyst
 wall was excised, and the cyst content was totally removed. The cytology of the cystic content and pathological findings of
 the cyst wall were compatible with the diagnosis of neurenteric cyst. Our literature search revealed that in 86% of the patients
 with this lesion, the lesion was involved in the occurrence of epilepsy during the perioperative period. When a neurenteric
 cyst is diagnosed,...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944716</comments>
            <pubDate>Thu, 06 Nov 2008 00:31:33 +0100</pubDate>
            <guid isPermaLink="false">1944716</guid>        </item>
        <item>
            <title>Chordoid meningioma arising in the pineal region: a case report</title>
            <link>http://www.medworm.com/index.php?rid=1944715&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft0600p240k8534rp%2F</link>
            <description>We report a rare case of chordoid meningioma arising in the pineal region, which presented in a 22-year-old woman. Her only
 complaint was headache, and neurological examination revealed no deficits. She had suffered from prolonged fever a few weeks
 earlier, and her hematological findings included hypochromic microcytic anemia and a high serum level of C-reactive protein
 (CRP). Cranial magnetic resonance (MR) images demonstrated a 25 × 30 mm mass in the pineal region, which showed iso-to low
 intensity on T1-weighted images (T1WI), high to low intensity on T2-weighted images (T2WI), and homogeneous enhancement with gadolinium-diethylenetriaminepentaacetic acid (Gd-DTPA). We performed
 subtotal removal of the tumor with an occipital transtentorial approach (OTA), and all her preoperative...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944715</comments>
            <pubDate>Thu, 06 Nov 2008 00:31:33 +0100</pubDate>
            <guid isPermaLink="false">1944715</guid>        </item>
        <item>
            <title>A case of lymphomatoid granulomatosis followed for 14 months on the basis of clinical and histological findings</title>
            <link>http://www.medworm.com/index.php?rid=1380385&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flr215g6383t2n6r5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Lymphomatoid granulomatosis (LYG) is a systemic granulomatous disease characterized by B-cell proliferation of uncertain malignant
 potential. It most frequently affects the lungs but also occasionally affects the central nervous system. Its pathophysiology
 is unclear in numerous respects, thus making it difficult to diagnose and treat. We recently encountered a case of LYG that
 was followed clinically and histologically for 14 months. A 55-year-old man was hospitalized with multiple brain tumors for
 which the final diagnosis was not made until the second surgery, 14 months after the first intervention. Following the diagnosis,
 he was treated with steroid pulse therapy. At present, 3.5 years after the onset of LYG, the patient is in good condition
 with no signs of ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1380385</comments>
            <pubDate>Wed, 16 Apr 2008 15:01:41 +0100</pubDate>
            <guid isPermaLink="false">1380385</guid>        </item>
        <item>
            <title>Ultrastructural study of neuronal and related tumors in the ventricles</title>
            <link>http://www.medworm.com/index.php?rid=1380386&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc626x7242l052171%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intraventricular tumors may arise from a variety of cells in the region. There are some difficulties in diagnosing these tumors
 because of their histologically similar appearance. We analyzed intraventricular tumors, including central neurocytoma, oligodendroglioma,
 cerebral neuroblastoma, and cerebellar neuroblastoma, the neuronal characters of which were established based on their ultrastructural
 findings, except for oligodendroglioma. Central neurocytoma and cerebellar neuroblastoma showed synaptic formation, and cerebral
 neuroblastoma possessed immature neurites. Oligodendroglioma showed similar structures to that of a normal oligodendrocyte.
 Furthermore, we review the literature and evaluate the usefulness of analyzing ultrastructures.
