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        <title>Neuro-Chirurgie 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 'Neuro-Chirurgie' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Neuro-Chirurgie&t=Neuro-Chirurgie&s=Search&f=source]]></link>
        <lastBuildDate>Sat, 04 Feb 2012 03:35:33 +0100</lastBuildDate>
        <item>
            <title>[Rebleeding from a vertebral artery dissection in a child: an inflammatory vasculopathy?]</title>
            <link>http://www.medworm.com/index.php?rid=5534522&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22154422%26dopt%3DAbstract</link>
            <description>We present a case of a rebleeding remote from a vertebral artery dissection associated with subarachnoid haemorrhage. A 7-year-old boy without any antecedent presented a traumatic dissection of the vertebral artery with subarachnoid haemorrhage. After a conservative treatment, the morphology of the vertebral artery became normal and the boy was asymptomatic. Four months later, a rebleeding occurred on the same vertebral artery, whose morphological review was normal. Mechanisms and cases of rebleeding in the literature are discussed. An inflammatory vasculopathy was suspected and discussed.
    PMID: 22154422 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5534522</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>[Chronic subdural hematoma infected by Campylobacter fetus: Case report.]</title>
            <link>http://www.medworm.com/index.php?rid=5534521&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22154423%26dopt%3DAbstract</link>
            <description>We report here a rare case of chronic subdural hematoma infected by Campylobacter fetus in a 86-year-old woman. She was admitted for confusion and disorientation in a context of high fever and diarrhoea. After two surgeries, the evolution was finally good with a combination of antibiotics (amoxicillin and clindamycin). Chronic subdural hematoma is a potential site for bacterial infection. Our case suggests that C. fetus infection should be suspected in elderly patients presenting with fever and enteritis. The frequency of such cases may be underestimated, due to the difficult diagnosis of C. fetus. It is also suspected that C. fetus could play a role in the recurrence of hematoma, because of its vessel tropism.
    PMID: 22154423 [PubMed - as supplied by publisher] (Source: Neuro-Chirur...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5534521</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5534521</guid>        </item>
        <item>
            <title>[Solitary intrasellar plasmocytoma revealed by a diplopia: A case report.]</title>
            <link>http://www.medworm.com/index.php?rid=5419865&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22088574%26dopt%3DAbstract</link>
            <description>CONCLUSION: Plasmocytomas of the cranial base revealing a myeloma represent a very rare entity. Nevertheless, whether solitary or multiple, a plasmocytoma must be considered amongst the differential diagnoses in the face of any invasive lesion of the sphenoid sinus.
    PMID: 22088574 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5419865</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5419865</guid>        </item>
        <item>
            <title>[Surgical anatomy of the lateral ventricles.]</title>
            <link>http://www.medworm.com/index.php?rid=5379648&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22036149%26dopt%3DAbstract</link>
            <description>Authors: Lejeune JP, Baroncini M, Peltier J, Le Gars D
    Abstract
    The lateral ventricle is a deep-seated cavity, overlayed by a cortical mantle which contains eloquent areas, especially on the dominant hemisphere, and surrounded by the optic radiations. The surgical approach requires a thorough preoperative reflexion based on magnetic resonance imaging, in order to understand the site of origin and the vascular pedicles of the tumor. Surgical approaches to the frontal horn, temporal horn and atrium are successively described.
    PMID: 22036149 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379648</comments>
            <pubDate>Thu, 27 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379648</guid>        </item>
        <item>
            <title>[Tumors of the lateral ventricle. Review of 284 cases.]</title>
            <link>http://www.medworm.com/index.php?rid=5379650&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22032889%26dopt%3DAbstract</link>
            <description>Authors: Baroncini M, Peltier J, Le Gars D, Lejeune JP
    Abstract
    The data from 284 cases of lateral ventricle (VL) tumors treated in 18 departments of Neurosurgery in France between 1995 and 2010 were collected in this series. The mean age was 33 years with a large proportion of children (79/284). CLINICAL PRESENTATION: The mean duration of symptoms was short in time (2 months). The revelation was incidental in 10% of the cases ; for symptomatic lesions, raised intracranial pressure (ICP, due to hydrocephalus) and neuropsychological signs were the most frequent. Only one third of the patients had no CSF disorder. HISTOPATHOLOGY: The two most frequent tumors were meningiomas (40 cases, 15%) and neurocytomas (35 cases, 13%). The sub-ependymal giant cells astrocytomas, the ependymomas...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379650</comments>
            <pubDate>Wed, 26 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379650</guid>        </item>
        <item>
            <title>[Anatomy of the periventricular white matter.]</title>
            <link>http://www.medworm.com/index.php?rid=5379651&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22032888%26dopt%3DAbstract</link>
            <description>Authors: Peltier J, Nicot B, Baroncini M, Zunon-Kipré Y, Haidara A, Havet E, Foulon P, Page C, Lejeune JP, Le Gars D
    Abstract
    The lateral ventricle (LV) has a deep position within the cerebral hemisphere. The LV is covered by white matter with important functional role in the dominant hemisphere. Lateral wall of the frontal horn is covered by the inferior occipitofrontal fasciculus (IOFF) and its roof by the corpus callosum (CC). The body of the LV has the same cranial relationship and is covered laterally by fibers of internal capsula and arcuate fasciculus; its lower part is in relationship with the body of the fornix. The atrium of the LV is covered by the arcuate fasciculus and its lower part is covered by the IOFF and optic radiations. The inferior horn or temporal horn is co...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379651</comments>
            <pubDate>Tue, 25 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379651</guid>        </item>
        <item>
            <title>[Conclusion.]</title>
            <link>http://www.medworm.com/index.php?rid=5379649&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22032890%26dopt%3DAbstract</link>
            <description>Conclusion.]
    Neurochirurgie. 2011 Oct 25;
    Authors: Lejeune JP, Le Gars D
    PMID: 22032890 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379649</comments>
            <pubDate>Tue, 25 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379649</guid>        </item>
        <item>
            <title>[Subependymomas of lateral ventricle. Analysis of our series and review of literature.]</title>
            <link>http://www.medworm.com/index.php?rid=5379663&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030163%26dopt%3DAbstract</link>
            <description>Authors: Peltier J, Lejeune JP, Nicot B, Capel C, Baroncini M, Fichten A, Toussaint P, Desenclos C, Lefranc M, Le Gars D
    Abstract
    Subependymoma is a benign lesion, slow-growing neoplasm, representing 0.2 to 0.7 % of intracranial tumors. They are often clinically silent, incidentally discovered at autopsy. These symptoms are related to big volume. They are attached to the septum pellucidum, leading to hydrocephalus by Monro foramen obstruction. Overall mean age at diagnosis is 39 years with more males than females. At CT-scan, subependymoma shows a slightly low attenuation compared to gray matter. There is no or mild enhancement following contrast injection. On MR T1-weighted imaging, subependymoma is isointense and hyperintense on MR T2-weighted imaging. Intramural calcification...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379663</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379663</guid>        </item>
        <item>
            <title>[Fundamental embryology and anatomy of the lateral ventricle.]</title>
            <link>http://www.medworm.com/index.php?rid=5379662&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030164%26dopt%3DAbstract</link>
            <description>Authors: Baroncini M, Peltier J, Lejeune JP, Le Gars D
    Abstract
    The lateral ventricles are the C-shaped cavities of the telencephalon. Embryology of theses cavities is recalled as well as the immediate relationship of the frontal horn, the body, the atrium and the temporal and occipital horns.
    PMID: 22030164 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379662</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379662</guid>        </item>
        <item>
            <title>[Rare tumors of the lateral ventricle. Review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=5379661&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030165%26dopt%3DAbstract</link>
            <description>Authors: Peltier J, Capel C, Nicot B, Baroncini M, Fichten A, Toussaint P, Desenclos C, Lefranc M, Le Gars D, Lejeune JP
    Abstract
    Metastases of lateral ventricle (LV) are attached to choroidal plexus. Primary source is cancer of kidney. Two thirds of patients are male. Oligodendrogliomas occur in young females. Signs of increased intracranial pressure are a constant feature. These tumors are found in anterior portion of the LV with severe enhancement and clumped calcifications. Treatment is surgical. Cavernomas have a preponderance of rapid growth with a bleeding revelation. Seizures are rare. Rebleeding is frequent and justifies a surgical treatment. Schwannomas are a rare entity in which the majority of patients are very young. MRI shows calcifications, cystic components and a st...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379661</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379661</guid>        </item>
        <item>
            <title>[Meningiomas of the lateral ventricle. A series of 40 cases with analysis of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=5379660&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030166%26dopt%3DAbstract</link>
            <description>Authors: Baroncini M, Peltier J, Le Gars D, Lejeune JP
    Abstract
    This series reports 40 cases of meningiomas of the lateral ventricle treated in France between 1995 and 2010. The mean age was 52 years. The revelation was incidental in 23% of cases. 36 patients underwent surgery with uneventful postoperative course in 75% of them. Visual field deficits were the most frequent sequelae. In six cases, recurrences occurred during the follow-up period. The relevant series of the literature were discussed in order to precise the therapeutic strategies and the outcome.
    PMID: 22030166 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379660</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379660</guid>        </item>
        <item>
            <title>[Neuroepithelial thalamo-mesencephalic cyst.]</title>
            <link>http://www.medworm.com/index.php?rid=5379659&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030167%26dopt%3DAbstract</link>
            <description>We describe a 42-year-old woman who presented with thalamic syndrome due to a neuroepithelial cyst of the thalamo-midbrain. Differential diagnosis is made with other cystic lesions in the brain. However a good analysis of imaging feature led to diagnosis. When the lesion is symptomatic, mini-invasive procedure is indicated.
    PMID: 22030167 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379659</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379659</guid>        </item>
        <item>
            <title>Illustration of the impact of antiplatelet drugs on the genesis and management of chronic subdural hematoma.</title>
            <link>http://www.medworm.com/index.php?rid=5379658&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030168%26dopt%3DAbstract</link>
            <description>Authors: Mascarenhas L
    Abstract
    The case of a 76-year-old male with a large chronic subdural hematoma that showed total regression with the mere suspension of aspirin, its only apparent causal factor, and that of an 81 year-old male on aspirin and clopidogrel with a chronic subdural hematoma who succumbed after burr holes due to two simultaneous severe hemorrhagic complications (cerebellar hemorrhage and ipsilateral acute subdural hematoma) are presented. The cases may provide support for the following management strategies: (i) if conservative management and drug suspension are feasible, they may well be worth trying and lead to a favorable outcome; (ii) if a patient is at risk of developing a chronic subdural hematoma, namely because of a minor acute subdural hematoma, withdrawal...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379658</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379658</guid>        </item>
        <item>
            <title>[Introduction.]</title>
            <link>http://www.medworm.com/index.php?rid=5379657&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030169%26dopt%3DAbstract</link>
            <description>Authors: Le Gars D, Lejeune JP
    PMID: 22030169 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379657</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379657</guid>        </item>
        <item>
            <title>[Clinical and ossification outcome of custom-made hydroxyapatite prothese for large skull defect.]</title>
            <link>http://www.medworm.com/index.php?rid=5379656&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030170%26dopt%3DAbstract</link>
            <description>DISCUSSION: Hydroxyapatite custom-made implants for cranioplasty appear to be ideal for good aesthetic and tolerance results, but their ossification is hardly analyzed due to the prosthesis density higher than the bone's density. This is why we recommend them for children and in cases of complex defects such as pterion location.
    PMID: 22030170 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379656</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379656</guid>        </item>
        <item>
            <title>[Pathological aspects of the tumors of the lateral ventricles.]</title>
            <link>http://www.medworm.com/index.php?rid=5379655&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030171%26dopt%3DAbstract</link>
            <description>Authors: Maurage CA, Sevestre H
    Abstract
    Typing a tumor of the lateral ventricle is often an issue, even for an experienced Neuropathologist. In this location are encountered specific entities, such as neurocytoma and subependymal giant cell astrocytoma, as well as more usual tumors, displaying a common misleading morphology, for instance a main clear cell component. The panel of diagnostic tools given to the pathologists has been increasing for a few years, enriched by immunohistochemical and molecular probes.
    PMID: 22030171 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379655</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379655</guid>        </item>
        <item>
            <title>Mature posterior fossa teratoma mimicking infratentorial meningioma: A case report.</title>
            <link>http://www.medworm.com/index.php?rid=5379654&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030172%26dopt%3DAbstract</link>
            <description>We report a case of mature posterior fossa teratoma in an adult patient diagnosed in the 4th decade of life. This lesion was taken for a huge infratentorial meningioma.
    PMID: 22030172 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379654</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379654</guid>        </item>
        <item>
            <title>[Ependymomas of the lateral ventricle. A series of 27 cases with review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=5379653&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030173%26dopt%3DAbstract</link>
            <description>Authors: Lejeune JP, Reyns N, Baroncini M, Peltier J, Le Gars D
    Abstract
    Twenty-seven cases of ependymoma were collected in the French multicentric study dedicated to lateral ventricle tumors. The mean age of patients was 31,5 years. All patients underwent surgery, with complete resection of the tumor in 76% of cases. Histologic examination disclosed 23 grade 2 ependymomas and four grade 3 ependymomas. Postoperative mortality was 7%. Four patients underwent radiotherapy, and five chemotherapy. Local recurrence of the tumor occurred in seven cases, with a mean delay of 48 months. Disseminated disease within the central nervous system was found in only one patient. Median survival in all the 27 patients was 181 months, and median progression-free survival was 106 months. The relevant...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379653</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379653</guid>        </item>
        <item>
            <title>[Arteries and veins of the lateral ventricle.]</title>
            <link>http://www.medworm.com/index.php?rid=5379652&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22030174%26dopt%3DAbstract</link>
            <description>Authors: Peltier J, Baroncini M, Zunon-Kipré Y, Haidara A, Havet E, Foulon P, Page C, Lejeune JP, Le Gars D
    Abstract
    Tumors of the frontal horn of the lateral ventricle (LV) are only supplied by the posteromedial choroidal artery. Tumors of the body of the LV are supplied by the same artery. Tumors of the atrium of the LV with anterior extension are supplied by both posteromedial choroidal and posterolateral arteries. Tumors of the atrium with inferior extension are supplied by both anterior choroidal artery and posterolateral choroidal arteries. Tumors of the inferior horn are only supplied by anterior choroidal artery. The tumoral venous drainage is organized with three main groups of veins : a medial group, a lateral group and a choroidal group.
