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        <title>Head and Neck Pathology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Head and Neck Pathology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Head+and+Neck+Pathology&t=Head+and+Neck+Pathology&s=Search&f=source]]></link>
        <lastBuildDate>Thu, 09 Feb 2012 00:42:12 +0100</lastBuildDate>
        <item>
            <title>Disseminated Carcinoma Ex Pleomorphic Adenoma in an Adolescent Confirmed by Application of PLAG1 Immunohistochemistry and FISH for PLAG1 Rearrangement</title>
            <link>http://www.medworm.com/index.php?rid=5661206&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb7812531203v3471%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 16-year-old previously asymptomatic boy presented with complaints of fatigue, weight loss, and back pain for several months.
 Imaging studies revealed a large superior mediastinal mass, numerous bilateral pulmonary nodules, and multiple lytic bone
 lesions. A needle biopsy from a sternal lesion showed a poorly differentiated carcinoma, immunoreactive for cytokeratins and
 EMA and immunonegative for various organ/tissue-specific markers. His past medical history was significant for excision of
 a parotid gland tumor 5&amp;nbsp;years earlier. Histologic review of the salivary gland tumor revealed a pleomorphic adenoma containing
 a microscopic focus of invasive carcinoma (carcinoma ex pleomorphic adenoma). By immunohistochemistry, both the salivary gland
 tumor and the diss...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5661206</comments>
            <pubDate>Wed, 01 Feb 2012 17:13:46 +0100</pubDate>
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        <item>
            <title>Frontal Sinus Osteoma with Osteoblastoma-like Histology and Associated Intracranial Pneumatocele</title>
            <link>http://www.medworm.com/index.php?rid=5639888&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fal660w71275u6368%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteomas of the cranial sinuses are rare, benign bony tumors that can be complicated by the formation of an intracranial pneumatocele.
 If not treated promptly, a pneumatocele can lead to abscess formation, meningitis, or ventriculitis. In the present case,
 an intracerebral pneumatocele was formed when an 18&amp;nbsp;cm3 osteoma breached the posterior wall of the frontal sinus creating a one-way valve through which air could enter the intracranial
 cavity. The patient presented after forceful sneezing with nonspecific symptoms of headache, nausea, and vomiting. CT demonstrated
 a frontal collection of loculated air with mass effect within the left cerebral hemisphere. A partly mineralized mass occupied
 the left superior nasal ethmoid sinus and left frontal sinus. Of inter...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639888</comments>
            <pubDate>Tue, 24 Jan 2012 18:14:59 +0100</pubDate>
            <guid isPermaLink="false">5639888</guid>        </item>
        <item>
            <title>Intercalated Duct Lesion of the Parotid</title>
            <link>http://www.medworm.com/index.php?rid=5639889&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj773w24288687141%2F</link>
            <description>We present the case of a 63-year-old woman diagnosed with an intercalated duct lesion of the parotid.
 Her case is illustrative of the difficulty and importance of an accurate pathologic diagnosis in the management of patients
 with these lesions.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-4DOI 10.1007/s12105-012-0329-8Authors
		Matthew R. Naunheim, Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, MA, USAHarrison W. Lin, Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, MA, USAWilliam C. Faquin, Department of Pathology, Massachusetts General Hospital, Boston, MA, USADerrick T. Lin, Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639889</comments>
            <pubDate>Tue, 24 Jan 2012 07:15:35 +0100</pubDate>
            <guid isPermaLink="false">5639889</guid>        </item>
        <item>
            <title>Well-Differentiated Liposarcoma/Atypical Lipomatous Tumor of the Oral Cavity: Report of Three Cases and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=5585687&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh183223223rh1725%2F</link>
            <description>In this study, three additional cases of ALT/WDLS located on the tongue (2 cases) and
 the lower lip (1 case), respectively, are described. Analysis of the salient clinicopathologic features of 63 oral ALT/WDLS
 cases previously reported in the English language literature, as well as of the 3 cases presented in this study, indicates
 that the indolent biologic behavior of this tumor justifies its designation as a locally spreading malignant neoplasm, affording
 a rather conservative surgical approach.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-10DOI 10.1007/s12105-011-0327-2Authors
		Evangelia Piperi, Department of Oral Pathology and Medicine, Dental School, University of Athens, 2 Thivon Street, 11527 Athens, GreeceKonstantinos I. Tosios, Department of Oral Pathology and...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5585687</comments>
            <pubDate>Tue, 10 Jan 2012 17:02:08 +0100</pubDate>
            <guid isPermaLink="false">5585687</guid>        </item>
        <item>
            <title>Cytoplasmic Ezrin and Moesin Correlate with Poor Survival in Head and Neck Squamous Cell Carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5573444&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa85k0t387m444844%2F</link>
            <description>This study supports our previous findings associating cytoplasmic
 ezrin with more aggressive behavior and poorer outcome and indicates the need for a multi-institutional study to validate
 the use of cytoplasmic ezrin as a biomarker for treatment planning in head and neck squamous cell carcinoma.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-12DOI 10.1007/s12105-011-0328-1Authors
		Nicolas F. Schlecht, Department of Epidemiology and Population Health, Albert Einstein College of Medicine and Montefiore Medical Center, 1300 Morris Park Avenue, Bronx, NY 10461, USAMargaret Brandwein-Gensler, Department of Pathology, University of Alabama Birmingham, Birmingham, AL 35249, USARichard V. Smith, Department of Otorhinolaryngology, Head and Neck Surgery, Albert Einstein College o...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573444</comments>
            <pubDate>Fri, 06 Jan 2012 16:47:34 +0100</pubDate>
            <guid isPermaLink="false">5573444</guid>        </item>
        <item>
            <title>Epithelial Salivary Gland Tumors in Two Distant Geographical Locations, Finland (Helsinki and Oulu) and Israel (Tel Aviv): A 10-Year Retrospective Comparative Study of 2,218 Cases</title>
            <link>http://www.medworm.com/index.php?rid=5573445&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F12p326x7356k4783%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Salivary gland tumors (SGTs) of epithelial origin are relatively rare, and worldwide reports show considerable variations
 in their epidemiology. The aim of this study was to examine, for the first time, the records of SGTs from two very distant
 geographical locations, Finland (two medical centers) and Israel (one medical center) between 1999 and 2008, based exclusively
 on the 2005 WHO classification of head and neck tumors, and to compare those data to the other available (single-center) studies
 that used the same classification. A total of 2,218 benign and malignant tumors diagnosed in the three centers were analyzed.