 
	Content Type Journal ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1380386</comments>
            <pubDate>Wed, 16 Apr 2008 15:01:39 +0100</pubDate>
            <guid isPermaLink="false">1380386</guid>        </item>
        <item>
            <title>Medulloblastoma demonstrating multipotent differentiation: case report</title>
            <link>http://www.medworm.com/index.php?rid=1380390&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb2746314knr25672%2F</link>
            <description>We report a 6-year-old boy who presented with a medulloblastoma demonstrating classic, myoblastic, neuronal, glial, and melanotic
 differentiation and manifesting as severe morning headache. Magnetic resonance imaging revealed a mass lesion with cystic
 components in the cerebellar vermis. He underwent suboccipital craniotomy and total resection of the tumor. The specimen consisted
 of three morphologically distinct components. The first component consisted of densely packed cells with round-to-oval highly
 hyperchromatic nuclei surrounded by scanty cytoplasm. Immunohistochemical staining revealed diffuse expression of neurofilament
 protein and focal expression of desmin and myoglobin. The second component consisted of long spindle-shaped cells with elongated
 nuclei and eosinophilic cyto...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1380390</comments>
            <pubDate>Wed, 16 Apr 2008 15:01:36 +0100</pubDate>
            <guid isPermaLink="false">1380390</guid>        </item>
        <item>
            <title>Evaluation of sensitivity and specificity of doublecortin immunostatining for the detection of infiltrating glioma cells</title>
            <link>http://www.medworm.com/index.php?rid=1380389&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkl0k0571j5655t46%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Diffuse gliomas are highly infiltrative intracranial tumors, but there are few useful markers for detecting infiltrating glioma
 cells in the surrounding brain tissue. Doublecortin (DCX) is a microtubule-associated protein (MAP) that plays a crucial role
 in neuroblast migration. It was recently demonstrated that DCX is preferentially expressed in invasive gliomas. However, the
 sensitivity and specificity of DCX as a marker for infiltrating glioma cells have not been fully evaluated. We immunohistochemically
 analyzed the expression pattern of DCX in human gliomas and compared it with that of MAP-2e, another marker for infiltrating
 glioma cells. We found that DCX was expressed specifically in infiltrating gliomas, but not in reactive, existing glia. Not
 all our cases...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1380389</comments>
            <pubDate>Wed, 16 Apr 2008 15:01:36 +0100</pubDate>
            <guid isPermaLink="false">1380389</guid>        </item>
        <item>
            <title>Consecutive histological changes in an astroblastoma that disseminated to the spinal cord after repeated intracranial recurrences: a case report</title>
            <link>http://www.medworm.com/index.php?rid=1380388&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu312331n42705302%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 17-year-old male patient underwent surgery five times (four consecutive intracranial tumor removal surgeries and a final
 spinal tumor removal surgery). After the third surgery, this case was reported as a low-grade astroblastoma that is characterized
 by perivascular pseudorosettes consisting of elongated tumor cells arranged around the blood vessels. However, the fourth
 and fifth surgical specimens demonstrated very interesting histological changes in the astroblastoma. Through the course of
 relapses, the constituent cells of the astroblastic perivascular rosettes became smaller and rounder, and a multilayered cell
 arrangement was observed. The nucleus-to-cytoplasm ratio increased, and the compact intervascular cells ultimately lost glial
 fibrillary acidic prote...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1380388</comments>
            <pubDate>Wed, 16 Apr 2008 15:01:36 +0100</pubDate>
            <guid isPermaLink="false">1380388</guid>        </item>
        <item>
            <title>Frequent and variable abnormalities in p14 tumor suppressor gene in glioma cell lines</title>
            <link>http://www.medworm.com/index.php?rid=1380387&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F441037h02609v012%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ten glioma cell lines were examined for abnormalities of exon 1β of the p14 gene and then for abnormalities of the entire
 p14 gene with the use of previous findings of other exons. Abnormalities of exon 1β and the entire p14 gene were detected
 in eight of ten cases: homozygous deletion of the entire gene in six cases, hemizygous deletion of exon 1β with homozygous
 deletion of downstream exons in one case, and hemizygous deletion of the entire coding region with a missense mutation (A97V)
 at the C-terminal nucleolar localization domain in one case. The remaining two cases revealed tno such abnormalities. p14
 gene expression was observed in the latter two cases and one case with A97V mutation in the hemizygously deleted coding region,
 but not in the others, inclu...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1380387</comments>
            <pubDate>Wed, 16 Apr 2008 15:01:36 +0100</pubDate>
            <guid isPermaLink="false">1380387</guid>        </item>
        <item>
            <title>A case of cerebral ganglioneuronal tumor in the parietal lobe of an adult</title>
            <link>http://www.medworm.com/index.php?rid=1380391&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F352407612234n231%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Central nervous system (CNS) neuroblastoma/ganglioneuroblastoma is one of the embryonal tumors with neuronal differentiation
 found in young adults, but it is most common in children, especially in those below the age of 5 years, whereas extraventricular
 neurocytoma, a rare neuroepithelial tumor with neuronal differentiation, mostly affects young adults. Here we present a rare
 case of cerebral ganglioneuronal tumor that occurred in a 32-year-old woman. The patient suffered from tonic convulsion, and
 computed tomography demonstrated a well-demarcated, round tumor 3.3 cm in size with marked calcification in the right parietal
 lobe. Histological analysis revealed diffuse infiltration of small, round cells with scattered large ganglion-like cells.