    PMID: 22030174 [PubMed - as...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379652</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379652</guid>        </item>
        <item>
            <title>[Tumors of the lateral ventricle in child: Characteristics and specificities.]</title>
            <link>http://www.medworm.com/index.php?rid=5379665&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22024608%26dopt%3DAbstract</link>
            <description>Authors: Vinchon M, Baroncini M, Leblond P
    Abstract
    Tumors of the lateral ventricle are not as rare in children as in adults and present complex problems which are to be dealt with often in a context of emergency, on account of their large size and the risk of life-threatening bleeding in a small child. Their diagnostic features are different in children, especially in infants and even more so in the fetus. The main surgical problems are the risk of bleeding and of hydraulic complications. From an oncological perspective, the main tumor types are choroid plexus tumors, subependymal giant-cell astrocytoma, and low-grade gliomas. The developmental outcome of these patients is often poor, on account of severe intracranial hypertension and young age at diagnosis.
    PMID: 22024608 [Pu...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379665</comments>
            <pubDate>Sat, 22 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379665</guid>        </item>
        <item>
            <title>[Place of stereotactic techniques in the modern management of lateral ventricle tumors. Stereotactic biopsies and radiosurgery.]</title>
            <link>http://www.medworm.com/index.php?rid=5379664&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22024609%26dopt%3DAbstract</link>
            <description>Authors: Lefranc M, Reyns N, Blond S
    Abstract
    The authors make an overview about the use of stereotactic techniques in the management of lateral ventricle tumors. If stereotactic techniques are not in the foreground for the management of lateral ventricle tumors, stereotactic biopsies can be very useful in case of atypical, clinical or radiological presentation of the tumors and radiosurgery can help in case of evolution or re-evolution of tumors after resection. In these cases, stereotactic procedures are very safe. Modern technical evolutions allow the optimization of the stereotactic procedure but also to mix robotic with endoscopic techniques in order to offer new surgical perspectives.
    PMID: 22024609 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379664</comments>
            <pubDate>Sat, 22 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379664</guid>        </item>
        <item>
            <title>[Imaging of lateral ventricle tumors.]</title>
            <link>http://www.medworm.com/index.php?rid=5379667&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22019219%26dopt%3DAbstract</link>
            <description>Authors: Delmaire C, Boulanger T, Leroy HA, Tempremant F, Pruvo JP
    Abstract
    Lateral ventricular neoplasms are rare, and account for 50% of all intraventricular tumors in adults and 25% in children. Although these neoplasms are easily detected with computed tomography (CT) and magnetic resonance imaging (MRI), both techniques are relatively unspecific in identifying the type of tumor. However, few imaging patterns are specific for a particular pathological process and useful conclusions can be made from the morphological appearance of the lesion, its location and enhancement pattern. The aim of this article was to review and illustrate the CT and MRI findings of a wide spectrum of tumors of the lateral ventricle. We reviewed choroid plexus tumors, meningioma, subependymal giant cell...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379667</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379667</guid>        </item>
        <item>
            <title>[Central neurocytomas of the lateral ventricle. A series of 35 cases with review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=5379666&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22019220%26dopt%3DAbstract</link>
            <description>Authors: Peltier J, Baroncini M, Le Gars D, Lejeune JP
    Abstract
    Central neurocytoma is the second most frequent tumor in our series of 284 lateral ventricle tumors (12%). Mean age was 32.6 years. There was a male predominance (20/35). Most frequent clinical signs were neuropsychological disturbances and intracranial hypertension. On imaging, these tumors concentrate central calcifications in more than half of cases. Main locations were frontal horn and corpus of lateral ventricle (82%). Uneventful postoperative course was recorded in 52% of cases. Immunoreactivity against neuron-specific enolase (NSE), synaptophysin, S100 protein, Microtubul Associated Protein de type 2 (MAP2) and calcineurin confirms the neuronal nature of the neoplasm. This tumor has a good prognosis. Local cont...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379666</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379666</guid>        </item>
        <item>
            <title>[Anterior optic pathways compression by a surgical clip mobilized by delayed chronic hydrocephalus after treatment of a ruptured anterior communicating artery aneurysm.]</title>
            <link>http://www.medworm.com/index.php?rid=5327787&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21992996%26dopt%3DAbstract</link>
            <description>Authors: Zaïri F, Thines L, Bourgeois P, Ayachi M, Lejeune JP
    Abstract
    Chronic hydrocephalus is a classic and recognized complication that affects 6 to 37% of patients with aneurysmal subarachnoid haemorrhage. The diagnosis is often mentioned due to the delayed onset of gait disturbance and slower psychomotor performance. The CT-scan confirms the diagnosis by showing an enlargement of the ventricles. In case of symptomatic hydrocephalus, a ventriculo-peritoneal shunt is often required. The authors report a rare case of chronic hydrocephalus presenting with visual symptoms, due to the delayed mobilisation of a surgical clip with direct mass effect over the anterior optic pathways. The treatment of hydrocephalus led to a rapid and complete regression of symptoms.
    PMID: 21992996 ...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5327787</comments>
            <pubDate>Mon, 10 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5327787</guid>        </item>
        <item>
            <title>[Cervical chondrosarcoma: About two cases.]</title>
            <link>http://www.medworm.com/index.php?rid=5230135&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21917278%26dopt%3DAbstract</link>
            <description>We report two cases of cervical chondrosarcoma in two men aged respectively 70 and 40years. Symptomatology was cervicobrachial neuralgia and motor deficit. Both patients were operated and the treatment completed by radiotherapy.
    PMID: 21917278 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5230135</comments>
            <pubDate>Mon, 12 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5230135</guid>        </item>
        <item>
            <title>[Long-term outcome of patients treated with spinal cord stimulation for therapeutically refractory failed back surgery syndrome: A retrospective study.]</title>
            <link>http://www.medworm.com/index.php?rid=5218966&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21907361%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Our retrospective study demonstrates a satisfaction of 75% of the patients after 8.3-years follow-up. Spinal cord stimulation is an effective treatment for refractory failed back surgery syndrome.
    PMID: 21907361 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218966</comments>
            <pubDate>Thu, 08 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218966</guid>        </item>
        <item>
            <title>Superior interhemispheric approach for midline meningioma from the anterior cranial base.</title>
            <link>http://www.medworm.com/index.php?rid=5218965&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21907362%26dopt%3DAbstract</link>
            <description>CONCLUSION: The superior IH approach could be considered a safe anteriorly orientated midline approach for removal OGM and TSM meningioma.
    PMID: 21907362 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218965</comments>
            <pubDate>Thu, 08 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218965</guid>        </item>
        <item>
            <title>Spontaneous regression of a symptomatic atlanto-occipital joint cyst. Case report.</title>
            <link>http://www.medworm.com/index.php?rid=5218964&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21907363%26dopt%3DAbstract</link>
            <description>In this report, the authors describe an atlanto-occipital SC revealed by hypoglossal nerve palsy in a 75-year-old woman. Due to the paucity of neurological signs and the patient's advanced age, she was managed conservatively; 8months later the cyst resolved completely. We discuss the potential factors involved in the pathogenesis and the therapeutic options for this uncommon cervical entity. We advise conservative treatment as a first therapeutic option for SC without signs of spinal cord compression.
    PMID: 21907363 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218964</comments>
            <pubDate>Thu, 08 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218964</guid>        </item>
        <item>
            <title>[Orbital subperiotal hematoma associated with extradural hematoma: One case report.]</title>
            <link>http://www.medworm.com/index.php?rid=5218968&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21899862%26dopt%3DAbstract</link>
            <description>We report a case of an 8-year-old girl who presented after traumatism, a subperiotal hematoma of the orbit with two extradural hematomas. During the first clinical examination realized while the patient was unconscious, left exophthalmia was found, but after conscious improvement, we discovered ophtalmoplegia and a grade I papilla edema. The CT scan showed two extradural hematomas and a left intraorbital hematoma. The intraorbital hematoma was drained by surgical way but the extradural hematomas were not surgical. The outcome has been marked by the neurological improvement and the oculomotricity recovering.
    PMID: 21899862 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218968</comments>
            <pubDate>Mon, 05 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218968</guid>        </item>
        <item>
            <title>[Nasal dermoïd cyst with intracranial extension: Which approach?]</title>
            <link>http://www.medworm.com/index.php?rid=5218967&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21899863%26dopt%3DAbstract</link>
            <description>We report a case of a 2 years old patient who was operated for a nasal congenital cyst extending to the nasal septum. Anatomopathology showed a dermoïd cyst. Five years later, he presented local recurrence of the dermoïd cyst with intracranial extension through a bifid crista galli. We conclude that to avoid recurrence, the removal of the nasal cyst and sinus tract must be followed to its dural attachment. A transfacial approach can be associated with frontal craniotomy, which can provide adequate exposure for complete removal of the intracranial component of the cyst and sinus tract. A literature review was performed.
    PMID: 21899863 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218967</comments>
            <pubDate>Mon, 05 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218967</guid>        </item>
        <item>
            <title>[What should be done in the event of incidental meningioma?]</title>
            <link>http://www.medworm.com/index.php?rid=4807710&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21543093%26dopt%3DAbstract</link>
            <description>CONCLUSION: We recommend neurosurgical consultation for all patients with an incidental meningioma.
    PMID: 21543093 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4807710</comments>
            <pubDate>Sun, 01 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4807710</guid>        </item>
        <item>
            <title>[Cervical cord compression by hereditary multiple exostosis: Case report and review of literature.]</title>
            <link>http://www.medworm.com/index.php?rid=4807717&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21531431%26dopt%3DAbstract</link>
            <description>CONCLUSION: The cervical exostosis associated with HME is a rare disease. The clinical symptomatology is dominated by spinal cord compression and surgical treatment allows excellent clinical results.
    PMID: 21531431 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4807717</comments>
            <pubDate>Thu, 28 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4807717</guid>        </item>
        <item>
            <title>White matter anatomy of the human deep brain revisited with high resolution DTI fibre tracking.</title>
            <link>http://www.medworm.com/index.php?rid=4807722&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21530985%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Beyond to demonstrate the feasibility of imaging the deepest WM fascicles in vivo, our results pave the way for a better understanding of the brain connectivity and for developing targeted neuromodulation.
    PMID: 21530985 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4807722</comments>
            <pubDate>Wed, 27 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4807722</guid>        </item>
        <item>
            <title>[Endoscopic decompression of the ulnar nerve in the cubital tunnel syndrome: About 55 patients.]</title>
            <link>http://www.medworm.com/index.php?rid=4807719&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21530986%26dopt%3DAbstract</link>
            <description>CONCLUSION: Endoscopic decompression of the ulnar nerve in sulcus ulnaris syndrome is very well appreciated by patients and also provides promising clinical results.
    PMID: 21530986 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4807719</comments>
            <pubDate>Wed, 27 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4807719</guid>        </item>
        <item>
            <title>[Adjunctive use of endoscopy during microvascular decompression in the cerebellopontine angle: 27 case reports.]</title>
            <link>http://www.medworm.com/index.php?rid=4807718&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21530987%26dopt%3DAbstract</link>
            <description>Authors: Duntze J, Litré CF, Eap C, Théret E, Bazin A, Chays A, Rousseaux P
    Microvascular decompression is an important procedure for the management of microvascular compression syndromes in the cerebellopontine angle (CPA) like trigeminal neuralgia or hemifacial spasm. The ability to identify the offending vessel is the key to success. Can the endoscope help surgeons to identify and understand the responsible conflict in order to treat them? Our series concerns 27 consecutive patients who underwent microvascular decompression systematically using an endoscope with an angulation of 30° at the beginning and the end of the intervention. The decompression procedure was done under microscope. Endoscopic exploration was successful for all patients. Endoscopy improved visualization of the...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4807718</comments>
            <pubDate>Wed, 27 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4807718</guid>        </item>
        <item>
            <title>[Bilateral failure of fusion between pedicles and body of C7.]</title>
            <link>http://www.medworm.com/index.php?rid=4807723&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21529856%26dopt%3DAbstract</link>
            <description>Authors: Nicot B, Peltier J, Fichten A, Lefranc M, Desenclos C, Toussaint P, Le Gars D
    We expose the case of a 48-year-old woman suffering of a chronic bilateral C7 radiculalgy and bilateral C7 failure of fusion between pedicles and body. According to spine embryogenesis we bring three hypothesis to explain this failure of fusion. Then we show that bilateral C6-C7 foraminal compression can arise from local cervical spine instability due to C7 and disk development abnormalities. The treatment proposed is dissectomy bone graft and anterior osteosynthesis leading to clinical and radiological good results. The patient went back to work after three months.
    PMID: 21529856 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4807723</comments>
            <pubDate>Tue, 26 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4807723</guid>        </item>
        <item>
            <title>[Gilliatt-Sumner hand or true neurogenic thoracic outlet syndrome. A report on seven operated cases.]</title>
            <link>http://www.medworm.com/index.php?rid=4527797&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21333310%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Physicians' unfamiliarity with TOS diagnosis or their reluctance to accept the diagnosis without electrical confirmation can lead to hand atrophy. Brachial plexus decompression at this stage usually stabilizes the deficit.