 Differences in classification of the tumors were found between the two geographical locations as well as between the two centers
 from Finland. Ther...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573445</comments>
            <pubDate>Fri, 06 Jan 2012 16:47:33 +0100</pubDate>
            <guid isPermaLink="false">5573445</guid>        </item>
        <item>
            <title>Mucosal Pigmentation Caused by Imatinib: Report of Three Cases</title>
            <link>http://www.medworm.com/index.php?rid=5562679&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F217g575885161w23%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Imatinib mesylate (STI-571, Gleevec®), a tyrosine kinase inhibitor, is a first-line medication for treating chronic myeloid leukemia (CML). Clinical studies revealed
 very good hematological responses without significant side effects. However, imatinib may lead to mucosal pigmentation. Three
 patients, two males aged 64 and 53 and one female aged 29 presented with a painless, diffuse, grey-blue pigmentation of the
 mucosa of the hard palate. Both male patients had a history of CML and had been on imatinib for 4 and 10&amp;nbsp;years, respectively.
 The female patient had been on imatinib for 4&amp;nbsp;years for pelvic fibromatosis. Histopathologically, deposition of fine, dark-brown,
 spherical granules was noted within the connective tissue. There was no inflammation or hemo...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562679</comments>
            <pubDate>Fri, 30 Dec 2011 16:49:59 +0100</pubDate>
            <guid isPermaLink="false">5562679</guid>        </item>
        <item>
            <title>Metastatic Papillary Thyroid Carcinoma to the Maxilla: Case Report and Literature Review</title>
            <link>http://www.medworm.com/index.php?rid=5562680&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl4r68k66g29p63r2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Metastatic tumors to the oral cavity are uncommon and a thyroid origin is considered exceedingly rare. A case of metastatic
 papillary thyroid carcinoma (PTC) presenting as a painful swelling in the right posterior maxilla of a 63-year-old male is
 reported here. The patient had been diagnosed with PTC 2&amp;nbsp;years ago and treated with thyroidectomy and radioactive iodine treatment.
 Radiographically, the metastatic lesion presented as a poorly-defined radiolucent lesion around an impacted maxillary third
 molar in the right maxilla. Histopathologic examination revealed features of PTC which was immunohistochemically positive
 for pancytokeratin, keratin 19 and thyroglobulin. Imaging studies revealed the presence of residual maxillary and neck disease
 as well as additi...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562680</comments>
            <pubDate>Fri, 30 Dec 2011 07:09:11 +0100</pubDate>
            <guid isPermaLink="false">5562680</guid>        </item>
        <item>
            <title>Small Biopsy Specimens Reliably Indicate p16 Expression Status of Oropharyngeal Squamous Cell Carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5553748&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa3wn63381876155j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Human papillomavirus (HPV)—related oropharyngeal squamous cell carcinoma (SCC) is associated with favorable patient survival.
 Tumor HPV status at primary diagnosis is critical for proper management, and p16 immunohistochemistry (IHC) has emerged as
 a reliable, single, surrogate marker. It is not known, however, if small biopsy specimens are completely adequate for p16
 evaluation. From a database of oropharyngeal SCC for which p16 IHC and histologic typing were already performed, all patients
 (32) who had available in-house primary tumor biopsy specimens and also subsequent surgical resections were analyzed. p16
 IHC was performed along with histologic typing into: Type 1 keratinizing SCC, Type 2 nonkeratinizing SCC with maturation,
 and Type 3 nonkeratinizing SCC....</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5553748</comments>
            <pubDate>Tue, 27 Dec 2011 16:49:47 +0100</pubDate>
            <guid isPermaLink="false">5553748</guid>        </item>
        <item>
            <title>Solitary Langerhans Histiocytosis of the Thyroid Gland: A Case Report and Literature Review</title>
            <link>http://www.medworm.com/index.php?rid=5546086&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm234746856344735%2F</link>
            <description>We present an unusual case of LCH of the thyroid gland, with variable
 diagnoses on fine needle aspiration (FNA) cytology, and literature review of all English reported cases.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-11DOI 10.1007/s12105-011-0321-8Authors
		Darren K. Patten, Department of Biosurgery and Surgical Oncology, St Mary’s Hospital, Imperial College Healthcare NHS Trust, London, W2 1NY UKZubair Wani, Department of Accident and Emergency Medicine, The Horton General Hospital, Oxford, UKNeil Tolley, Department of Endocrine Surgery, Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5546086</comments>
            <pubDate>Fri, 23 Dec 2011 16:53:41 +0100</pubDate>
            <guid isPermaLink="false">5546086</guid>        </item>
        <item>
            <title>Imaging and Histopathological Features of Jacob’s Disease: A Case Study</title>
            <link>http://www.medworm.com/index.php?rid=5546087&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw657585841786617%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A pathologically elongated coronoid process forming a joint with the zygomatic arch and bone is termed as “Jacob’s disease.”