 Immunohistochemically...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1380391</comments>
            <pubDate>Wed, 16 Apr 2008 15:01:34 +0100</pubDate>
            <guid isPermaLink="false">1380391</guid>        </item>
        <item>
            <title>An infant case of intracranial peripheral-type primitive neuroectodermal tumor with long-term survival</title>
            <link>http://www.medworm.com/index.php?rid=1047347&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq7201q275h4w7366%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp; Supratentorial primitive neuroectodermal tumors (S-PNET) that develop in children have recently been classified into two
 types: central-type PNET (C-PNET), which has been reported over the years, and peripheral-type PNET (P-PNET), which develops
 intracranially and was referred to as Ewing's sarcoma in the past. P-PNET is fundamentally a malignant tumor, but the patient
 reported here represents a case of long-term survival from onset without recurrence. At the age of 21 months, a male infant
 developed a cranial bone deformity and symptoms of high intracranial pressure. A CT scan revealed a cystic tumor attaching
 to the falx, and cyst drainage operation was immediately performed. The intracranial tumor was then resected. The tumor was
 an intradural extramedullary t...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1047347</comments>
            <pubDate>Wed, 21 Nov 2007 16:42:17 +0100</pubDate>
            <guid isPermaLink="false">1047347</guid>        </item>
        <item>
            <title>Expression of aquaporine-4 in central nervous system tumors</title>
            <link>http://www.medworm.com/index.php?rid=1047345&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F922837x940505585%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cerebral edema is associated with common brain tumors. Aquaporine-4 (AQP4) is a member of the water channel protein family,
 which is thought to be a major factor regulating cerebral edema. To elucidate the characterization of the expression of AQP4
 and the relationship of the expression of VEGF, we investigated the expression of AQP4 in tumors of the central nervous system
 immunohistochemically. Brain tumors and nontumorous cerebral tissue for control were evaluated by immunohistochemical staining
 using anti-AQP4, VEGF, CD34, and MIB-1. In tumor cells, only glial tumor cells showed a positive reaction for AQP4. The reactivities
 for immunostaining increased according to WHO grades. Reactive glial cells in edematous tissue also showed positive reactions.
 Although en...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1047345</comments>
            <pubDate>Wed, 21 Nov 2007 16:42:17 +0100</pubDate>
            <guid isPermaLink="false">1047345</guid>        </item>
        <item>
            <title>A rare case of malignant glioma suspected to have arisen from a cavernous sinus</title>
            <link>http://www.medworm.com/index.php?rid=1047344&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1581517162062315%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 55-year-old woman presented with a right trigeminal dysfunction (dysesthesia) initially, followed by right oculomotor and
 abducens paresis lasting 1 month. Neuroimaging studies showed an enhanced mass in the right cavernous sinus extending to the
 trigeminal ganglion. The extraparenchymal tumor located around the right trigeminal ganglion was totally removed, except for
 an intracavernous lesion, by the orbitozygomatic approach. The solid tumor was completely separated from the brainstem and
 seemed to be a trigeminal schwannoma arising from the trigeminal ganglion or cavernous sinus at surgery. A histological examination,
 however, found a typical malignant glioma that consisted primarily of astrocytic tumor cells. Immunohistochemical staining
 showed the tumor cell...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1047344</comments>
            <pubDate>Wed, 21 Nov 2007 16:42:17 +0100</pubDate>
            <guid isPermaLink="false">1047344</guid>        </item>
        <item>
            <title>Malignant transformation of oligoastrocytoma: a case report</title>
            <link>http://www.medworm.com/index.php?rid=1047342&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh4508258x3r5764j%2F</link>
            <description>We report a case of oligoastrocytoma resembling dysembryoplastic neuroepithelial tumor (DNT) with malignant transformation.
 A 35-year-old woman presented with headache and generalized convulsion in May 2003. Magnetic resonance imaging (MRI) revealed
 an extensive left temporal lobe tumor. She underwent partial resection of the tumor under awake surgery, while preserving
 her language function. The surgical specimen showed that the majority of the tumor was composed of a glioneuronal element.