    PMID: 21333310 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4527797</comments>
            <pubDate>Wed, 16 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4527797</guid>        </item>
        <item>
            <title>[Minimally invasive osteosynthesis in septic conditions.]</title>
            <link>http://www.medworm.com/index.php?rid=4527796&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21333311%26dopt%3DAbstract</link>
            <description>CONCLUSION: Percutaneous osteosynthesis in septic conditions in association with an anterior graft provides satisfactory clinical and radiographic results. It provides a valuable alternative for deformity correction and spinal stabilization with a minimally invasive access in patients with comorbidities.
    PMID: 21333311 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4527796</comments>
            <pubDate>Wed, 16 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4527796</guid>        </item>
        <item>
            <title>[Giant thoracolumbar synovial cyst: Case report.]</title>
            <link>http://www.medworm.com/index.php?rid=4406298&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21251687%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: In spite of a careful review of the literature, no other description of a giant thoracolumbar synovial cyst developed on three metameric levels was found. The diagnosis was made with a MRI scan combined with microscopic examination. The pathogenesis and therapeutic strategy are discussed.
    PMID: 21251687 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4406298</comments>
            <pubDate>Tue, 18 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4406298</guid>        </item>
        <item>
            <title>[Thoracic spine pseudarthrosis treated by transpleural corporectomy and bone morphogenic protein.]</title>
            <link>http://www.medworm.com/index.php?rid=4406299&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21247607%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: The use of bone morphogenic proteins might be of great help in rare but challenging cases of spinal pseudarthrosis, with a quick return to normal activity after a single-stage surgery.
    PMID: 21247607 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4406299</comments>
            <pubDate>Mon, 17 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4406299</guid>        </item>
        <item>
            <title>[A case of unilateral dislocation of C3 right facet joint treated with lateral mass plating.]</title>
            <link>http://www.medworm.com/index.php?rid=4186585&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21087778%26dopt%3DAbstract</link>
            <description>Authors: Ndoumbé A, Motah M, Mballa Amougou JC, Guifo Marc ML, Takongmo S, Sosso Maurice A
    Facet joint dislocations of the cervical spine are distractive-flexion injuries that account for 6 to 10 % of traumatic lesions of the subaxial cervical spine. Distractive-flexion injuries of the cervical spine were classified into four stages by Allen and Fergusson. These unstable lesions predominate at the fifth and sixth levels and all aspects of their management are subject to controversy, including their classification. Attempting reduction before surgery, performing MRI before or after closed reduction, choosing between surgery and external contention, the anterior versus the posterior approach are still matters of controversy between experts. The authors report a stage 2 distractive-fl...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4186585</comments>
            <pubDate>Tue, 16 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4186585</guid>        </item>
        <item>
            <title>[A case of cervical intradural extramedullary mature cystic teratoma: Diagnosis and management.]</title>
            <link>http://www.medworm.com/index.php?rid=4186584&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21087779%26dopt%3DAbstract</link>
            <description>We report an exceptional case of adult-onset intradural extramedullary teratoma of the cervical spinal cord and bulbomedullary junction with no evidence of spinal dysraphism and no history of previous spinal surgery and/or lumbar puncture. The patient was a 38-year-old woman whose chief complaint was progressive installation of a tetraparesis. Magnetic resonance imaging showed a cystic tumor on both sides of the foramen magnum compressing the bulbomedullary junction. The tumor was totally surgically resected. The histopathological diagnosis was a mature teratoma.
    PMID: 21087779 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4186584</comments>
            <pubDate>Tue, 16 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4186584</guid>        </item>
        <item>
            <title>[Rosai-Dorfman disease mimicking meningiomatosis: A case report.]</title>
            <link>http://www.medworm.com/index.php?rid=4186586&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21074226%26dopt%3DAbstract</link>
            <description>We report a case of RDD in a patient presenting multiple meningeal nodules with a review of the literature and discussion of differential diagnosis.
    PMID: 21074226 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4186586</comments>
            <pubDate>Wed, 10 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4186586</guid>        </item>
        <item>
            <title>[Thirty years of laser-assisted microvascular anastomosis (LAMA): What are the clinical perspectives?]</title>
            <link>http://www.medworm.com/index.php?rid=4139799&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21035824%26dopt%3DAbstract</link>
            <description>CONCLUSION: The first two clinical series using the 1.9-μm diode laser appear promising. Technical innovation will most likely lead to greater ease of use of the laser handpiece in the operating room.
    PMID: 21035824 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4139799</comments>
            <pubDate>Fri, 29 Oct 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4139799</guid>        </item>
        <item>
            <title>[Chemotherapy and targeted treatments in glioblastomas.]</title>
            <link>http://www.medworm.com/index.php?rid=4139800&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21035151%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Recent studies conducted in GBM, both in the adjuvant and recurrent setting, have changed the natural course of the disease and opened a new area of clinical research, including imaging and response evaluation, predictive markers, and other targeted therapies.
    PMID: 21035151 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4139800</comments>
            <pubDate>Wed, 27 Oct 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4139800</guid>        </item>
        <item>
            <title>[Conclusions: Glioblastomas. Standards, options, recommendations.]</title>
            <link>http://www.medworm.com/index.php?rid=4045149&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20884036%26dopt%3DAbstract</link>
            <description>Conclusions: Glioblastomas. Standards, options, recommendations.]
    Neurochirurgie. 2010 Sep 28;
    Authors: Paquis P, Menei P
    
    PMID: 20884036 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4045149</comments>
            <pubDate>Mon, 27 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4045149</guid>        </item>
        <item>
            <title>[Desmoplastic fibroma of the skull in an infant.]</title>
            <link>http://www.medworm.com/index.php?rid=4026895&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20880561%26dopt%3DAbstract</link>
            <description>We report a further case of a desmoplastic fibroma of the skull in a 3-year-old boy who presented with a right parietal mass. The CT scan showed a lytic mass with brain compression and cortical destruction. The patient underwent a craniectomy and complete mass resection. Histological diagnosis was desmoplastic fibroma. Postoperative progress was normal without recurrence 6Â months later.
    PMID: 20880561 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4026895</comments>
            <pubDate>Sun, 26 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4026895</guid>        </item>
        <item>
            <title>[The &quot;glioblastoma multiforme&quot;, 30 years later.]</title>
            <link>http://www.medworm.com/index.php?rid=4026894&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20880562%26dopt%3DAbstract</link>
            <description>[The &quot;glioblastoma multiforme&quot;, 30 years later.]
    Neurochirurgie. 2010 Sep 27;
    Authors: Chatel M
    
    PMID: 20880562 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4026894</comments>
            <pubDate>Sun, 26 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4026894</guid>        </item>
        <item>
            <title>[Clinical factors in glioblastoma and neuroradiology.]</title>
            <link>http://www.medworm.com/index.php?rid=4005862&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20870253%26dopt%3DAbstract</link>
            <description>Authors: Lonjon M, Mondot L, Lonjon N, Chanalet S
    Glioblastoma is found preferentially in men (1.5/1), nearing age 60, but all ages can be concerned. Clinical symptoms are intracranial mass without specificity, intracranial hypertension and localization signs. From the clinical history, the essential prognosis factors are: age, Karnofsky score and cognitive dysfunction. Conventional MRI sequences, including T1-FSE with and without contrast injection and T2-FSE or Flair-weighted sequences, provide the diagnosis in most cases, showing an intraparenchymal mass with a heterogeneous, irregularly enhanced signal. Other sequences define the tumor more precisely. Diffusion sequences provide the differential diagnosis with an abscess or a highly cellular tumor such as lymphoma. Perfusion sequen...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005862</comments>
            <pubDate>Thu, 23 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005862</guid>        </item>
        <item>
            <title>[Glioblastoma incident studies from May 2006 to May 2007 in Angers and Nice, France.]</title>
            <link>http://www.medworm.com/index.php?rid=4005861&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20870254%26dopt%3DAbstract</link>
            <description>This study was conducted 2 years after the audit on incident glioblastoma in France in 2004. New events that may modify the care or survival of glioblastoma have occurred since 2004, justifying the present study. The results show that the Karnowsky Index is more often included in the clinical files and that the rate of complete resection has increased, indicating that neurosurgeons are becoming aware of neuro-oncology. Patients with total resection still have the longest survival (14 months). Surprisingly, less than half the patients having surgery received concomitant radiochemotherapy according to the Stupp protocol. Median overall survival remains at 9 months with intention to treat. For patients treated with concomitant chemoradiotherapy with temozolomide, the median survival is 12 mon...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005861</comments>
            <pubDate>Thu, 23 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005861</guid>        </item>
        <item>
            <title>[Usefulness of botulinum toxin injections in the treatment of postoperative pain after cervical spine surgery: Preliminary results.]</title>
            <link>http://www.medworm.com/index.php?rid=4005860&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20870255%26dopt%3DAbstract</link>
            <description>CONCLUSION: Regardless of its limitations, the present study would seem to show potential value in the use of botulinum toxin in the treatment of postoperative pain after cervical spinal surgery.
    PMID: 20870255 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005860</comments>
            <pubDate>Thu, 23 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005860</guid>        </item>
        <item>
            <title>[Intradiploic cavernous hemangioma of the calvaria: Case report and review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=4005859&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20870256%26dopt%3DAbstract</link>
            <description>We report the case of a 31-year-old patient who had had frontal cephalalgias for several years. CT and MRI anatomical imaging objectified a frontal osteolytic tumor respecting the osseous external table but compressing the superior sagittal sinus. Total en bloc resection of the tumor associated with titan cranioplasty was performed. The postoperative course was uneventful. Three months after surgery the patient no longer reported headache. The anatomical and pathological results concluded in intradiploic cavernous hemangioma. We discuss this case and others described in the literature.
    PMID: 20870256 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005859</comments>
            <pubDate>Thu, 23 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005859</guid>        </item>
        <item>
            <title>[Reconstruction of the cranial vault using CAD/CAM-fabricated glass bioceramic implants.]</title>
            <link>http://www.medworm.com/index.php?rid=4005858&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20870257%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: CAD/CAM-fabricated Bioverit(Â®)Â II prostheses are a good alternative when autologous bone is not available. Fabrication of bioceramic prostheses using this method requires surgical scheduling, which is justified by the following advantages: reduced operating time, lack of donor morbidity, good esthetic results, and stability. The only drawback of this material is its price, which can limit its deployment.
    PMID: 20870257 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005858</comments>
            <pubDate>Thu, 23 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005858</guid>        </item>
        <item>
            <title>[Surgical treatment of glioblastomas.]</title>
            <link>http://www.medworm.com/index.php?rid=4005866&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869732%26dopt%3DAbstract</link>
            <description>Authors: Menei P, Metellus P
    Although the need for glioblastoma surgery to confirm the histology and decrease the mass effect, and therefore the symptoms, is recognized, the value of total resection remains controversial. In practice, the resected glioblastoma ratio is low. Of 952Â glioblastomas treated in France in 2004, 56% were resected and 44% biopsied. An analysis of the literature confirms the importance of resection on survival. Perioperative drugs, surgical techniques, as well as intra- and postoperative imaging are analyzed in view of the literature.
    PMID: 20869732 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005866</comments>
            <pubDate>Wed, 22 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005866</guid>        </item>
        <item>
            <title>[Epidemiology of glioblastoma.]</title>
            <link>http://www.medworm.com/index.php?rid=4005865&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869733%26dopt%3DAbstract</link>
            <description>Authors: Baldi I, Huchet A, Bauchet L, Loiseau H
    An increasing incidence of glioblastoma has been observed over the last 30 years. Improvements in diagnostic tools such as CT scans and MRI, changes observed in histological classifications, and adjustments in neurosurgical practices have contributed substantially to this increase. Moreover, the aging of the population and the increasing occurrence of glioblastoma beyond 60 years of age are additional explanations. In Gironde (France), where a specialized registry has been established, the annual incidence of glioblastoma is 4.96/100,000. Wide geographic variations are observed, possibly linked to ethnicity. However, the role of intrinsic and/or extrinsic factors cannot be ruled out. Comparing data between registries is difficult and req...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005865</comments>
            <pubDate>Wed, 22 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005865</guid>        </item>
        <item>
            <title>[Genetic diseases and glioblastomas.]</title>
            <link>http://www.medworm.com/index.php?rid=4005864&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869734%26dopt%3DAbstract</link>
            <description>Authors: Almairac F, Frenay M, Paquis P
    Some cancers are involved in inherited genetic syndromes. These genetic diseases are suspected of being involved in approximately 1% of gliomas. Few data are available on glioblastomas and their characteristics among these diseases. Familial syndromes known to predispose individuals to glioblastoma are neurofibromatosis typeÂ 1, Li-Fraumeni's syndrome, tuberous sclerosis, and Turcot's syndrome. This review discusses glioblastomas related to these diseases and the current knowledge on the statistical, clinical, and molecular biology data. Non-syndromic glioma families are discussed: a better understanding of molecular abnormalities in these groups should help understand the mechanisms of gliomagenesis. A case of malignant glioma requires the phy...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005864</comments>
            <pubDate>Wed, 22 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005864</guid>        </item>
        <item>
            <title>[Local antitumor treatments.]</title>
            <link>http://www.medworm.com/index.php?rid=4005863&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869735%26dopt%3DAbstract</link>
            <description>Authors: Menei P, Metellus P
    The idea of intraoperative adjuvant treatment is not new. This review describes only the strategies studied in phaseÂ III clinical trials. Among these strategies, only Gliadel(Â®) obtained marketing authorization. Some immunotoxins, administered by convection-enhanced delivery, and a gene therapy approach using an adenovirus went through a phaseÂ II trial and are currently being studied in a phaseÂ III trial. Brachytherapy has never been validated by a clinical trial.