 Herein, we present a case of Jacob’s disease, which has rarely been reported in the literature. Moreover, very few cases have
 been reported from the Indian subcontinent. A 28&amp;nbsp;years-old male reported to us with progressive restriction of mouth opening.
 After detailed imaging, coronoidectomy was performed through an intraoral approach. A mushroom-shaped gross specimen was obtained.
 Osteochondroma of the coronoid process was diagnosed based on the histopathologic examination of the excised tissue. Although
 Jacob’s disease is seldom considered in the list of differential diagnoses for restricted mouth opening, our case highlights
 ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5546087</comments>
            <pubDate>Wed, 21 Dec 2011 20:07:58 +0100</pubDate>
            <guid isPermaLink="false">5546087</guid>        </item>
        <item>
            <title>Sinonasal Tract Mucoepidermoid Carcinoma: A Clinicopathologic and Immunophenotypic Study of 19 Cases Combined with a Comprehensive Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=5527643&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F24j187800w743822%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Primary sinonasal tract mucoepidermoid carcinomas (MEC) are uncommon tumors that are frequently misclassified, resulting in
 inappropriate clinical management. The design of this study is retrospective. Nineteen cases of MEC included 10 females and
 9 males, aged 15–75&amp;nbsp;years (mean, 52.7&amp;nbsp;years); males, on average were younger by a decade than females (47.2 vs. 57.7 years).
 Patients presented most frequently with a mass, obstructive symptoms, pain, and/or epistaxis present for a mean of 12.6&amp;nbsp;months.
 The majority of tumors involved the nasal cavity alone (n&amp;nbsp;=&amp;nbsp;10), maxillary sinus alone (n&amp;nbsp;=&amp;nbsp;6), or a combination of the nasal
 cavity and paranasal sinuses (n&amp;nbsp;=&amp;nbsp;3) with a mean size of 2.4&amp;nbsp;cm. Most patients presented at a lo...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5527643</comments>
            <pubDate>Mon, 19 Dec 2011 16:50:02 +0100</pubDate>
            <guid isPermaLink="false">5527643</guid>        </item>
        <item>
            <title>External Auditory Osteoma</title>
            <link>http://www.medworm.com/index.php?rid=5527644&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh8v686003401w172%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;External auditory canal (EAC) osteomas are rare, benign bony neoplasms that occur in wide range of patients. While chronic
 irritation and inflammation have been suggested as causal factors in several cases, significant data is lacking to support
 these suspicions. Symptoms are rare and can include hearing loss, vertigo, pain and tinnitus. Diagnosis is made based on a
 combination of clinical history and examination, radiographic imaging, and histopathology. Osteomas of the EAC are usually
 found incidentally and are unilateral and solitary. Computed tomography reveals a hyperdense, pedunculated mass arising from
 the tympanosquamous suture and lateral of the isthmus. Histopathologically, EAC osteomas are covered with periosteum and squamous
 epithelium, and consist of ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5527644</comments>
            <pubDate>Mon, 19 Dec 2011 16:50:00 +0100</pubDate>
            <guid isPermaLink="false">5527644</guid>        </item>
        <item>
            <title>Sclerosing Polycystic Adenosis</title>
            <link>http://www.medworm.com/index.php?rid=5527645&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F82nt8158h5678211%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 25-year-old female presented with a well-defined, painless mass of 1&amp;nbsp;year’s duration in the right parotid gland. MR imaging
 revealed a relatively well-circumscribed lesion involving the deep and superficial lobes of the right parotid gland. Histologic
 examination of the resection resulted in a diagnosis of sclerosing polycystic adenosis, a rare benign salivary gland entity
 of presumed non-neoplastic origin. The clinical, radiographic, and morphologic features of sclerosing polycystic adenosis
 are discussed.
 
 
	Content Type Journal ArticleCategory Sine qua non Radiology-PathologyPages 1-3DOI 10.1007/s12105-011-0317-4Authors
		Colin A. Eliot, Naval Postgraduate Dental School, Bethesda, MD, USAAlice B. Smith, Uniformed Service University of the Health Scienc...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5527645</comments>
            <pubDate>Mon, 19 Dec 2011 16:49:58 +0100</pubDate>
            <guid isPermaLink="false">5527645</guid>        </item>
        <item>
            <title>Prognostic Significance of Regulators of Cell Cycle and Apoptosis, p16INK4a, p53, and bcl-2 in Primary Mucosal Melanomas of the Head and Neck</title>
            <link>http://www.medworm.com/index.php?rid=5507283&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F025421165061hn55%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Abnormalities in cell cycle regulation, tumor suppressor gene functions and apoptosis are frequent events in tumorigenesis.
 Their role in the pathogenesis and prognosis of primary mucosal melanomas (MM) of the upper aerodigestive tract remains unknown.