 However, there was also an abundant oligoastrocytoma component. Therefore, our first pathological diagnosis was oligoastrocytoma
 and DNT. She then underwent radiation therapy. The tumor recurred at the left temporal lobe in June 2005. She then underwent
 open biopsy. The pathological diagnosis was a...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1047342</comments>
            <pubDate>Wed, 21 Nov 2007 16:42:17 +0100</pubDate>
            <guid isPermaLink="false">1047342</guid>        </item>
        <item>
            <title>Fluorescence-guided resection of metastatic brain tumors using a 5-aminolevulinic acid-induced protoporphyrin IX: pathological study</title>
            <link>http://www.medworm.com/index.php?rid=1047349&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0u73388167836wkx%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We performed a pathological study to identify the locus of production of protoporphyrin IX (PPIX) in human metastatic brain
 tumors. Patients with metastatic brain tumors (n = 11) received 1 g of 5-aminolevulinic acid (5-ALA) perorally 2 h before undergoing surgery. The target region was exposed
 to laser light with a peak wavelength of 405 � 1 nm and an output of 40 mW. Tissue samples from the tumor bulk and surrounding
 areas were examined by histological and fluorescence methods. Of the 11 tumors, 9 manifested PPIX fluorescence in the tumor
 bulk and peritumoral brain tissue. Our findings indicate that PPIX fluorescence can be observed in peritumoral edematous areas
 that are free of neoplastic cells, because PPIX produced by neoplastic cells leaks into the...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1047349</comments>
            <pubDate>Wed, 21 Nov 2007 16:42:16 +0100</pubDate>
            <guid isPermaLink="false">1047349</guid>        </item>
        <item>
            <title>Analysis of immunohistochemical expression of p53 and the proliferation marker Ki-67 antigen in skull base chordomas: relationships between their expression and prognosis</title>
            <link>http://www.medworm.com/index.php?rid=1047348&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy183283r5423u86x%2F</link>
            <description>We examined the expression of p53 and the MIB-1 labeling index (LI),
 assessed by Ki-67 expression, in 19 tumors (initial, n = 11; recurrent, n = 8) from 11 patients. The correlation among the MIB-1 LI, p53 expression, and the clinical outcome was analyzed. The mean
 MIB-1 LI and p53 expression at the initial surgery were 5.6 � 4.6% and 9.0 � 9.4%, respectively. At the time of recurrence,
 the mean MIB-1 LI and p53 expression were 10.2 � 7.4% and 16.5 � 12.0%. The correlation between the MIB-1 LI and p53 expression
 at the initial and recurrent surgeries was highly significant (r = 0.948; P &amp;lt; 0.0001). The change in p53 expression from the initial to the recurrent chordomas was significantly greater in patients
 who died of tumor-related causes than in the surviving patients. In ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1047348</comments>
            <pubDate>Wed, 21 Nov 2007 16:42:16 +0100</pubDate>
            <guid isPermaLink="false">1047348</guid>        </item>
        <item>
            <title>The usefulness and problem of intraoperative rapid diagnosis in surgical neuropathology</title>
            <link>http://www.medworm.com/index.php?rid=1047346&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8454774v88756738%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intraoperative rapid diagnosis has been a useful neurosurgery tool for maximal resection and minimal morbidity. However, only
 a few studies have been conducted regarding diagnostic accuracy and associated problems. The present study reviews our experience
 in treating patients and investigates the accuracy and problems associated with intraoperative rapid diagnosis in surgical
 neuropathology. There were 180 cases of intracranial lesions excluding pituitary lesions. The patients consisted of 89 males
 and 91 females, ranging from 5 months to 84 years, with a mean age of 46 years. Of the 180 cases, 152 cases received open
 surgery, 28 cases had stereotactic surgery including a biopsy and were histologically verified. The correlation between the
 intraoperative diagnosis...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1047346</comments>
            <pubDate>Wed, 21 Nov 2007 16:42:16 +0100</pubDate>
            <guid isPermaLink="false">1047346</guid>        </item>
        <item>