    PMID: 20869735 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005863</comments>
            <pubDate>Wed, 22 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005863</guid>        </item>
        <item>
            <title>[Introduction: Glioblastomas.]</title>
            <link>http://www.medworm.com/index.php?rid=4005871&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869087%26dopt%3DAbstract</link>
            <description>Authors: Paquis P, Menei P
    
    PMID: 20869087 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005871</comments>
            <pubDate>Tue, 21 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005871</guid>        </item>
        <item>
            <title>[Glioblastoma: Clinical, radiological and biological prognostic factors.]</title>
            <link>http://www.medworm.com/index.php?rid=4005870&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869088%26dopt%3DAbstract</link>
            <description>Authors: Fontaine D, Paquis P
    The main prognostic factors of glioblastomas (GBM) are age, neurological and cognitive status, frontal tumor location, extent of surgical resection, adjuvant therapies received, presence of IDH1Â mutations, and MGMT expression. Other molecular prognostic factors have been proposed, such as mutations of TP53Â and PTEN, amplification of EGFR, and deletion of 10q, but their prognostic values remain controversial. MGMT promotor gene methylation is correlated with higher chemosensitivity and consequently is a good prognostic factor only in patients treated with chemotherapy. In the future, the gene expression profile will probably be a stronger prognostic factor than histological grade, but the most relevant gene clusters, whose expression may be correlated...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005870</comments>
            <pubDate>Tue, 21 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005870</guid>        </item>
        <item>
            <title>[The mystery of prehistoric trepanations: Is neurosurgery the world eldest profession?]</title>
            <link>http://www.medworm.com/index.php?rid=4005869&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869089%26dopt%3DAbstract</link>
            <description>Authors: Chauvet D, Sainte-Rose C, Boch AL
    Trepanation is known to be the first surgical procedure ever performed. Its origins date from the Neolithic Age in Europe and the operation was particularly performed in South America at the Pre-Colombian era, a few thousand years later. Based on many archeological studies on trepanned skulls, we compare the differences and similarities of these two periods through epidemiological, topographical, and technical approaches. Signs of bony regeneration are assessed in an attempt to understand the postoperative survival of trepanned patients. The literature in surgery and archeology does not mention the possible relation between trepanations and growing skull fractures. However, it is reasonable to think that these cranial holes, occurring after a ...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005869</comments>
            <pubDate>Tue, 21 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005869</guid>        </item>
        <item>
            <title>[Radiotherapy in adult glioblastomas.]</title>
            <link>http://www.medworm.com/index.php?rid=4005868&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869090%26dopt%3DAbstract</link>
            <description>Authors: Bondiau PY, Fauchon F, Jadaud E, Paquis P
    Radiation therapy is a treatment of malignant gliomas in adults. It improves survival rates, whether used alone, in addition to surgery, or in combination with chemotherapy. Three-dimensional imaging techniques, image fusion, and conformational radiotherapy are optimizing treatment plans for the treatment of these tumors and are sparing healthy tissue. After a review of the physical and biological bases of ionizing radiation, we present the techniques, results, side effects, and results of irradiation of glioblastomas.
    PMID: 20869090 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005868</comments>
            <pubDate>Tue, 21 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005868</guid>        </item>
        <item>
            <title>[Classification of glioblastoma and genome profiling.]</title>
            <link>http://www.medworm.com/index.php?rid=4005867&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869091%26dopt%3DAbstract</link>
            <description>Authors: de Tayrac M, Mosser J
    
    PMID: 20869091 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005867</comments>
            <pubDate>Tue, 21 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005867</guid>        </item>
        <item>
            <title>[Morphological classification of glioblastomas.]</title>
            <link>http://www.medworm.com/index.php?rid=4005872&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20864138%26dopt%3DAbstract</link>
            <description>Authors: Figarella-Branger D, Bouvier C, Moroch J, Michalak S
    BACKGROUND AND PURPOSE: In the 2007 WHO classification, glioblastomas are classified among the group of astrocytic tumors. They are highly malignant (grade IV). This group of tumors is morphologically heterogeneous. The WHO distinguishes between clinico-pathological entities, variants of entities and histological pattern. Variants are defined as being reliably indentified histologically and having some relevance for clinical outcome but as still being part of a previously defined overarching entity. Patterns of differentiation are identifiable by histological appearances but without clinical or pathological significance. METHODS: The description of the histological and immunohistochemical features is based on the 2007 WHO cl...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005872</comments>
            <pubDate>Mon, 20 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4005872</guid>        </item>
        <item>
            <title>[Glioblastomas: Gliomagenesis, genetics, angiogenesis, and microenvironment.]</title>
            <link>http://www.medworm.com/index.php?rid=3955403&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20817192%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Regarding all these data, we suggest a hypothetical model of glioma initiation, growth, and progression. Moreover, the histomolecular glioma classification has been substantially revised and new therapeutic targets have been identified.
    PMID: 20817192 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3955403</comments>
            <pubDate>Wed, 01 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3955403</guid>        </item>
        <item>
            <title>Stereotactic robot-guided biospies of brain stem lesions: Experience with 15 cases.</title>
            <link>http://www.medworm.com/index.php?rid=3900455&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20728907%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: The frameless NeuroMate robot is an efficient and safe instrument for biopsies of brain stem lesions. We believe that the use of frameless stereotactic techniques for brain stem biopsies could increase the number of biopsies and therefore improve the diagnostic yield and accuracy of the technique.
    PMID: 20728907 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3900455</comments>
            <pubDate>Thu, 19 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3900455</guid>        </item>
        <item>
            <title>[Central nervous system medulloepithelioma. A report of three cases.]</title>
            <link>http://www.medworm.com/index.php?rid=3873031&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20708758%26dopt%3DAbstract</link>
            <description>We report three cases of supratentorial medulloepithelioma occurring in three children aged 11-17 years. Two patients underwent a gross-total resection followed by radiotherapy and survived more than 4 years after treatment. The third case had, however, recurred twice within the 1st postoperative month despite a complete resection each time and metastasis to the lung developed. Chemotherapy was then carried out after the third procedure and the patient died 7 months later.
    PMID: 20708758 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3873031</comments>
            <pubDate>Wed, 11 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3873031</guid>        </item>
        <item>
            <title>[Dosimetric stereotactic radiosurgical accident: Study of 33 patients treated for brain metastases.]</title>
            <link>http://www.medworm.com/index.php?rid=3873032&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20708205%26dopt%3DAbstract</link>
            <description>The objective of this study was to estimate the clinical and radiological outcome of patients treated by radiosurgery for metastasis during the period of the overexposure accident that occurred in the Toulouse Radiosurgery Unit. Between April 2006 and March 2007, 33 patients with 57 metastases were treated in the Toulouse Radiosurgery Unit (Novalis((R)), BrainLab). An initial error in the estimation of the scatter factors led to an overexposure to radiation. The median age was 55 years [range, 35-85]. Twenty-one patients (64%) harbored a single metastasis. The primary tumor location was lung (16 cases), kidney (nine cases), breast (four cases), and others (four cases). The mean tumoral volume was 3.2cm(3) [0.04-14.07]. The mean prescribed dose at the isocenter was 20 Gy [range, 10-23], the...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3873032</comments>
            <pubDate>Tue, 10 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3873032</guid>        </item>
        <item>
            <title>[Central neurocytoma: Study of 32 cases and review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=3855552&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20692674%26dopt%3DAbstract</link>
            <description>Authors: Kerkeni A, Ben Lakhdher Z, Rkhami M, Sebai R, Belguith L, Khaldi M, Ben Hamouda M
    Central neurocytoma is a rare benign neoplasm of the central nervous system. The intraventricular location close to the Monro foramina and the attachment to the septum pellucidum are characteristic for the diagnosis. However, atypical appearances may be encountered and confused with other neoplasms. The authors report the radiological findings of 32 surgically treated and pathologically confirmed neurocytomas.
    PMID: 20692674 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3855552</comments>
            <pubDate>Thu, 05 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3855552</guid>        </item>
        <item>
            <title>Intracranial meningioma in children: Different from adult forms? A series of 21 cases.</title>
            <link>http://www.medworm.com/index.php?rid=3742731&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20615516%26dopt%3DAbstract</link>
            <description>CONCLUSION: Pediatric meningiomas are larger than those found in the adult population; there is a male predominance with high incidence of a cystic component and high-grade meningiomas, thus explaining the increased recurrence rate despite the multimodal treatment.
    PMID: 20615516 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3742731</comments>
            <pubDate>Mon, 05 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3742731</guid>        </item>
        <item>
            <title>Cervical spinal extradural meningioma: Case report.</title>
            <link>http://www.medworm.com/index.php?rid=3722004&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20591451%26dopt%3DAbstract</link>
            <description>We report a case of spinal epidural meningioma diagnosed in an elderly woman complaining of right cervicobrachial pain of several years duration, associated with diffuse paresthesia and permanent numbness of her right index finger. The surgical removal of the tumor was incomplete because of the deep lateral extension of the lesion.
    PMID: 20591451 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3722004</comments>
            <pubDate>Sun, 27 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3722004</guid>        </item>
        <item>
            <title>[Recurrent giant cystic vestibular schwannomas: Role of cystoperitoneal shunt.]</title>
            <link>http://www.medworm.com/index.php?rid=3680665&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20557908%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: The cystoperitoneal shunt with no valve is a valid palliative surgical solution to remove brain stem compression. Neuronavigation allows proper positioning of the drain and secures the procedure.
    PMID: 20557908 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3680665</comments>
            <pubDate>Mon, 14 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3680665</guid>        </item>
        <item>
            <title>[Wegener granulomatosis and aneurysmal subarachnoid hemorrhage: An insignificant association?]</title>
            <link>http://www.medworm.com/index.php?rid=3556860&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20451938%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Wegener granulomatosis-related aneurysmal SAH is an exceptional condition in neurovascular pathology. As inflammatory mechanisms are involved in the pathogenesis of aneurysm, the vasculitis flare-up could account for this SAH. The management of WG could benefit from anti-inflammatory therapy, as could the vasculitis-related SAH. SAH occurrence in patients with systemic vasculitis could indicate a vasculitis flare-up.
    PMID: 20451938 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3556860</comments>
            <pubDate>Wed, 05 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3556860</guid>        </item>
        <item>
            <title>[Vertex aplasia cutis congenita with bone defect: Management synthesis and review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=3556861&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20451225%26dopt%3DAbstract</link>
            <description>We report the case of a newborn boy presenting ACC of the vertex with a skull defect. Surgical closure of the skin was performed 5 days following birth, which allowed skin healing. The skull spontaneously remodelled perfectly 6 months later. When associated with skull defect, this rare malformation characterized by the absence of skin carries the risk of severe complications such as rupture of the superior sagittal sinus or infections. Based on a review of the literature, we purpose an overview of the medical and surgical management of vertex ACC, which depends on the size of the skin defect and the presence of a skull defect.
    PMID: 20451225 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3556861</comments>
            <pubDate>Tue, 04 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3556861</guid>        </item>
        <item>
            <title>[Feasibility of auditory cortical stimulation for the treatment of tinnitus. Three case reports.]</title>
            <link>http://www.medworm.com/index.php?rid=3522881&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20427063%26dopt%3DAbstract</link>
            <description>CONCLUSION: The feasibility of cortical stimulation in symptomatic treatment of tinnitus was demonstrated by this preparatory work. The intermediate- and long-term therapeutic effects remain to be evaluated.
    PMID: 20427063 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3522881</comments>
            <pubDate>Sun, 25 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3522881</guid>        </item>
        <item>
            <title>[Imaging of orbital masses.]</title>
            <link>http://www.medworm.com/index.php?rid=3450095&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20362305%26dopt%3DAbstract</link>
            <description>Authors: H&amp;#xE9;ran F
    A wide spectrum of tumors and pseudotumors may involve the orbit. Their clinical presentation is often nonspecific, consisting of exophthalmos, diplopia, visual loss, orbital pain or signs of orbital inflammation. Imaging plays a major role in the etiological diagnosis, providing a precise analysis of the location of the lesion, its components, and its effects on adjacent and nearby structures. It studies tumor extension and often provides a good evaluation of its composition. Imaging is mainly performed with MRI. CT is needed when the lesion affects the orbital walls. Ultrasound is proposed in case of anterior location of the mass or vascular lesion. This paper presents a brief summary of the technical aspects of imaging and of the normal anatomy of the orbit and...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3450095</comments>
            <pubDate>Tue, 30 Mar 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3450095</guid>        </item>
        <item>
            <title>[Endoscopic approaches to the orbit.]</title>
            <link>http://www.medworm.com/index.php?rid=3421023&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20347457%26dopt%3DAbstract</link>
            <description>Authors: Cebula H, Lahlou A, De Battista JC, Debry C, Froelich S
    During the last decade, the use of endoscopic endonasal approaches to the pituitary has increased considerably. The endoscopic endonasal and transantral approaches offer a minimally invasive alternative to the classic transcranial or transconjunctival approaches to the medial aspect of the orbit. The medial wall of the orbit, the orbital apex, and the optic canal can be exposed through a middle meatal antrostomy, an anterior and posterior ethmoidectomy, and a sphenoidotomy. The inferomedial wall of the orbit can be also perfectly visualized through a sublabial antrostomy or an inferior meatal antrostomy. Several reports have described the use of an endoscopic approach for the resection or the biopsy of lesions located on ...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3421023</comments>
            <pubDate>Fri, 26 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3421023</guid>        </item>
        <item>
            <title>[Vascular lesions of the orbit in children.]</title>
            <link>http://www.medworm.com/index.php?rid=3421022&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20347458%26dopt%3DAbstract</link>
            <description>Authors: Dhellemmes P, Brevi&amp;#xE8;re GM, Degrugillier-Chopinet C, Vinchon M
    Vascular lesions of the orbit in children are most often hemangiomas and lymphangiomas. Hemangioma is a tumor that tends toward spontaneous regression. Lymphangioma is a malformation that tends to increase in size with growth spurts that can occur until adulthood. The treatment is decided according to the functional impact.