 Sixty-four patients (40 men, 24 women, median age 64&amp;nbsp;years) with MM were included in this study; 32 had tumors in the nasal/paranasal
 cavities, 28 in the oral cavity and 4 in the pharynx. Archival tissues from 47 initial mucosal tumors, 17 mucosal recurrences,
 and 13 nodal/distant metastases were subjected to immunohistochemistry using antibodies against p16, p53, and bcl-2. The results
 were correlated with histological features and survival data. Expressions of p16, p53, and bcl-2 proteins were seen in 25%
 (N&amp;...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5507283</comments>
            <pubDate>Mon, 12 Dec 2011 17:16:55 +0100</pubDate>
            <guid isPermaLink="false">5507283</guid>        </item>
        <item>
            <title>The Dynamics of Oral Lichen Planus: A Retrospective Clinicopathological Study</title>
            <link>http://www.medworm.com/index.php?rid=5507284&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7p474r63658870u4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To evaluate disease dynamics, treatment results, and frequency of malignant transformation. Ten-year single center retrospective
 study. The study included 171 patients, 28–99&amp;nbsp;years old. Follow-up was 1–16&amp;nbsp;years. 49.5% exhibited changes in clinical presentation,
 with 19% yearly increase of probability for type shift. Index of extent (number of oral locations) showed a mean 40% decrease
 and 94.1% reported improvement. There were significant differences between treated and untreated patients (P&amp;nbsp;=&amp;nbsp;0.012). Patients with or without systemic diseases had identical treatment requirements for oral lesions. The prevalence
 of SCC was 5.8%. Oral lichen planus constantly changes presentation and extent of involvement. The effect of systemic diseases
 was ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5507284</comments>
            <pubDate>Mon, 12 Dec 2011 17:16:54 +0100</pubDate>
            <guid isPermaLink="false">5507284</guid>        </item>
        <item>
            <title>Segmental Odontomaxillary Dysplasia: Report of 3 Cases and Literature Review</title>
            <link>http://www.medworm.com/index.php?rid=5478723&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg556107m73963314%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Segmental Odontomaxillary Dysplasia (SOD) is an uncommon developmental disorder of unknown etiology that causes a unilateral
 alteration of the maxilla associated with an abnormal growth and maturation of bone, lack of one or both premolars and delayed
 tooth eruption on the affected side, alteration of adjacent gingival tissue with or without facial cutaneous lesions. Radiographically
 is observed an irregular trabecular pattern and reduction of the maxillary sinus. There are 50 cases reported in the English-language
 literature. A literature review is herein presented emphasizing the clinical, radiographic, and histological features, and
 three additional cases of SOD affecting a 22&amp;nbsp;years-old woman, a 18&amp;nbsp;years-old man, and a 5&amp;nbsp;years-old boy, respectivel...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5478723</comments>
            <pubDate>Fri, 02 Dec 2011 17:28:07 +0100</pubDate>
            <guid isPermaLink="false">5478723</guid>        </item>
        <item>
            <title>Sinonasal Myospherulosis and Paraffin Retention Cysts Suggested by CT: Report of a Case</title>
            <link>http://www.medworm.com/index.php?rid=5470569&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd0t118332272912q%2F</link>
            <description>We report a case found in a 79-year-old female 8&amp;nbsp;months after functional
 endoscopic sinus surgery during which sinus cavities had been packed with gauze coated with Terra-Cortril (a paraffin-based
 tetracycline/steroid ointment). The preoperative diagnosis was suggested during CT of the paranasal sinuses by the presence
 of macroscopic paraffin retention cysts having a characteristic fat density. To our knowledge, our case represents the first
 report of sinonasal myospherulosis suggested by CT.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-5DOI 10.1007/s12105-011-0310-yAuthors
		Bruno Coulier, Department of Medical Imaging, Clinique St Luc, 5004 Bouge, Namur, BelgiumOlivier Desgain, Department of Otorhinolaryngology, Clinique St Luc, 5004 Bouge, Namur, BelgiumIsabelle...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5470569</comments>
            <pubDate>Wed, 30 Nov 2011 04:38:26 +0100</pubDate>
            <guid isPermaLink="false">5470569</guid>        </item>
        <item>
            <title>Re-Evaluating Historic Cohort of Salivary Acinic Cell Carcinoma with New Diagnostic Tools</title>
            <link>http://www.medworm.com/index.php?rid=5470568&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw1771753885w6472%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mammary analogue secretory carcinoma (MASC) was recently identified as a distinct salivary gland neoplasm, morphologically
 resembling intercalated duct cell predominant acinic cell carcinoma (AciCC). To determine how frequently MASC has mimicked
 an intercalated duct cell predominant AciCC, we reviewed AciCC diagnosed from 1956 to 1975. Nine AciCC consecutively diagnosed
 in that period were identified. Based on morphologic examination, one case diagnosed as AciCC in a male patient in 1960 was
 re-classified as MASC [confirmed by fluorescence in situ hybridization (FISH) showing ETV6 translocation]. Another case diagnosed as AciCC of the palate in a female patient in 1975 was re-classified as mucoepidermoid
 carcinoma (based on the lack of acinar differentiation, prese...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5470568</comments>
            <pubDate>Wed, 30 Nov 2011 04:38:26 +0100</pubDate>
            <guid isPermaLink="false">5470568</guid>        </item>
        <item>
            <title>Lip Ulceration Associated with Intravenous Administration of Zoledronic Acid: Report of a Case</title>
            <link>http://www.medworm.com/index.php?rid=5443562&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F02r763p7lr873j33%2F</link>
            <description>This report,
 for the first time, describes the mucosal ulceration related to intravenous use of zoledronic acid (ZA). A 52-year-old female
 patient presented with painful ulcers on both cutaneous/mucosal surfaces of the lower lip and a 2-month history of osteonecrosis
 of the mandible beside the right lower canine. Her medical record included intravenous administration of ZA for 10&amp;nbsp;months
 for primary breast cancer metastatic to bone. Examination of the peripheral blood showed severe anemia and a slightly increased
 white blood cell count, due to urinary tract infection by E. coli, but no evidence of a viral infection. The treatment of anemia and E. coli infection did not improve the labial ulcers. Biopsy from the mucosal lesion revealed a non-specific ulceration with moderate
 infla...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5443562</comments>
            <pubDate>Mon, 21 Nov 2011 18:08:27 +0100</pubDate>
            <guid isPermaLink="false">5443562</guid>        </item>
        <item>