            <title>Hyperprolactinemia and immunohistochemical expression of intracellular prolactin and prolactin receptor in primary central nervous system tumors and their relationship with cellular replication</title>
            <link>http://www.medworm.com/index.php?rid=1047343&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg817031444k58228%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The role of prolactin (PRL) in the CNS remains uncertain. We evaluated the presence of hyperprolactinemia, intracellular prolactin
 (ICP), and prolactin receptor (PRL-R) in primary CNS tumors, and their relationship with cellular replication with a prospective
 cross-sectional study of 82 consecutive patients with primary CNS tumors admitted for neurosurgical resection between October
 2003 and September 2005. Patients submitted to a questionnaire, and venous blood samples were obtained for measurement of
 serum PRL and TSH. Immunohistochemical analyses were performed to evaluate the presence of ICP, PRL-R, and Ki-67. Serum PRL
 levels ranged from 2 to 70 ng/ml, and hyperprolactinemia was detected in 25 cases (30.5%). ICP was detected in 18 patients
 (21.9%), in whom ...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1047343</comments>
            <pubDate>Wed, 21 Nov 2007 16:42:16 +0100</pubDate>
            <guid isPermaLink="false">1047343</guid>        </item>
        <item>
            <title>Comparison of numerical change of epidermal growth factor receptor gene among pre- and postradiation glioma, and gliosis, and its clinical use</title>
            <link>http://www.medworm.com/index.php?rid=643665&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F58210958k8075001%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Surgery with following chemoradiotherapy is the mainstream glioma treatment. In the course of postradiation events, however,
 it is sometimes difficult for neurosurgeons, radiologists, and pathologists to discriminate tumor recurrence from radiation
 necrosis. The epidermal growth factor receptor (EGFR) gene, on chromosome 7, is known to gain in copy number frequently in high-grade gliomas. The authors applied the fluorescence
 in situ hybridization (FISH) method to observe the gene's numerical status in pre- and postradiation glioma samples to elucidate
 whether this technique is useful in the discrimination of glioma recurrence from radiation necrosis. When 15 postradiation
 glioma samples and 4 postradiation nonglioma samples were tested, all the recurrent glioma tis...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=643665</comments>
            <pubDate>Sat, 26 May 2007 14:36:14 +0100</pubDate>
            <guid isPermaLink="false">643665</guid>        </item>
        <item>
            <title>Recurrent intracranial solitary fibrous tumor initially diagnosed as hemangiopericytoma</title>
            <link>http://www.medworm.com/index.php?rid=643666&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv93xl15440g81575%2F</link>
            <description>We describe a case of an intracranial solitary fibrous tumor that recurred three times consecutively in an 11-year period.
 A 72-year-old man presented with a headache and gait disturbance. Magnetic resonance imaging (MRI) revealed a dumbbell tumor
 at the left tentorium. The tumor was removed but recurred. The first diagnosis was hemangiopericytoma, but all specimens showed
 a “patternless pattern” and few reticulin fibers, which features were not compatible with hemangiopericytoma. All tumors showed
 immunoreactivity for CD34 and bcl-2. These results point to a solitary fibrous tumor (SFT) and not to hemangiopericytoma.
 We present here a hypercellular spindle-cell tumor that was very similar to hemangiopericytoma but is better diagnosed as
 SFT.
 
	Content TypeJournal Article

	
		J...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=643666</comments>
            <pubDate>Sat, 26 May 2007 14:36:09 +0100</pubDate>
            <guid isPermaLink="false">643666</guid>        </item>
        <item>
            <title>Ectopic recurrence of dysplastic gangliocytoma of the cerebellum (Lhermitte–Duclos disease): a case report</title>
            <link>http://www.medworm.com/index.php?rid=643664&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl321418x75332089%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Lhermitte–Duclos disease is a rare clinical entity characterized by slow deformation of the cerebellar lesion. A 53-year-old
 woman presented with Lherimitte–Duclos disease manifesting as ataxic gait, occipital headache, and loss of consciousness.
 Magnetic resonance imaging demonstrated striated and laminar pattern lesions in the right cerebellar hemisphere and vermis.