    PMID: 20347458 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3421022</comments>
            <pubDate>Fri, 26 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3421022</guid>        </item>
        <item>
            <title>[Orbital reconstruction in children.]</title>
            <link>http://www.medworm.com/index.php?rid=3421024&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20347103%26dopt%3DAbstract</link>
            <description>Authors: Stricker M, Simon E
    The orbital cavity, covering the globe and basement of the lids, is partially or totally impaired by tumors arising from inside or outside. In childhood, the reduction of contents jeopardizes the size of the orbit. Reconstruction is always difficult, particularly after exenteration, and a well-made prosthesis is much better than a poor reconstruction.
    PMID: 20347103 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3421024</comments>
            <pubDate>Thu, 25 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3421024</guid>        </item>
        <item>
            <title>[Preface.]</title>
            <link>http://www.medworm.com/index.php?rid=3421025&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20346472%26dopt%3DAbstract</link>
            <description>Authors: Auque J
    
    PMID: 20346472 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3421025</comments>
            <pubDate>Wed, 24 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3421025</guid>        </item>
        <item>
            <title>[Intraorbital schwannomas and solitary neurofibromas.]</title>
            <link>http://www.medworm.com/index.php?rid=3412741&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20338600%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Freppel S
    Intraorbital schwannomas and solitary neurofibromas account for 2 to 5% of all operated intraorbital tumors. Without any known neurofibromatosis, their diagnosis is only suggested with the MRI data, which displays a heterogeneous signal that may mimic a cavernous angioma. Their treatment is solely surgical.
    PMID: 20338600 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3412741</comments>
            <pubDate>Tue, 23 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3412741</guid>        </item>
        <item>
            <title>[Chronic or subacute orbital inflammation (inflammatory pseudotumors).]</title>
            <link>http://www.medworm.com/index.php?rid=3408982&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20334884%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Colnat-Coulbois S, Joud A
    Subacute or chronic orbital inflammation can cause proptosis or painful myositis. It is either primitive or secondary to systemic diseases such as polyarteritis nodosa or Wegener's granulomatosis. Corticosteroids are the basic treatment, allowing biopsy and thus anatomopathological diagnosis. Some authors advocate surgery.
    PMID: 20334884 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3408982</comments>
            <pubDate>Mon, 22 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3408982</guid>        </item>
        <item>
            <title>[Orbital tumors arising from paranasal sinuses.]</title>
            <link>http://www.medworm.com/index.php?rid=3399958&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20304444%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Pinelli C, Freppel S, Baylac F
    Orbital tumors arising from paranasal sinuses comprise mucoceles and malignant ethmoidal tumors. Most often, anamnestic, clinical, and radiological data as well as endoscopic biopsy performed by an ENT surgeon provide the preoperative diagnosis. If the tumor is benign, surgery can cure the patient. It is associated with chemotherapy and radiotherapy if the tumor is malignant.
    PMID: 20304444 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399958</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399958</guid>        </item>
        <item>
            <title>[History of orbital surgery.]</title>
            <link>http://www.medworm.com/index.php?rid=3399957&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20304445%26dopt%3DAbstract</link>
            <description>Authors: Cophignon J
    
    PMID: 20304445 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399957</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399957</guid>        </item>
        <item>
            <title>[Orbital metastasis.]</title>
            <link>http://www.medworm.com/index.php?rid=3399956&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20304446%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Colnat-Coulbois S, Freppel S
    Orbital metastases are uncommon, accounting for 4% of all adult orbital tumors. The mean age at time of presentation is 60 years. The primary tumor is most often a carcinoma involving the breast (40%), lung (11%), or prostate (8%). Proptosis is the main clinical sign at diagnosis and is often associated with visual impairment, pain or ptosis. Imaging features are not specific; nevertheless, an enhanced extraconal tumor with osteolysis suggests the diagnosis. From a pathological point of view, there are no differences between the metastasis and the primary tumor. Regarding the average survival, the gold standard treatment remains radiotherapy.
    PMID: 20304446 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399956</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399956</guid>        </item>
        <item>
            <title>[Lacrimal gland epithelial tumors.]</title>
            <link>http://www.medworm.com/index.php?rid=3399971&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303130%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Klein O, Baylac F
    Epithelial tumors of the lacrimal gland account for 50% of the expansive lesions of the lacrimal fossa. Pleomorphic adenomas have a good prognosis if surgery achieves en bloc removal distant from the tumoral capsule. Nevertheless, despite more severe treatment, the average survival remains limited for adenocarcinomas and cylindromas.
    PMID: 20303130 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399971</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399971</guid>        </item>
        <item>
            <title>[Orbitotemporal facial involvement in type 1 neurofibromatosis (NF1).]</title>
            <link>http://www.medworm.com/index.php?rid=3399970&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303131%26dopt%3DAbstract</link>
            <description>Authors: Rilliet B, Pittet B, Montandon D, Narata AP, de Ribaupierre S, Schils F, Boscherini D, Di Rocco C, Ducrey N
    Plexiform neurofibromas of the orbit, sometimes extending to the temporal region and the face, are considered to be a rare but devastating and disfiguring complication of neurofibromatosis type 1. The first symptoms appear in infancy and the involvement of the orbit and the face is present in nearly all children after the age of 5. The disease is unilateral in most cases but can exceptionally involve both sides of the face. Progressive deformation of the orbital frame due to the expanding plexiform neurofibroma and buphthalmos occurs in a large proportion of cases. The associated sphenoidal dysplasia, which is thought to be, according to the most recent hypothesis, genet...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399970</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399970</guid>        </item>
        <item>
            <title>[Descriptive anatomy of the orbit.]</title>
            <link>http://www.medworm.com/index.php?rid=3399969&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303548%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Froelich S, Joud A, Perez M, Mercier P
    Anatomical description of the orbit is essential for an accurate understanding of its related tumoral pathologies. Numerous cadaveric pictures illustrate this chapter, which contains the description of the bony walls of the orbit and its muscular nerve, and vascular structures.
    PMID: 20303548 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399969</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399969</guid>        </item>
        <item>
            <title>[Conclusion.]</title>
            <link>http://www.medworm.com/index.php?rid=3399968&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303549%26dopt%3DAbstract</link>
            <description>Conclusion.]
    Neurochirurgie. 2010 Mar 18;
    Authors: Civit T
    
    PMID: 20303549 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399968</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399968</guid>        </item>
        <item>
            <title>[Malignant extraconal tumors of the orbit in childhood.]</title>
            <link>http://www.medworm.com/index.php?rid=3399967&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303550%26dopt%3DAbstract</link>
            <description>Authors: Chastagner P
    Malignant extraconal orbital tumors are very rare during childhood and must be referred as soon as possible to a highly specialized center to be managed by a multidisciplinary team. They are often referred on an emergency basis. Both diagnosis and treatment must be undertaken as soon as possible. The course of these malignant tumors can be acute and can jeopardize the function of the eye or be life-threatening, especially in the event of metastatic locations. Extra-axial proptosis is by far the most frequent revealing symptom. Local and general examinations are of utmost importance. Sometimes diagnosis should be clear with the association of an orbital tumor and deterioration of the general health status favoring metastatic disease. Most metastatic neuroblastomas ...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399967</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399967</guid>        </item>
        <item>
            <title>[Congenital orbital tumors in adults (dermoid cysts).]</title>
            <link>http://www.medworm.com/index.php?rid=3399966&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303551%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Joud A, Klein O
    The most frequent intraorbital congenital tumors are dermoid cysts, which account for 2-9% of all orbital tumors. Teratomas are also congenital tumors but occur only in children. The revealing clinical sign is a subcutaneous mass along the superior orbital rim if the cyst is superficial or proptosis if the cyst is deep. Neuroradiological work-up provides the preoperative diagnosis. The treatment is solely surgical.
    PMID: 20303551 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399966</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399966</guid>        </item>
        <item>
            <title>[Primary bone tumors of the orbit.]</title>
            <link>http://www.medworm.com/index.php?rid=3399965&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303552%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Freppel S, Baylac F
    Primary orbital bone tumors account for 0.6-2% of all orbital tumors. This is a heterogeneous group of tumors arising from osseous, cartilaginous, fibrous, and vascular tissues. The two most commonly encountered lesions are fibrous dysplasia and osteoma. Treatment of the primitive orbital bone tumors is generally surgical.
    PMID: 20303552 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399965</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399965</guid>        </item>
        <item>
            <title>[Optic nerve glioma in children.]</title>
            <link>http://www.medworm.com/index.php?rid=3399964&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303553%26dopt%3DAbstract</link>
            <description>Authors: Lena G, Pech-Gourg G, Scavarda D, Klein O, Paz-Paredes A
    Optic pathway gliomas are rare tumors accounting for 3-5% of brain tumors in children; 90% are observed in children. They account for 4% of orbital tumors in children. Association with NF 1 is classical and the incidence of NF 1 in patients with optic pathway gliomas is estimated at 30-58%. Usually these tumors are pilocytic astrocytomas and their regression, particularly in patients with NF 1, has been described. Exophthalmos and loss of visual acuity or blindness are the usualpresentation in progressive disease. CT and above all MRI study of the orbit and the brain are necessary to make a complete evaluation of the disease. Gross total removal of the tumor provides 100% cure, but surgery can be proposed only for growin...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399964</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399964</guid>        </item>
        <item>
            <title>[Vascular tumors of the orbit.]</title>
            <link>http://www.medworm.com/index.php?rid=3399963&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303554%26dopt%3DAbstract</link>
            <description>Authors: Cophignon J, d'Hermies F, Civit T
    Vascular tumors of the orbit include capillary hemangioma, cavernous hemangioma, hemolymphangioma, hemangiopericytoma and a few rare tumors. Capillary hemangioma and hemolymphangioma, occurring mainly in children, are covered in the chapter devoted to childhood tumors. In this chapter, cavernous hemangioma and hemangiopericytoma are discussed as well as rare vascular tumors. Although orbital varix is not a tumor, it is also considered because of the diagnostic problems and the close correlation of orbital varix with a true tumor: hemolymphangioma.
    PMID: 20303554 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399963</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399963</guid>        </item>
        <item>
            <title>[Orbital tumors in children: Clinical examination, imaging, specific progression.]</title>
            <link>http://www.medworm.com/index.php?rid=3399962&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303555%26dopt%3DAbstract</link>
            <description>Authors: George JL, Marchal JC
    &quot;Orbital tumors (OT) are neoplasms of the bony orbit and contents except for the eyeball.&quot; Given this definition, we exclude the retinoblastomas, which are the most frequent tumors of this anatomical area in the pediatric population. Although these tumors are rare, there is a great variety of etiologies. Among them, the most frequent OTs in childhood are rhabdomyosarcomas and metastatic tumors: metastatic neuroblastomas and leukemias (chloromas). Moreover, adult and pediatric varieties of OT are made up of two clusters of distinctive histological entities. Examination must be careful: measurement, direction of proptosis, impairment of ocular motility, compressive optic neuropathy, strabismus, etc. Age at onset as well as unilateral or bilateral proptosis ...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399962</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399962</guid>        </item>
        <item>
            <title>[Neurosurgical approaches to the orbit.]</title>
            <link>http://www.medworm.com/index.php?rid=3399961&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303556%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Cophignon J
    Surgical approaches to the orbit differ depending on the surgical specialty. Neurosurgical approaches consider the posterior two-thirds of the orbit and can be summed up as the superior, lateral, and superolateral approaches. Orbital rim removal enlarges the exposure when necessary. Each neurosurgical approach is described in this chapter. Schematically, subfrontal approaches are used to reach the inner quadrant orbital tumors and the others to access external quadrant tumors. Nevertheless, the choice of the approach is discussed regarding to the presumed pathologic preoperative diagnosis.
    PMID: 20303556 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399961</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399961</guid>        </item>
        <item>
            <title>[Sphenoorbital meningiomas.]</title>
            <link>http://www.medworm.com/index.php?rid=3399960&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303557%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Freppel S
    Sphenoorbital meningiomas account for 20% of all orbital tumors treated by neurosurgeons. Proptosis is the main clinical sign but this can be reduced with accurate surgical management. Complete tumor removal is often difficult considering the frequent extensions of the meningioma to the superior orbital fissure, the cavernous sinus, and the periorbita.
    PMID: 20303557 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399960</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399960</guid>        </item>
        <item>
            <title>[Orbital tumors: The ophthalmologist's point of view (biopsies - approaches - exenteration).]</title>
            <link>http://www.medworm.com/index.php?rid=3399959&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20303558%26dopt%3DAbstract</link>
            <description>Authors: George JL
    This publication details the indications and contraindications of orbital tumor biopsies and surgical removal. Until now biopsies of pleomorphic adenomas were contraindicated. This management is now being reconsidered. Contrary to past convention, for suspected malignant tumors, a biopsy is essential. Great caution is required in surgery of inflammatory pseudotumors. Surgery is not recommended in lymphomas.
    PMID: 20303558 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3399959</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3399959</guid>        </item>
        <item>
            <title>[Hematopoietic orbital tumors.]</title>
            <link>http://www.medworm.com/index.php?rid=3386228&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20299065%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Colnat-Coulbois S, Joud A
    Non Hodgkin B cell lymphomas account for most hematopoietic orbital tumors and 10 % of all orbital tumors. Typically, orbital lymphomas present as salmon-pink, painless, and slow growing conjunctival tumors affecting patients over 50 years of age. Therapeutic orientation is guided by biopsy.