            <title>P27/SKP-2 Histochemical Profile is Relevant to Malignant Salivary Gland Tumors (MST) Histogenesis and Tumor Grade</title>
            <link>http://www.medworm.com/index.php?rid=5433477&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcun1p4j2421g1548%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Malignant salivary gland tumors (MST) represent over more than 24 distinct morphological subtypes. Most high grade tumors
 arise from the excretory duct portion of the salivary gland apparatus; the remainder from the intercalated duct portion. Altered
 p27/skp-2 expression has been associated with tumor aggressiveness and histologic differentiation. In our study, we analyzed
 p27/skp-2 expression proteins on series of malignant salivary gland tumors in order to assess their value as a histogenetic
 marker, which is relevant to tumor grade. 61 MST cases were segregated by proposed histogenesis and immunohistochemistry was
 performed using antibodies directed against p27 and skp-2. MST of proposed intercalated duct origin (n&amp;nbsp;=&amp;nbsp;27) showed strong p27 expression (n...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5433477</comments>
            <pubDate>Fri, 18 Nov 2011 06:55:18 +0100</pubDate>
            <guid isPermaLink="false">5433477</guid>        </item>
        <item>
            <title>Bizarre Parosteal Osteochondromatous Proliferation (Nora’s Lesion) of the Mandible. A Rare Bony Lesion</title>
            <link>http://www.medworm.com/index.php?rid=5433478&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu4qqg23t301n0411%2F</link>
            <description>We present
 a rare case of BPOP involving the mandible in a 10&amp;nbsp;year old African American male. Microscopically, a fibro-cartilaginous
 cap giving rise to a proliferation of variably mineralized osteophytic finger-like projections of bone was seen. Multiple
 trabeculae of “blue bone” were noted as well as numerous atypical appearing chondrocytes. The lesion recurred within 4&amp;nbsp;months
 following the initial excision but has not recurred to date after the second local excision. To the best of our knowledge,
 this is the first report of BPOP arising in the mandible. In addition, we discuss the clinical and microscopic features, differential
 diagnosis, and prognosis of this rare entity. We present a case of BPOP of the mandible and believe this is the first report
 of such a case i...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5433478</comments>
            <pubDate>Fri, 18 Nov 2011 06:55:17 +0100</pubDate>
            <guid isPermaLink="false">5433478</guid>        </item>
        <item>
            <title>Lack of Association of Cadherin Expression and Histopathologic Type, Metastasis, or Patient Outcome in Oropharyngeal Squamous Cell Carcinoma: A Tissue Microarray Study</title>
            <link>http://www.medworm.com/index.php?rid=5411593&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh73h462w761uk566%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Altered cadherin expression is important for metastasis in many carcinomas including head and neck squamous cell carcinoma
 (SCC). We evaluated E- and N-cadherin expression specifically in oropharyngeal SCC and correlated this with clinical and pathologic
 features. Oropharyngeal SCC patients with clinical follow up information were identified from clinician databases from 1996
 through 2007 and tissue microarrays created. Tumors had been previously typed histopathologically as keratinizing, non-keratinizing,
 or non-keratinizing with maturation, and had known p16 and human papillomavirus status, respectively. Immunohistochemistry
 was performed on the microarrays, and staining was evaluated for presence and intensity (0&amp;nbsp;=&amp;nbsp;negative, 1&amp;nbsp;=&amp;nbsp;weak, 2&amp;nbsp;...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5411593</comments>
            <pubDate>Wed, 09 Nov 2011 17:58:34 +0100</pubDate>
            <guid isPermaLink="false">5411593</guid>        </item>
        <item>
            <title>Metastasis of Occult Prostatic Carcinoma to the Sphenoid Sinus: Report of a Rare Case and a Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=5391007&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl1351520m6k70v57%2F</link>
            <description>We present a case (55-year-old) with a metastasis to the sphenoid sinus from an occult prostatic adenocarcinoma as the first
 evidence of disease. The patient’s symptoms were progressive left-sided headache of a few months duration and a 2-week history
 of blurred vision with diplopia. Clinical examination revealed a left cranial nerve III palsy and ptosis. A computed tomography
 scan showed a 2&amp;nbsp;cm large, well delineated soft tissue lesion involving the left sphenoid sinus and extending to the left cavernous
 sinus with sclerosis of the adjacent sphenoid bone. Histological and immunohistochemical examinations revealed a poorly differentiated
 adenocarcinoma that was positive for prostate specific antigen (PSA) and broad-spectrum cytokeratins (Cam 5.2). Subsequent
 urological examina...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5391007</comments>
            <pubDate>Fri, 04 Nov 2011 05:44:45 +0100</pubDate>
            <guid isPermaLink="false">5391007</guid>        </item>
        <item>
            <title>In Situ Hybridization Signal Patterns in Recurrent Laryngeal Squamous Papillomas Indicate that HPV Integration Occurs at an Early Stage</title>
            <link>http://www.medworm.com/index.php?rid=5391006&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F520560u777760318%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Laryngeal papillomas are benign tumors that frequently recur and can compromise airways. We investigated HPV genotype, physical
 status, and protein expression in juveniles versus adults. Thirty-five laryngeal papilloma specimens were obtained from ten
 juveniles (1–16&amp;nbsp;years) and eleven adults (24–67&amp;nbsp;years). In cases of recurrent papillomatosis (7 juveniles, 7 adults), the
 first and last papillomas were assayed. HPV type was determined by GP5+/6+ PCR and dot blot hybridization. In situ hybridization
 (ISH) was performed on 34 specimens; the data were recorded in terms of diffuse (episomal HPV) and punctate (integrated HPV)
 signal patterns. Immunohistochemistry for the HPV L1 capsid protein, a marker of HPV productive status, was performed on 32
 samples....</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5391006</comments>
            <pubDate>Fri, 04 Nov 2011 05:44:45 +0100</pubDate>
            <guid isPermaLink="false">5391006</guid>        </item>
        <item>
            <title>Parotid Gland Solitary Fibrous Tumor: A Case Report and Clinicopathologic Review of 22 Cases from the Literature</title>
            <link>http://www.medworm.com/index.php?rid=5325928&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff627074jw676l580%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Solitary fibrous tumors (SFTs) are rare tumors in the head and neck, and even more so in the parotid gland. The mass-like
 clinical presentation and histologic features result in frequent misclassification, resulting in inappropriate clinical management.