 She underwent subtotal removal of the vermis compressing the brainstem, but the cerebellar hemisphere appeared normal and
 was preserved. Histological findings were consistent with Lherimitte–Duclos disease. Two years later, magnetic resonance imaging
 revealed enlargement of the right hemispheric lesion. Intraoperative appearance of the hemisphere demonstrated marked enlargement
 of the folia. Su...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=643664</comments>
            <pubDate>Sat, 26 May 2007 14:36:05 +0100</pubDate>
            <guid isPermaLink="false">643664</guid>        </item>
        <item>
            <title>FISH 1p/19q deletion/imbalance for molecular subclassification of glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=643668&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc0p714426k14h360%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioblastoma is the most malignant and frequent of the glial tumors. A minor fraction of glioblastoma may contain areas showing
 oligodendroglioma-like tumor cell differentiation. Several authors have described such tumors as glioblastoma with oligodendroglial
 component (GBMO). GBMO may represent the ultimate level of malignancy in the oligodendroglial lineage. The oligodendroglial
 component and combined loss of chromosomal arm 1p and 19q in glioblastoma indicate increased survival. In our study, we analyzed
 1p and 19q status in a series of 12 glioblastoma and 8 oligodendroglial tumors using fluorescence in situ hybridization (FISH)
 on paraffin-embedded tissues. In each case, hybridization status was classified as deletion, imbalance, polysomy, amplification,
 or no...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=643668</comments>
            <pubDate>Sat, 26 May 2007 14:36:01 +0100</pubDate>
            <guid isPermaLink="false">643668</guid>        </item>
        <item>
            <title>Early effects of boron neutron capture therapy on rat glioma models</title>
            <link>http://www.medworm.com/index.php?rid=643663&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F427841w0tt8ut10n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Early effects of boron neutron capture therapy (BNCT) on malignant glioma are characterized by reduction of the enhancement
 area and regression of the peritumoral edema radiologically. The aim of this study was to investigate the early histological
 changes of tumors and inflammatory cells after BNCT in the rat brain. Rats were treated with BNCT using boronophenylalanine
 (BPA) 7 days after implantation of C6 glioma cells. The tumors were assessed with magnetic resonance imaging and histopathological
 examination at 4 days after BNCT. The mean tumor volumes were 39 2 mm3 in the BNCT group and 134 18 mm3 in the control group. In the BNCT group, tumor cells showed a less pleomorphic appearance with atypical nuclei and mitotic
 figures. The Ki-67 labeling index was 6....</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=643663</comments>
            <pubDate>Sat, 26 May 2007 14:35:55 +0100</pubDate>
            <guid isPermaLink="false">643663</guid>        </item>
        <item>
            <title>A rare case of extraventricular neurocytoma</title>
            <link>http://www.medworm.com/index.php?rid=643667&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu37755q2w2307606%2F</link>
            <description>We report an unusual case of extraventricular (cerebral) neurocytoma with a long, 25-year history, and which appeared to transform
 to neuroblastoma. In 1978, an 18-year-old woman was treated for right frontal oligodendroglioma. Eighteen years later (in
 1996), recurrence of tumor in the fourth ventricle was noted and was treated with gamma-knife radiotherapy. The tumor shrunk
 transiently, but 7 years later (in 2004), MRI study demonstrated a second recurrence and ventricular dissemination. Partial
 removal was performed, and histological examination revealed that tumor cells had round or oval nuclei with halos. Frequent
 mitoses and vascular proliferation were observed. The MIB-1 LI was 80%. Despite postoperative whole-brain radiotherapy to
 a total dose of 30 Gy, the tumor progressed,...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=643667</comments>
            <pubDate>Sat, 26 May 2007 14:35:53 +0100</pubDate>
            <guid isPermaLink="false">643667</guid>        </item>
        <item>
            <title>Supratentorial ectopic cortical ependymoma occurring with intratumoral hemorrhage</title>
            <link>http://www.medworm.com/index.php?rid=643662&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk2823110l31v5221%2F</link>
            <description>We report here a rare case of supratentorial ectopic cortical ependymoma. This tumor was localized in the left angular gyrus,
 occurred with intratumoral hemorrhage, was attached to the dura mater, exhibited no continuity with the ventricular system,
 showed distinctive pathological features (perivascular pseudo-rosette formations and firework-like giant rosette formations),
 and finally transformed to a glioblastoma-like high-grade lesion. A cortical ependymoma should be considered in the differential
 diagnosis of supratentorial cortical tumors with intraparenchymal hemorrhage and high vascularity, even if not in contact
 with the ventricular system. Although malignant transformation is unusual in cortical ependymoma, close observation and adjunctive
 radiotherapy are strongly recommende...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=643662</comments>
            <pubDate>Sat, 26 May 2007 14:35:50 +0100</pubDate>
            <guid isPermaLink="false">643662</guid>        </item>
        <item>
            <title>Two cases of ringlike enhancement on MRI mimicking malignant brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=243439&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft81372542g432177%2F</link>
            <description>Abstract  The present study was performed to investigate two cases with ringlike enhanced lesions mimicking malignant tumors on magnetic
 resonance imaging (MRI) and to determine the utility of thallium-201 single-photon emission tomography (201Tl-SPECT) and diffusion-weighted MR imaging (DWI) for differential diagnosis between neoplastic and nonneoplastic lesions.