    PMID: 20299065 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3386228</comments>
            <pubDate>Tue, 16 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3386228</guid>        </item>
        <item>
            <title>[Orbital tumors. Neurosurgical activity.]</title>
            <link>http://www.medworm.com/index.php?rid=3386227&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20299066%26dopt%3DAbstract</link>
            <description>Authors: Bousquet O, El Ouahabi A, Le Reste PJ, Sacko O, Joud A, Hayek G, Froelich S, Mourier KL, Mercier P, Vignes JR, Loiseau H, Liguoro D, Scherpereel B, Rousseaux P, Gay E, Brassier G, Laguarrigue J, Cophignon J, Civit T
    In this chapter, we report the results of orbital tumor management in a few neurosurgical departments and compare it to a Paris neurosurgical department that has developed a close relation with an ophthalmological department. These departments' activity is quite low, treating mainly sphenoorbital meningiomas. Other tumor groups are unequally and sporadically managed.
    PMID: 20299066 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3386227</comments>
            <pubDate>Tue, 16 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3386227</guid>        </item>
        <item>
            <title>[Optic nerve sheath meningiomas.]</title>
            <link>http://www.medworm.com/index.php?rid=3374468&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20227092%26dopt%3DAbstract</link>
            <description>Authors: Litre CF, Colin P, Rousseaux P, Civit T
    Optic nerve sheath meningiomas account for one-third of optic nerve tumors, 1-2 % of all meningiomas, and 2-3.5 % of all orbital tumors. Loss of vision is the main clinical sign. Diagnosis is easily made after the neuroradiological evaluation. Fractionated stereotactic radiotherapy (RSF) is now the gold standard treatment for controlling tumor volume and preserving visual acuity.
    PMID: 20227092 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3374468</comments>
            <pubDate>Thu, 11 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3374468</guid>        </item>
        <item>
            <title>[Mesenchymal orbital tumors.]</title>
            <link>http://www.medworm.com/index.php?rid=3374467&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20227093%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Klein O, Freppel S, Baylac F
    Mesenchymal tumors grow from pluripotent mesenchymal cells that form the soft orbital tissue. Primary tumors of the orbital walls are discussed in another section. Tumors from muscle and adipose tissue are rare or exceptional, except rhabdomyosarcoma, described in the section dedicated to pediatric tumors. Most frequent tumors are fibrous histiocytomas and solitary fibrous tumors, which often have a retrobulbar location. Fibrous histiocytoma is benign in only 65 % of cases. Fibrous solitary tumor is now better known (Ag CD34): this tumor is generally benign but frequently recurs.
    PMID: 20227093 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3374467</comments>
            <pubDate>Thu, 11 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3374467</guid>        </item>
        <item>
            <title>[Classification of orbital tumors.]</title>
            <link>http://www.medworm.com/index.php?rid=3374466&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20227094%26dopt%3DAbstract</link>
            <description>Authors: Civit T
    Knowledge of orbital tumor classification is essential because it is the basis of an optimal therapeutic strategy. These tumors comprise the sphenoorbital meningiomas, the optic nerve sheath meningiomas, the optic nerve gliomas, the schwannomas, the histiocytic tumors, the metastases, the lacrimal gland tumors, the mesenchymal tumors of the soft tissues, the primary orbital wall tumors, the tumors arising from the nasal and paranasal sinuses, the hematopoietic tumors, the vascular tumors, and the congenital tumors.
    PMID: 20227094 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3374466</comments>
            <pubDate>Thu, 11 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3374466</guid>        </item>
        <item>
            <title>[Orbital tumours in children. Introduction.]</title>
            <link>http://www.medworm.com/index.php?rid=3374471&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20226482%26dopt%3DAbstract</link>
            <description>Authors: Marchal JC, Klein O
    
    PMID: 20226482 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3374471</comments>
            <pubDate>Wed, 10 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3374471</guid>        </item>
        <item>
            <title>[Introduction.]</title>
            <link>http://www.medworm.com/index.php?rid=3374470&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20226483%26dopt%3DAbstract</link>
            <description>Authors: Civit T
    
    PMID: 20226483 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3374470</comments>
            <pubDate>Wed, 10 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3374470</guid>        </item>
        <item>
            <title>[Histiocytic disorders with orbital involvement.]</title>
            <link>http://www.medworm.com/index.php?rid=3374469&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20226484%26dopt%3DAbstract</link>
            <description>Authors: Civit T, Colnat-Coulbois S, Marie B
    The eosinophilic granuloma of bone is the most common type of histiocytic disorder involving the orbital area. Imaging data typically show bony defects with an intra-orbital soft-tissue extension. Surgical debulking is most often required. Rosai-Dorfman disease is commonly associated with uni- or bilateral orbital locations. The other histiocytic disorders are very rare, but some have a poor prognosis such as Erdheim-Chester disease.
    PMID: 20226484 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3374469</comments>
            <pubDate>Wed, 10 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3374469</guid>        </item>
        <item>
            <title>[Foreword.]</title>
            <link>http://www.medworm.com/index.php?rid=3255389&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20138638%26dopt%3DAbstract</link>
            <description>Authors: Fransen P
    
    PMID: 20138638 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3255389</comments>
            <pubDate>Fri, 05 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3255389</guid>        </item>
        <item>
            <title>[Posterior fossa extradural and extracranial hydatid cyst.]</title>
            <link>http://www.medworm.com/index.php?rid=3255390&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20138319%26dopt%3DAbstract</link>
            <description>We report the case of a 37-year-old admitted for high intracranial pressure. Brain MRI showed an extradural and extracranial posterior fossa cyst without enhancement after contrast medium injection. Multiple hydatid cysts were removed and the histological examination of the tissue sample confirmed the diagnosis. The patient was given albendazole postoperatively with good follow-up 6 months later.
    PMID: 20138319 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3255390</comments>
            <pubDate>Thu, 04 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3255390</guid>        </item>
        <item>
            <title>[Surgical treatment of cerebellar infarction: Five case studies.]</title>
            <link>http://www.medworm.com/index.php?rid=3231851&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20116075%26dopt%3DAbstract</link>
            <description>CONCLUSION: These results suggest that decompressive suboccipital craniotomy may be an effective solution for good recovery if the patient is operated early, at the moment of the neurological deterioration.
    PMID: 20116075 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3231851</comments>
            <pubDate>Wed, 27 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3231851</guid>        </item>
        <item>
            <title>[Minimally invasive spine arthrodesis in degenerative spinal disorders.]</title>
            <link>http://www.medworm.com/index.php?rid=3231850&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20116076%26dopt%3DAbstract</link>
            <description>This article reviews the value of these approaches in the treatment of degenerative lumbar spine disorders. METHODS: We describe the main techniques used in minimally invasive lumbar spine surgery, including posterior pedicle screwing as well as anterior (ALIF), posterior (PLIF), transforaminal (TLIF), extreme lateral (XLIf), and presacral (AxiaLIF) interbody fusion. The results of recently published series are reported. RESULTS: Percutaneous pedicle screwing is reported to be an effective technique of lumbar spine arthrodesis associated with a low rate of screw misplacement. Minimally invasive PLIF, TLIF, and ALIF have been associated with shorter mean operative time, less postoperative pain, reduction of the estimated blood loss, a shorter hospital stay, and quicker functional recovery. ...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3231850</comments>
            <pubDate>Wed, 27 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3231850</guid>        </item>
        <item>
            <title>[Intramedullary tumors. Results of a national investigation in private neurosurgery.]</title>
            <link>http://www.medworm.com/index.php?rid=3213197&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20097390%26dopt%3DAbstract</link>
            <description>CONCLUSION: Total removal of the intramedullary tumors is a challenge. In cases of removal, the risk of worsening status is 18-19.5%. Subtotal or incomplete removal 27-40% risk of recurrence.
    PMID: 20097390 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3213197</comments>
            <pubDate>Fri, 22 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3213197</guid>        </item>
        <item>
            <title>[Contribution of phase-contrast MRI to the management of patients with normal pressure hydrocephalus: Can it predict response to shunting?]</title>
            <link>http://www.medworm.com/index.php?rid=3213196&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20097391%26dopt%3DAbstract</link>
            <description>The objective of this study was to investigate whether cerebrospinal fluid (CSF) flow dynamics is linked to post-shunt improvement. Fourteen NPH patients (nine males and five females; mean age, 68 years) investigated by magnetic resonance imaging (MRI) before surgical diversion of CSF were retrospectively reviewed. Phase-contrast sequences were added to the morphological clinical protocol for quantification of CSF oscillations, which were recorded at the level of the cerebral aqueduct and the C2 and C3 subarachnoid spaces (SAS). The phase-contrast images were analysed with custom-designed dedicated flow segmentation software. The oscillations measured in this hydrocephalus population were compared to a previously studied healthy population. A difference of at least two standard deviations ...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3213196</comments>
            <pubDate>Fri, 22 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3213196</guid>        </item>
        <item>
            <title>[Ventriculus terminalis dilatation in adults: A case report and review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=3213195&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20097392%26dopt%3DAbstract</link>
            <description>We present the case of a 47-year-old woman who presented with hypoesthesia and dysesthesia of the lower limb, distal paresis, and urinary dysfunction evolving for the past 5years. Electrophysiology confirmed radiculopathy. MRI revealed a cystic dilatation of the VT. Surgery consisted in laminectomy with myelotomy and fenestration. Histology showed a simple cubic ependymal epithelium. Progression has been favorable concerning the motor deficit and sphincter dysfunction but neuropathic pain has persisted for 6months. The data are similar to those found in the literature. The sex ratio is 6:21, the mean age is 45. Symptoms appear on average over 2years with lower limb pain (71 %), sphincter dysfunction (71 %), lumbago (64 %), motor deficits (57 %), and sensory disorders (47 %). Imaging demons...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3213195</comments>
            <pubDate>Fri, 22 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3213195</guid>        </item>
        <item>
            <title>[History of pituitary surgery.]</title>
            <link>http://www.medworm.com/index.php?rid=3213199&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20096901%26dopt%3DAbstract</link>
            <description>Authors: Hardy J
    Over the last few decades, the scientific literature has acquired over 100 publications on pituitary surgery. Most of these papers contain a brief historical review of the work of the pioneers who contributed to operative modalities (Landolt et al., 1996; Liu et al., 2001; Walker, 1951; Welbourne, 1986). Several have been only experimental explorations on cadavers, used on a few patients, but were eventually abandoned, retaining only anecdotal value. In fact, open surgery currently uses the two classical approaches: intracranial and extracranial. The superior transcranial approach has retained two modalities: (1) subfrontal basal with or without resection of the orbital ridge and (2) subfrontal or subfrontotemporal. The inferior trans-sphenoidal approach currently main...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3213199</comments>
            <pubDate>Thu, 21 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3213199</guid>        </item>
        <item>
            <title>[Vertebroplasty and balloon kyphoplasty.]</title>
            <link>http://www.medworm.com/index.php?rid=3213198&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20096902%26dopt%3DAbstract</link>
            <description>Authors: Fuentes S, Blondel B
    Since the first report more than 20 years ago, vertebroplasty is now performed as a routine procedure by radiologists. The main goal of this technique is to fill the fractured vertebral body with PMMA cement to improve its stability. The efficiency of vertebroplasty on spinal pain related to osteoporotic fractures or the tumorous process has been widely described in the literature. However, the main problem of this percutaneous approach is the risk of cement leakage; to avoid this danger, balloon kyphoplasty was developed. There are two main goals of using balloons: first to reduce the deformity of the fractured vertebral body by inflation and then to fill the cavity created with cement injected without pressure. During the last 8 years kyphoplasty has bee...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3213198</comments>
            <pubDate>Thu, 21 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3213198</guid>        </item>
        <item>
            <title>Non-traumatic pseudocyst of Glisson capsule complicating a ventriculoperitoneal shunt.</title>
            <link>http://www.medworm.com/index.php?rid=3213201&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20096426%26dopt%3DAbstract</link>
            <description>CONCLUSION: Reinsertion of the catheter at a different abdominal site is effective in non-infections cases. In contrast, a temporary external drainage with adequate antibiotic treatment followed by shunt reinsertion is necessary to treat a documented infection of CSF collections.
    PMID: 20096426 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3213201</comments>
            <pubDate>Wed, 20 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3213201</guid>        </item>
        <item>
            <title>[Apoplectic macroadenomas: The outcome of the residual pituitary gland.]</title>
            <link>http://www.medworm.com/index.php?rid=3213200&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20096427%26dopt%3DAbstract</link>
            <description>CONCLUSION: The repercussions of adenomatous apoplexy on the RPG is significant: only 27 % of the patients retained normal pituitary function. Furthermore, although the RPG was identified on the MRI in more than two-thirds of the cases, more than half had adenohypophyseal failure: therefore, the visualization of a RPG does not mean that its functions are preserved. The involvement of the neurohypophysis is much rarer: one patient of 19 (5 %). The implications of the ischemic or compressive damage on the normal pituitary gland are discussed.
    PMID: 20096427 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3213200</comments>
            <pubDate>Wed, 20 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3213200</guid>        </item>
        <item>
            <title>[Treatment of grade 0 intracranial aneurysms: Retrospective study of 79 cases.]</title>
            <link>http://www.medworm.com/index.php?rid=3188076&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20083285%26dopt%3DAbstract</link>
            <description>DISCUSSION: Many factors are involved in the therapeutic decision: UIA location and size and individual risks. Progress in both surgery and interventional neuroradiology has led to good results conforming with the data reported in the literature but does not demonstrate the superiority of one technique over another.
    PMID: 20083285 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3188076</comments>
            <pubDate>Sat, 16 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3188076</guid>        </item>
        <item>
            <title>[Spinal cord compression caused by idiopathic dorsal epidural lipomatosis: Case report and critical review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=3179206&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20074758%26dopt%3DAbstract</link>
            <description>We report the case of a patient with spinal cord compression evolving over 36 months with spastic paraparesis. Anatomic imagery showed epidural lipomatosis. No predisposing factors were found. Surgical treatment was decided. A T1-T10 laminectomy with excision of the surplus epidural fat was performed. Immediate and medium-term postsurgical follow-up was favorable with the disappearance of the pyramidal syndrome. Other cases found in literature and the principal predisposing factors are discussed.