 There are only a few reported cases in the English literature. Twenty-one patients with parotid gland solitary fibrous tumor
 were compiled from the English literature (Medline 1960–2011) and integrated with this case report. The patients included
 11 males and 11 females, aged 11–79&amp;nbsp;years (mean, 51.2&amp;nbsp;years), who presented with a parotid gland painless mass gradually increasing
 in size or with compression symptoms, with a mean duration of symptoms of 24.7&amp;nbsp;months. The mean tumor size was 4.5&amp;nbsp;cm....</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325928</comments>
            <pubDate>Sat, 15 Oct 2011 15:47:59 +0100</pubDate>
            <guid isPermaLink="false">5325928</guid>        </item>
        <item>
            <title>Angiosarcoma Arising from the Tongue of an 11-Year-Old Girl with Xeroderma Pigmentosum</title>
            <link>http://www.medworm.com/index.php?rid=5317329&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F54257522tg77j871%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Xeroderma pigmentosum (XP) is a rare autosomal recessive defect in DNA endonuclease activity that is associated with the development
 of cutaneous malignancies, at sun exposed sites, including basal cell carcinoma, squamous cell carcinoma, and melanoma. Squamous
 cell carcinomas are also known to target the anterior tongue. Patients sometimes develop angiosarcomas, and these invariably
 arise from sun-exposed skin. A biopsy was taken from a large mass arising in the anterior tongue of an 11-year-old girl with
 XP and a history of cutaneous basal cell carcinomas. The histopathologic findings demonstrated a high grade epithelioid neoplasm
 resembling a poorly differentiated squamous cell carcinoma, but the immunohistochemical profile (AE1/AE3 negative, p63 negative,
 CD31...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5317329</comments>
            <pubDate>Mon, 10 Oct 2011 15:05:15 +0100</pubDate>
            <guid isPermaLink="false">5317329</guid>        </item>
        <item>
            <title>Lip Nodules Caused by Hyaluronic Acid Filler Injection: Report of Three Cases</title>
            <link>http://www.medworm.com/index.php?rid=5306564&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1620266x32h8l608%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
	Content Type Journal ArticleCategory Original PaperPages 1-5DOI 10.1007/s12105-011-0304-9Authors
		Shokoufeh Shahrabi Farahani, Harvard School of Dental Medicine, 49 Worthington Street #7, Boston, MA 02120, USAJohn Sexton, Wellesley, MA, USAJeffrey D. Stone, Lowell, MA, USAKevin Quinn, N. Dartmouth, MA, USASook-Bin Woo, Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Boston, MA, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5306564</comments>
            <pubDate>Fri, 07 Oct 2011 15:58:23 +0100</pubDate>
            <guid isPermaLink="false">5306564</guid>        </item>
        <item>
            <title>Expression of the Vascular Endothelial Growth Factor and Angiopoietins in Mucoepidermoid Carcinoma of Salivary Gland</title>
            <link>http://www.medworm.com/index.php?rid=5263425&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4p5542021j83341n%2F</link>
            <description>In this study, we have analyzed by immunohistochemistry the expression
 of VEGF, Ang-1, Ang-2 and the Angs receptor Tie2 in both the stroma and tumor cells of mucoepidermoid carcinoma (MEC) of salivary
 gland. We have demonstrated that when myofibroblasts were detected adjacent to the cancer cells, they were frequently associated
 with intense positive staining for Ang-1 and Ang-2, and no reactivity to VEGF and Tie2. These myofibroblast-rich Ang-1 and
 Ang-2-stained areas were more commonly found in high-grade MEC cases than in low-grade ones. As for the malignant cells, they
 frequently expressed all proteins studied, but Ang-2 and VEGF were detected at higher levels compared to Ang-1 and Tie2. Our
 results indicate that the MEC environment favors cooperative activity between Angs and VEG...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5263425</comments>
            <pubDate>Sat, 24 Sep 2011 15:47:01 +0100</pubDate>
            <guid isPermaLink="false">5263425</guid>        </item>
        <item>
            <title>Colonic-Type Adenocarcinoma of the Base of the Tongue: A Case Report of a Rare Neoplasm</title>
            <link>http://www.medworm.com/index.php?rid=5263426&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkm2380j3512x415x%2F</link>
            <description>We present an additional case of lingual
 intestinal-type adenocarcinoma with mucinous features that occurred in association with cervical node metastasis and discuss
 the clinicopathologic features and histogenetic aspects of this rare entity.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-5DOI 10.1007/s12105-011-0301-zAuthors
		Denisa Slova, Department of Pathology and Laboratory Medicine, St. Luke’s-Roosevelt Hospital Center, Columbia University College of Physicians and Surgeons, St. Luke’s Division, Clark 4, 1111 Tenth Avenue, New York, NY 10025, USAAlberto Paniz Mondolfi, Department of Pathology and Laboratory Medicine, St. Luke’s-Roosevelt Hospital Center, Columbia University College of Physicians and Surgeons, St. Luke’s Division, Clark 4, 1111 Tenth Avenue, N...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5263426</comments>
            <pubDate>Sat, 24 Sep 2011 15:47:00 +0100</pubDate>
            <guid isPermaLink="false">5263426</guid>        </item>
        <item>
            <title>Ganglioneuroblastic Transformation in Olfactory Neuroblastoma</title>
            <link>http://www.medworm.com/index.php?rid=5228698&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6685v5081nn252j1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ganglioneuroblastic transformation in olfactory neuroblastoma (ONB) is an exceptionally rare phenomenon. We document the case
 of a patient with a poorly differentiated sinonasal malignancy that recurred following treatment with chemoradiotherapy and