 One patient was a 50-year-old man who presented with a right caudate lesion. The 201Tl-SPECT study revealed no uptake in the lesion. Stereotactic biopsy was performed, and pathological findings indicated cerebral
 infarction. The other patient was a 58-year-old woman who presented with a right frontal lesion with edema. DWI showed a hypointense
 signal, and the apparent diffusion coefficient (ADC) revealed a hyperintense sign...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=243439</comments>
            <pubDate>Thu, 19 Oct 2006 07:54:32 +0100</pubDate>
            <guid isPermaLink="false">243439</guid>        </item>
        <item>
            <title>A case of tanycytic ependymoma arising from the cerebral hemisphere</title>
            <link>http://www.medworm.com/index.php?rid=243437&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F31868577g767713x%2F</link>
            <description>We report a rare case of tanycytic ependymoma arising from the cerebral hemisphere. A 59-year-old man was admitted to our
 hospital because of the incidental detection by MRI of a tumor lesion in the right temporooccipital paratrigonal region. The
 mass showed low-to iso-intensity on T1-weighted images and high intensity on T2/proton-weighted images. Partial resection was performed using a transsulcal approach to avoid compromising the visual field.
 Most of the tumor cells showed elongated spindle shapes arranged in dense fascicles. A few true ependymal rosettes and perivascular
 pseudorosettes were visible. The tumor cells were positive for GFAP, S-100, and vimentin, but negative for synaptophysin,
 EMA, and keratin. The MIB-1 labeling index was approximately 1%. Ultrastructurally, the t...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=243437</comments>
            <pubDate>Thu, 19 Oct 2006 07:54:32 +0100</pubDate>
            <guid isPermaLink="false">243437</guid>        </item>
        <item>
            <title>Mixed germ cell tumors with abundant sarcomatous component in the temporal lobe after radiochemotherapy of neurohypophyseal germinoma: a case report</title>
            <link>http://www.medworm.com/index.php?rid=243441&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fau781h4160846385%2F</link>
            <description>We report a case of intracranial germ cell tumor that showed pathological changes from neurohypophyseal germinoma to mixed
 germ cell tumors consisting exclusively of undifferentiated sarcomatous component after radiochemotherapy. Three surgical
 specimens and autopsied brain from the patient were histologically examined. An initial specimen from the neurohypophyseal
 tumor was diagnosed as germinoma with a two-cell pattern. Five years later, after repeated radiochemotherapy, the second specimen
 resected from the right temporal lobe showed mixed germ cell tumors consisting of the three components of germinoma, choriocarcinoma,
 and immature teratoma. Six months later after intensive radiotherapy, the right temporal tumor recurred and was surgically
 removed. The histological diagnosis was...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=243441</comments>
            <pubDate>Thu, 19 Oct 2006 07:54:31 +0100</pubDate>
            <guid isPermaLink="false">243441</guid>        </item>
        <item>
            <title>Prognostic implication of p27 expression in primary central nervous system lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=243436&amp;cid=s_33459_25_f&amp;fid=33459&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj3744132uv156g72%2F</link>
            <description>Abstract  To clarify the role of p27/Kip1 (p27) in primary central nervous system lymphomas (PCNSLs), we examined p27 expression by
 immunohistochemical methods in a series of 22 patients with PCNSL. We attempted to correlate the expression of p27 with proliferation
 potential and prognosis. Although the MIB-1 labeling index (LI) was lower in tumors with low p27 expression (26.7% ± 17.2%
 vs 38.1% ± 16.3%), it was not significantly different from that of tumors with high p27 expression (P = 0.1253). Survival analysis revealed that high p27 expression was significantly associated with poorer overall prognosis
 (P = 0.0011); however, the MIB-1 LI were not associated with prognosis. Our results suggest p27 as a predictor of prognosis
 in patients with PCNSL.
 
	Content TypeJournal Article...</description>
            <author>Brain Tumor Pathology</author>
            <type>journals</type>
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            <pubDate>Thu, 19 Oct 2006 07:54:31 +0100</pubDate>
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