    PMID: 20074758 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3179206</comments>
            <pubDate>Tue, 12 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3179206</guid>        </item>
        <item>
            <title>[MRI sequences for detection of neurovascular conflicts in patients with trigeminal neuralgia and predictive value for characterization of the conflict (particularly degree of vascular compression).]</title>
            <link>http://www.medworm.com/index.php?rid=3164564&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20060548%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: High-resolution 3D T2-weighted imaging in combination with angio-MR-TOF is a reliable technique for detecting NVC and predicting the degree of the compression in NVC.
    PMID: 20060548 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3164564</comments>
            <pubDate>Thu, 07 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3164564</guid>        </item>
        <item>
            <title>[Aneurismal subarachnoid hemorrhage in the elderly subject. Should this patient participate in a randomized clinical trial?]</title>
            <link>http://www.medworm.com/index.php?rid=3164563&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20060549%26dopt%3DAbstract</link>
            <description>Authors: Proust F, Bracard S, Thines L, Leclerc X, Penchet G, Berg&amp;#xE9; J, Vignes JR, Irthum B, Gabrillargues J, Chazal J, Bataille B, Drouinau J, Mourier K, Ricolfi F, Gay E, Bessou P, Lonjon M, Sedat J, David P, Lajaunias P, Morandi X, Gauvrit JY, Pelissou I, Turjman F, Roche PH, Dufour H, Levrier O, Emery E, Courth&amp;#xE9;oux P, Laguarrigue J, Cognard C, Civit T, Lejeune JP
    
    PMID: 20060549 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3164563</comments>
            <pubDate>Thu, 07 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3164563</guid>        </item>
        <item>
            <title>[Minimally invasive surgery for Chance fractures: Three case studies.]</title>
            <link>http://www.medworm.com/index.php?rid=3142995&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20045158%26dopt%3DAbstract</link>
            <description>CONCLUSION: Percutaneous osteosynthesis and minimally invasive surgery can be an advantageous alternative for the management of Chance fractures. They allow early mobilization of the patient with less soft tissue trauma and morbidities associated with open procedures.
    PMID: 20045158 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3142995</comments>
            <pubDate>Wed, 30 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3142995</guid>        </item>
        <item>
            <title>[Second surgery for glioblastoma. A 4-year retrospective study conducted in both the Montpellier and Nice Departments of Neurosurgery. A literature review.]</title>
            <link>http://www.medworm.com/index.php?rid=3142994&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20045159%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: The effect of resection of recurrent glioblastoma on survival has not been extensively studied. No randomized trials have been conducted. Our data were globally identical to other retrospective studies. Selected patients with recurrent glioblastoma may be candidates for repeated surgery when the situation appears favorable based on assessment of the individual patient's factors. Factors such medical history, neurological status, location of the tumor, and progression-free survival have been proven in retrospective studies to give better results.
    PMID: 20045159 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3142994</comments>
            <pubDate>Wed, 30 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3142994</guid>        </item>
        <item>
            <title>Hemangioblastoma of the corpus callosum: A case report and review of the literature on its origin.</title>
            <link>http://www.medworm.com/index.php?rid=3142993&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20045160%26dopt%3DAbstract</link>
            <description>Authors: Sacko O, Bouillot-Eimer S, Sesay M, Uro-Coste E, Roux FE, Loiseau H
    A third case of corpus callosum hemangioblastoma (HB) is presented. With no preoperative embolization, surgery was uneventful and the postoperative course was excellent. Based on the literature, we attempted to clarify the histogenesis of HB and to explain why they are exceptional in the supratentorial region in contrast to the posterior cranial fossa. The VHL gene is expressed particularly in Purkinje cells of the cerebellum, but this expression is also possible in supratentorial structures. Its mutation leads to developmental arrest of angioblasts that become potentially neoplastic cells. These CD133-positive pluripotent neoplastic angioblasts, similar to stem cells, may be immature HB in the brain. They als...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3142993</comments>
            <pubDate>Wed, 30 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3142993</guid>        </item>
        <item>
            <title>[Contribution of neuroradiology to the evaluation of peripheral nerves.]</title>
            <link>http://www.medworm.com/index.php?rid=2879425&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19811793%26dopt%3DAbstract</link>
            <description>Authors: Chan M, Pesquer L, Vandermarcq P
    The evaluation of peripheral nerve impairment can use echography, MRI and CT. The alteration of the nerves in tunnel syndromes, especially if symptoms are not sufficiently contributive, is clearly visualized with MRI. Echography is very useful in the diagnosis of nerve tumors and neuromas. Plexus brachial palsies need to be evaluated using MRI. Progress in neuroimaging has improved clinical practice so that the most relevant treatment can be chosen for some pathologies such as infiltration performed under CT scanner guidance. The authors report which exam to use and the results to be expected for each pathology.
    PMID: 19811793 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2879425</comments>
            <pubDate>Sun, 04 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2879425</guid>        </item>
        <item>
            <title>[Anatomic bases of surgical approaches to the nerves of the lower limb: Tips for young surgeons.]</title>
            <link>http://www.medworm.com/index.php?rid=2866091&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19800088%26dopt%3DAbstract</link>
            <description>Authors: Rigoard P, Buffenoir-Billet K, Giot JP, d'Houtaud S, Delmotte A, Lapierre F
    For trainee surgeons, the surgical approaches of the lower limb's peripheral nerves remain partially or completely unknown, but traumatic nerve lesions are rather frequent at this level and nerve tumors require intervention. Young surgeons will also have to treat spasticity and perform selective neurotomies, which can provide dramatic improvement of the functional status of properly selected patients. Excellent knowledge of anatomy is the key point to successful surgery. For each nerve approach, the key points on the morphological data of the nerve and its surroundings are given, as are the typical indications for this surgery and certain particularities related to patient installation in the operating...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2866091</comments>
            <pubDate>Wed, 30 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2866091</guid>        </item>
        <item>
            <title>[Thoracic outlet syndromes.]</title>
            <link>http://www.medworm.com/index.php?rid=2866090&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19800643%26dopt%3DAbstract</link>
            <description>Authors: Gilbert A
    Thoracic outlet syndromes (TOS) may induce neurologic signs, vascular pathology, and pain, but the clinical signs are often unclear. The relationship between a cervical bony abnormality is often unclear, and the investigations not always contributive. First-line treatment consists in physiotherapy. Surgery remains controversial, in both its indication as its modalities. However, well-adapted surgery gives a good result in 60-85% of cases.
    PMID: 19800643 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2866090</comments>
            <pubDate>Wed, 30 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2866090</guid>        </item>
        <item>
            <title>---</title>
            <link>http://www.medworm.com/index.php?rid=2866093&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19800086%26dopt%3DAbstract</link>
            <description>Neurochirurgie. 2009 Sep 30;
    Authors: Lapierre F
    
    PMID: 19800086 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2866093</comments>
            <pubDate>Tue, 29 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2866093</guid>        </item>
        <item>
            <title>[The main tunnel syndromes.]</title>
            <link>http://www.medworm.com/index.php?rid=2866092&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19800087%26dopt%3DAbstract</link>
            <description>Authors: Lapierre F, Buffenoir K, Giot JP, Delmotte A, Rigoard P
    Several tunnel syndromes are responsible for substantial functional impairment. The diagnosis has to be made and treatment is most often very simple - nerve decompression - with excellent results. Of these syndromes, the most common are median and ulnar tunnel syndromes of the wrist and ulnar tunnel syndrome of the elbow, but other syndromes must be identified at the risk of therapy failure due to poorly adapted treatment. Finally, good knowledge of this pathology must lead to prevention of the iatrogenic forms (sequelae of inguinal hernia treatment, ileac crest graft harvesting) by educating all surgeons interested in peripheral nerve surgery.
    PMID: 19800087 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgi...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2866092</comments>
            <pubDate>Tue, 29 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2866092</guid>        </item>
        <item>
            <title>[Peripheral nerve tumors.]</title>
            <link>http://www.medworm.com/index.php?rid=2859277&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19796780%26dopt%3DAbstract</link>
            <description>Authors: Lapierre F, Rigoard P, Wager M
    Peripheral nerve tumors are most often benign tumors of the nerve sheath; uncommonly they come from the nerve cells or are metastatic tumors. A precise diagnosis is required for well-adapted and effective treatment, as is good knowledge of fibromatosis diseases. In some cases, the diagnosis of the nerve tumor will lead to a diagnosis of phakomatosis. Surgical treatment must be clearly discussed, which, in case of schwannomas gives very good functional results. Primitive malignant tumors remain an unsolved therapeutic problem.
    PMID: 19796780 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2859277</comments>
            <pubDate>Mon, 28 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2859277</guid>        </item>
        <item>
            <title>[Management and results of treating obstetrical palsy in the new-born.]</title>
            <link>http://www.medworm.com/index.php?rid=2856205&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19793598%26dopt%3DAbstract</link>
            <description>Authors: Gilbert A
    Birth injuries to the brachial plexus have not disappeared in spite of improvements in obstetrics. Many of these palsies spontaneously recover but some will require a surgical approach. Over the last 30 years, the author has explored and repaired 1026 brachial plexus injuries in infants who had not recovered biceps function after three months. Repair is always feasible and its results far better than spontaneous progression. The results are evaluated after 20 years of follow-up for some patients. Their evaluation confirms the importance of early plexus surgery.
    PMID: 19793598 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2856205</comments>
            <pubDate>Sun, 27 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2856205</guid>        </item>
        <item>
            <title>[Peripheral nerve surgery in leprosy.]</title>
            <link>http://www.medworm.com/index.php?rid=2856204&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19793599%26dopt%3DAbstract</link>
            <description>Authors: Redondo A
    Leprosy has nearly disappeared in France but continues to affect two million patients in the world. Involvement of the peripheral nerve must be identified and requires surgical treatment, which can provide good results for pain and function. The author reviews the most frequently affected peripheral nerves and reports her personal series, with surgery performed concomitantly with the medical treatment of the disease.
    PMID: 19793599 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2856204</comments>
            <pubDate>Sun, 27 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2856204</guid>        </item>
        <item>
            <title>[Anatomic bases of surgical approaches to the nerves of the upper limb: Tips for young surgeons.]</title>
            <link>http://www.medworm.com/index.php?rid=2839533&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19783016%26dopt%3DAbstract</link>
            <description>Authors: Rigoard P, Buffenoir-Billet K, Giot JP, Delmotte A, d'houtaud S, Lapierre F
    Peripheral nerve surgery requires a certain level of specialization. Surgeons must have solid knowledge of morphological anatomy of the different segments to be explored, decompressed, repaired, or even neurotized. This paper describes the most common approaches to the peripheral nerves of the upper limb.
    PMID: 19783016 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2839533</comments>
            <pubDate>Thu, 24 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2839533</guid>        </item>
        <item>
            <title>[Review of the peripheral nerve.]</title>
            <link>http://www.medworm.com/index.php?rid=2839532&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19783017%26dopt%3DAbstract</link>
            <description>Authors: Rigoard P, Lapierre F
    The peripheral nerve provides the pathway for motor, sensory, and vegetative axons belonging to the peripheral nervous system. It transmits information between these neurons and their peripheral effectors in both directions (sensory receptors, skeletal muscles, and viscera). The afferences to the periphery correspond to the nerve motor content, whereas efferences from the periphery, in charge of delivering information to the central integrators, correspond to nerve-sensitive content. This information support depends on the intrinsic properties of the nerve itself. Peripheral nerve injuries are frequent and generate significant deficits. Their treatment sometimes leads to functional recovery but is mostly incomplete or unpredictable, despite the regular us...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2839532</comments>
            <pubDate>Thu, 24 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2839532</guid>        </item>
        <item>
            <title>[The pudendal nerve: Clinical and therapeutic morphogenesis, anatomy, and physiopathology.]</title>
            <link>http://www.medworm.com/index.php?rid=2798026&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19748642%26dopt%3DAbstract</link>
            <description>Authors: Robert R, Labat JJ, Riant T, Louppe JM, Hamel O
    The pudendal is the king of the perineum. Most often originating in the S3 root, it is responsible for the teguments of the perineum (glans penis, clitoris, scrotum, and the labia majora, the skin of the central fibrous perineal body, anus), but also the erector muscles and the striated sphincters. The social nerve, it controls erection and the voluntary sphincters. It is also the nerve of the beginnings of sexual sensation and masturbation. Its injury is expressed in perineal pain, which, when positional, suggests a tunnel syndrome. The compression points have become well known: ligament pinching between the sacrotuberous and sacrospinous ligaments, the falciform process and the pudendal canal (Alcock canal). The data from quest...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2798026</comments>
            <pubDate>Thu, 10 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2798026</guid>        </item>
        <item>
            <title>[Electrophysiological exploration of tunnel syndromes.]</title>
            <link>http://www.medworm.com/index.php?rid=2798027&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19748105%26dopt%3DAbstract</link>
            <description>Authors: Dumas P
    The compressive neuropathies often lead to segmental demyelination injury. These injuries can be detected using speed motor conduction and sensitivity conduction. The corresponding abnormalities are localized conduction abnormalities, presenting as deceleration or as a conductive block. Segmentary deceleration is perfectly well observed, such as in cases of carpal tunnel syndrome. The detection examination, recording motor unit potentials, can distinguish between a peripheral injury and a central injury as well as between a neurogenic injury and a myogenous injury. The precise study of the sensitivity potentials makes it possible to distinguish between a radicular injury, in which the sensitivity potentials are normal, and a plexus injury, in which the sensitivity pote...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2798027</comments>
            <pubDate>Wed, 09 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2798027</guid>        </item>
        <item>
            <title>[Somatic perineal pain other than pudendal neuralgia.]</title>
            <link>http://www.medworm.com/index.php?rid=2789335&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19744676%26dopt%3DAbstract</link>
            <description>Authors: Robert R, Labat JJ, Riant T, Louppe JM, Lucas O, Hamel O
    In addition to the well-established syndrome of pudendal compression, and given the rich nerve trunk innervation of the perineum, pain originating in other nerve trunks can occur and must be remembered. Nerves originating high in the thoracolumbar area (ilioinguinal nerve, iliohypogastric nerve, genitor femoral nerve) can be the seat of traumatic lesions occurring during surgical approaches through the abdominal wall or can undergo compressions when crossing the fascia of the large abdominal muscles. Misleading perineal irradiations do not resemble pudendal neuralgia and should suggest pain in these trunks whose cutaneous territories are not solely perineal and whose clinical expression as pain is does not occur in the s...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2789335</comments>
            <pubDate>Mon, 07 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2789335</guid>        </item>
        <item>
            <title>[Pathologic characteristics of the most frequent peripheral nerve tumors.]</title>
            <link>http://www.medworm.com/index.php?rid=2789334&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19744677%26dopt%3DAbstract</link>
            <description>Authors: Coulon A, Milin S, Laban E, Debiais C, Jamet C, Goujon JM
    Benign tumors of the peripheral nerves come from ectodermic tissues. This chapter describes the most common forms: the schwannomas and the neurofibromas. Schwannomas have two possible patterns of cells: Antoni A and B types. Neurofibromas are most often associated with neurofibromatosis NF(1) and may be localized, diffuse, or plexiform. The benign tumor structures account for the fact that they can be removed with or without preserving the concerned nerve. Malignant tumors (malignant peripheral sheath tumors) come from degeneration of neurofibromas in two out of three cases and have a poor prognosis.