 showed ganglioneuroblastic transformation. Although the index tumour showed neuroendocrine differentiation, it did not have
 the typical clinico-pathological features associated with ONB. We highlight the diagnostic difficulties in establishing an
 accurate diagnosis for undifferentiated sinonasal tumours and present evidence that the index tumour was an ONB. The current
 report is only the third case of ONB showing complete ganglioneuroblastic transformation.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-6D...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5228698</comments>
            <pubDate>Wed, 14 Sep 2011 05:51:06 +0100</pubDate>
            <guid isPermaLink="false">5228698</guid>        </item>
        <item>
            <title>Glandular Odontogenic Cyst: Analysis of 46 Cases with Special Emphasis on Microscopic Criteria for Diagnosis</title>
            <link>http://www.medworm.com/index.php?rid=5228697&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx1w0107p453071u5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The glandular odontogenic cyst (GOC) is now a relatively well-known entity with recent reviews indicating over 100 cases reported
 in the English literature. The GOC’s importance relates to the fact that it exhibits a propensity for recurrence similar to
 the odontogenic keratocyst, and that it may be confused microscopically with central mucoepidermoid carcinoma (CMEC). Numerous
 histopathologic features for the GOC have been described, but the exact microscopic criteria necessary for diagnosis have
 not been universally accepted. Furthermore, some of the microscopic features of GOC may also be found in dentigerous, botryoid,
 radicular, and surgical ciliated cysts. The purpose of this multicenter retrospective study is to further define the clinical,
 radiographic, ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5228697</comments>
            <pubDate>Wed, 14 Sep 2011 05:51:06 +0100</pubDate>
            <guid isPermaLink="false">5228697</guid>        </item>
        <item>
            <title>The Challenges of Defining Oral Cancer: Analysis of an Ontological Approach</title>
            <link>http://www.medworm.com/index.php?rid=5228699&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F517jh80w64577858%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;An important inconsistency currently exists in the literature on oral cancer. Reviewing this literature, one finds that the
 term oral cancer is defined and described with great variation. In a search in PubMed, at least 17 different terms were found
 for titles of papers reporting data on oral cancer. The variability of the terms used for designating anatomic regions and
 type of malignant neoplasms for reporting oral cancer has hampered the ability of researchers to effectively retrieve information
 concerning oral cancer. Therefore, it is sometimes extremely difficult to provide meaningful comparisons among various studies
 of oral cancer. Recently, a new ontological strategy that is rooted in consensus-based controlled vocabularies has been proposed
 to improve the ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5228699</comments>
            <pubDate>Wed, 14 Sep 2011 05:51:05 +0100</pubDate>
            <guid isPermaLink="false">5228699</guid>        </item>
        <item>
            <title>Central Giant Cell Lesion</title>
            <link>http://www.medworm.com/index.php?rid=5212530&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F53361v01651r0736%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A classic case of central giant cell lesion (CGCL) is presented with emphasis on clinical, radiologic, and histologic features.
 The differential is discussed including peripheral giant cell granuloma, brown tumor of hyperparathyroidism, and giant cell
 tumor of bone. The molecular pathway of osteoclastogenesis is selectively reviewed and applied to suggest possible etiologies
 of the giant cell lesions. CGCL syndromes and treatment are also discussed.
 
 
	Content Type Journal ArticleCategory Sine qua none Radiology-PathologyPages 1-4DOI 10.1007/s12105-011-0297-4Authors
		James C. Valentine, Department of Anatomic Pathology, Naval Medical Center San Diego, 34800 Bob Wilson Drive, San Diego, CA 92134-5000, USABrenda L. Nelson, Department of Anatomic Pathology, Naval Med...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5212530</comments>
            <pubDate>Tue, 06 Sep 2011 15:43:09 +0100</pubDate>
            <guid isPermaLink="false">5212530</guid>        </item>
        <item>
            <title>Elastofibroma Oralis</title>
            <link>http://www.medworm.com/index.php?rid=5198470&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkx27q240x8811wjg%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s12105-011-0299-2Authors
		Thomas Daley, HSA412 Division of Oral Pathology, Department of Pathology, University of Western Ontario, London, ON N6A 5C1, CanadaMark Darling, HSA412 Division of Oral Pathology, Department of Pathology, University of Western Ontario, London, ON N6A 5C1, Canada
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5198470</comments>
            <pubDate>Mon, 05 Sep 2011 16:15:24 +0100</pubDate>
            <guid isPermaLink="false">5198470</guid>        </item>
        <item>
            <title>Muscle Invasion in Oral Tongue Squamous Cell Carcinoma as a Predictor of Nodal Status and Local Recurrence: Just as Effective as Depth of Invasion?</title>
            <link>http://www.medworm.com/index.php?rid=5198471&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy323125865v10368%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tumor depth of invasion (DOI) is a histologic feature that consistently correlates with lymph node metastasis; however, there
 are many difficulties with accurately assessing DOI. The aim of this study was to identify a simpler and more reproducible
 method of determining DOI, by using skeletal muscle invasion as a surrogate marker of depth. Oral tongue squamous cell carcinoma
 American Joint Committee on Cancer (AJCC) stage T1 cases were identified in the Emory University Department of Pathology database.