    PMID: 19744677 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2789334</comments>
            <pubDate>Mon, 07 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2789334</guid>        </item>
        <item>
            <title>[Buttocks sciatic pain.]</title>
            <link>http://www.medworm.com/index.php?rid=2789333&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19744678%26dopt%3DAbstract</link>
            <description>Authors: Labat JJ, Robert R, Riant T, Louppe JM, Lucas O, Hamel O
    Confusion between radicular and nerve trunk syndrome is not rare. With sciatic pain, any nerve trunk pain or an atypical nerve course should suggest nerve trunk pain of the sciatic nerve in the buttocks. The usual reflex with sciatic pain is vertebral-radicular conflict. The absence of spinal symptoms and the beginning of pain in the buttocks and not in the lumbar region should reorient the etiologic search. Once a tumor of the nerve trunk has been ruled out (rarely responsible for pain other than that caused by tumor pressure), a myofascial syndrome should be explored searching for clinical, electrophysiological, and radiological evidence of compression of the sciatic trunk by the piriform muscle but also the obturator ...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2789333</comments>
            <pubDate>Mon, 07 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2789333</guid>        </item>
        <item>
            <title>[Endoscopy versus microsurgery: Results in a consecutive series of nonfunctioning pituitary adenomas.]</title>
            <link>http://www.medworm.com/index.php?rid=2775387&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19733369%26dopt%3DAbstract</link>
            <description>Authors: Kassis S, De Battista JC, G GR, Jacob M, Simon E, Rabilloud M, Froehlich P, Trouillas J, Borson-Chazot F, Perrin G, Jouanneau E
    Microsurgical removal of nonfunctioning pituitary adenomas (NFPAs) is often subtotal. Removing the blind spots as viewed through the microscope, endoscopic surgery may improve the quality of removal. Our purpose was to compare the results of the two techniques in a series of NFPA patients operated on by a single surgeon. Thirty-six patients with newly diagnosed NFPAs were operated on using a purely endoscopic procedure and 29 with a microsurgical technique. All patients were explored pre- and postoperatively (at 3 and 6 months and then every 12 months) by endocrine assays, ophthalmologic exam, and 3D MRI. The endocrine and ophthalmologic results as we...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2775387</comments>
            <pubDate>Wed, 02 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2775387</guid>        </item>
        <item>
            <title>[Odontoid process fracture in elderly patients over 70 years: Morbidity, handicap, and role of surgical treatment in a retrospective series of 27 cases.]</title>
            <link>http://www.medworm.com/index.php?rid=2661026&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19643449%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Odontoid fractures in the elderly are a very frequent problem. Immediate mortality is still high but appears correlated to associated lesions. Today's treatments must preserve autonomy for these patients. For elderly patients, the treatment must be chosen in relation to the fracture analysis. In our opinion, surgical management is the treatment of choice for unstable fractures (type II). Conservative management is indicated for stable fractures.
    PMID: 19643449 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2661026</comments>
            <pubDate>Mon, 27 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2661026</guid>        </item>
        <item>
            <title>[Isolated hypophyseal tuberculoma: Often mistaken.]</title>
            <link>http://www.medworm.com/index.php?rid=2622192&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19615704%26dopt%3DAbstract</link>
            <description>Authors: Salem R, Khochtali I, Jellali MA, Zrig A, Maatouk M, Jazerli N, Kriaa S, Affi T, Hafsa C, Kacem M, Golli M
    Hypophyseal tuberculoma is extremely rare and difficult to diagnose without a clearly suggestive context. Its radiologic features are not specific and are better recognized on MRI with a mass of a variable signal related to the percentage of caseous necrosis. A frequently associated thickening of the pituitary stalk suggests tuberculosis, requiring the search for another tuberculosis location. This paper reports an original case of hypophyseal tuberculoma since it occurred with no other tubercular infection, which delayed the diagnosis despite thickening of the pituitary stalk on MRI.
    PMID: 19615704 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2622192</comments>
            <pubDate>Tue, 14 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2622192</guid>        </item>
        <item>
            <title>[Severe orthostatic hypotension and intramedullary tumor: A case report and review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=2603119&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19592056%26dopt%3DAbstract</link>
            <description>We report an interesting case of severe OH that had complicated the surgical treatment of a high cervical spinal cord ependymoma and we review the literature.
    PMID: 19592056 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2603119</comments>
            <pubDate>Tue, 07 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2603119</guid>        </item>
        <item>
            <title>[Polyostotic fibrous dysplasia of the thoracic spine. A case study and review of the literature.]</title>
            <link>http://www.medworm.com/index.php?rid=2580861&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19577779%26dopt%3DAbstract</link>
            <description>We report the case of a 46-year-old woman admitted to the emergency department for subacute paraplegia. The spinal X-ray showed a spontaneous fracture at the T4-T5 level. The CT scan revealed a tumor infiltration of the vertebral body responsible for lysis. Spinal MRI confirmed the neoplasia also located in the epidural space with spinal cord compression. The patient underwent an emergency laminectomy associated with transpedicular screw fixation between the T2 and T6 levels. At 2 months, she had evolved to a normal gait. In the second session, a transthoracic approach was used for a bone-graft-assisted fusion procedure to achieve long-term stabilization. At 4 years, the bone fusion was excellent and the patient was able to resume socioprofessional activities. The diagnosis of fibrous dysp...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2580861</comments>
            <pubDate>Thu, 02 Jul 2009 23:00:00 +0100</pubDate>
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            <title>Tension pneumocephalus and rhinorrhea revealing spontaneous cerebrospinal fluid fistula of the anterior cranial base.</title>
            <link>http://www.medworm.com/index.php?rid=2524050&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19359019%26dopt%3DAbstract</link>
            <description>We report a case of spontaneous CSFF of the ethmoid cribriform plate presenting with rhinorrhea and tension pneumocephalus. We discuss the physiopathology, the radiological management, and the treatment of spontaneous CSF fistulas related to the anterior skull base. A 58-year-old woman was admitted to our institution for headaches with clear rhinorrhea persisting over several days. Antecedents were unremarkable. An episode of epistaxis three days before was reported. Clinical examination showed clear rhinorrhea, headaches, and anosmia. The CT scan showed voluminous epidural and subdural pneumocephalus with mass effect on both frontal and temporal lobes. A high-resolution CT scan with bone reconstruction showed a 2-mm bony defect of the cribriform plate. Surgery consisted of epidural fronta...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2524050</comments>
            <pubDate>Sun, 31 May 2009 23:00:00 +0100</pubDate>
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        <item>
            <title>[Early epidural hematoma after CSF shunt for obstructive hydrocephalus]</title>
            <link>http://www.medworm.com/index.php?rid=2524048&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19427004%26dopt%3DAbstract</link>
            <description>We present the first case of early epidural hematoma after CSF shunt probably caused by defective material. A 26-year-old man was treated for obstructive hydrocephalus associated with a tonsillar herniation, revealed by headaches and papillary edema. Ventriculoperitoneal shunt was preferred to endoscopic ventriculostomy. Three hours after the operation, the patient fell into a coma, developing a voluminous bifrontal epidural hematoma that was evacuated immediately. The patient completely recovered neurologically. One month later, to treat persistent hydrocephalus, endoscopic ventriculostomy was performed without incident. Then the shunt was removed and an opening threshold close to zero was discovered. Distant MRI showed a reduction in ventricular size, normalization of the tonsils' positi...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2524048</comments>
            <pubDate>Sun, 31 May 2009 23:00:00 +0100</pubDate>
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        <item>
            <title>[Follicular dural lymphoma. Case report]</title>
            <link>http://www.medworm.com/index.php?rid=2524047&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19428037%26dopt%3DAbstract</link>
            <description>Authors: Peltier J, Fichten A, Lefranc M, Toussaint P, Desenclos C, Pruvot AS, Nicot B, Le Gars D
    A case of a meningeal B-cell lymphoma is described. A 48-year-old man presented with an episode of grand mal seizure following a brain injury. An initial diagnosis of extradural hematoma was made based on the results of the cerebral computerized tomography scan. Magnetic resonance images demonstrated an enhanced mass with a dural tail attached to the meningeal layer of the temporal bone, suggesting a meningioma &quot;en plaque&quot;. The mass was surgically excised. Tumoral removal was subcomplete (Simpson 2). Operative inspection also suggested a meningioma, but histological analysis and electron microscopy revealed a grade IV follicular B-cell lymphoma. Biological studies were normal. An extensive...</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2524047</comments>
            <pubDate>Sun, 31 May 2009 23:00:00 +0100</pubDate>
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        <item>
            <title>[Multilevel contiguous injuries of the lower cervical spine during flexion trauma with delayed diagnosis: A case report.]</title>
            <link>http://www.medworm.com/index.php?rid=2524044&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19481230%26dopt%3DAbstract</link>
            <description>Authors: Uzel AP, Do L
    The authors report a case of bilateral C4-C5 facet fracture dislocation associated with a severe sprain underlying C5-C6, which had occurred during an traffic accident. The diagnosis of severe sprain was raised on the 55thday. The injury mechanism is studied. Contiguous multilevel injuries of the lower cervical spine should be suspected in case of high-energy trauma. MRI can provide an exhaustif diagnosis of possible multilevel injuries. After fixation of the obvious lesion, intraoperative dynamic fluoroscopy must be performed to demonstrate any instability in another area.
    PMID: 19481230 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2524044</comments>
            <pubDate>Tue, 26 May 2009 23:00:00 +0100</pubDate>
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            <title>[Surgical management of solitary eosinophilic granuloma of the calvaria. Two case reports.]</title>
            <link>http://www.medworm.com/index.php?rid=2524045&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19467681%26dopt%3DAbstract</link>
            <description>We present two cases of calvarial eosinophilic granulomas that were surgically removed. These tumors are reputed to have an excellent prognosis, even if local recurrences and systemic dissemination can occur during the follow-up. The authors discuss the pathogenesis and the evolutive profile but also the therapeutic management of solitary eosinophilic granuloma of the calvaria.
    PMID: 19467681 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2524045</comments>
            <pubDate>Mon, 18 May 2009 23:00:00 +0100</pubDate>
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        <item>
            <title>[Central neurocytoma: Case report.]</title>
            <link>http://www.medworm.com/index.php?rid=2524046&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19447451%26dopt%3DAbstract</link>
            <description>In this study, we report one case of central neurocytoma treated in our department. It is a benign tumor of the lateral ventricles of the brain with neuronal differentiation. The clinical symptoms mainly consisted in intracranial hypertension syndrome. Immunohistochemical studies are necessary for the histopathological diagnosis. The treatment of choice is surgical. To guarantee good progression, complete ablation is necessary. The clinical progression, radiological aspects, treatment, histopathology, and postoperative progression will be discussed.
    PMID: 19447451 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2524046</comments>
            <pubDate>Thu, 14 May 2009 23:00:00 +0100</pubDate>
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            <title>[Intraorbital dermoid cyst: Case report.]</title>
            <link>http://www.medworm.com/index.php?rid=2524049&amp;cid=s_36795_153_f&amp;fid=36795&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19368946%26dopt%3DAbstract</link>
            <description>Authors: Taha S, Doe K, Compeyre S, Nogues L, Lopes M, Leriche B
    Dermoid cysts account for 3-4% of primary orbital tumors. The intraorbital location is relatively rare. The authors report a case of a 12-year-old male with an intraorbital dermoid cyst revealed by progressive right proptosis. The imaging aspects (CT scan and MRI) were consistent with intraconic dermoid cyst. The tumor was extirpated via a subfrontal approach. Histopathologic examination confirmed the diagnosis of dermoid cyst. The authors discuss the clinical symptoms, radiological aspects, and management.
    PMID: 19368946 [PubMed - as supplied by publisher] (Source: Neuro-Chirurgie)</description>
            <author>Neuro-Chirurgie</author>
            <type>journals</type>
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            <pubDate>Sun, 12 Apr 2009 23:00:00 +0100</pubDate>
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