 61 cases, with a minimum of 2&amp;nbsp;years of follow-up, were included in the study. Cases were examined histologically to assess
 muscle invasion and DOI. The two methods of measurement were analyzed to determine the positive predictive value (PPV) of
 DOI or muscle i...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5198471</comments>
            <pubDate>Sun, 04 Sep 2011 10:54:09 +0100</pubDate>
            <guid isPermaLink="false">5198471</guid>        </item>
        <item>
            <title>Clinical Pathologic Conference Case 6: Infantile Myofibroma</title>
            <link>http://www.medworm.com/index.php?rid=5198472&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff643634m0838u255%2F</link>
            <description>Content Type Journal ArticleCategory American Academy of Oral and Maxillofacial Pathology 65th Annual Meeting, San Juan, Puerto RicoPages 1-4DOI 10.1007/s12105-011-0294-7Authors
		James Rokos, Department of Oral Pathology, Medicine, and Radiology, University of Missouri Kansas City, School of Dentistry, Kansas City, MO, USARomán Carlos, Division of Oral and Maxillofacial Pathology, Centro Clínico de Cabeza y Cuello/Hospital Herrera Llerandi, Guatemala City, GuatemalaMário José Romañach, Oral Pathology Section, Piracicaba Dental School, University of Campinas, Piracicaba, São Paulo, Brazil
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5198472</comments>
            <pubDate>Sun, 04 Sep 2011 10:54:08 +0100</pubDate>
            <guid isPermaLink="false">5198472</guid>        </item>
        <item>
            <title>Clinical Pathologic Conference Case 5: Agranulocytosis</title>
            <link>http://www.medworm.com/index.php?rid=5186284&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj828m42u40422003%2F</link>
            <description>Content Type Journal ArticleCategory American Academy of Oral and Maxillofacial Pathology 65th Annual Meeting, San Juan, Puerto RicoPages 1-6DOI 10.1007/s12105-011-0295-6Authors
		Z. B. Kurago, Oral and Maxillofacial Pathology, Radiology and Medicine, NYU College of Dentistry, New York, NY, USAA. R. Kerr, Oral and Maxillofacial Pathology, Radiology and Medicine, NYU College of Dentistry, New York, NY, USAN. Narayana, UNMC, College of Dentistry, Lincoln, NE, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5186284</comments>
            <pubDate>Wed, 31 Aug 2011 05:52:19 +0100</pubDate>
            <guid isPermaLink="false">5186284</guid>        </item>
        <item>
            <title>Palate Hyperpigmentation Caused by Prolonged Use of the Anti-Malarial Chloroquine</title>
            <link>http://www.medworm.com/index.php?rid=5186285&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F748042nwq075640u%2F</link>
            <description>This report presents a case of palate pigmentation related to the prolonged use of chloroquine diphosphate caused
 by the deposition of drug metabolites in the mucosa. Healthcare professionals must be aware of these drugs and their adverse
 effects in order to make the correct diagnosis, decide on the optimal treatment for the condition, or refer the patient to
 an appropriate specialist.
 
 
	Content Type Journal ArticleCategory Sine qua non Clinicopathologic CorrelatPages 1-3DOI 10.1007/s12105-011-0288-5Authors
		Mário Rodrigues de Melo Filho, Department of Dentistry, State University of Montes Claros, Montes Claros, Minas Gerais, BrazilCélsia Adriane Dias da Silva, DDS, State University of Montes Claros, Unimontes, Montes Claros, Minas Gerais, BrazilMaurício da Rocha Dourado, DDS, St...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5186285</comments>
            <pubDate>Tue, 30 Aug 2011 05:42:40 +0100</pubDate>
            <guid isPermaLink="false">5186285</guid>        </item>
        <item>
            <title>Clinical Pathologic Conference Case 2: Langerhans Cell Histiocytosis</title>
            <link>http://www.medworm.com/index.php?rid=5171682&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7v21rk0064512873%2F</link>
            <description>Content Type Journal ArticleCategory American Academy of Oral and Maxillofacial Pathology 65th Annual Meeting, San Juan, Puerto RicoPages 1-3DOI 10.1007/s12105-011-0290-yAuthors
		John E. Kacher, JKJ Pathology, 4223 Research Forest Dr., Ste 500, The Woodlands, TX 77381, USAElizabeth Philipone, Department of Oral Pathology, Columbia University, 630 W. 168th St, PH15 W-1562, New York, NY 10032, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5171682</comments>
            <pubDate>Sat, 27 Aug 2011 15:47:23 +0100</pubDate>
            <guid isPermaLink="false">5171682</guid>        </item>
        <item>
            <title>Clinical Pathologic Conference Case 4: Hylanizing Clear Cell Carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5149079&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq80lr0730r04q516%2F</link>
            <description>Content Type Journal ArticleCategory American Academy of Oral and Maxillofacial Pathology 65th Annual Meeting, San Juan, Puerto RicoPages 1-5DOI 10.1007/s12105-011-0292-9Authors
		Darren Cox, Department of Pathology and Medicine, Arthur A. Dugoni School of Dentistry, University of the Pacific, San Francisco, CA 94115, USAChristel Haberland, Pediatric Dentistry, Yale-New Haven Hospital, Hamden, CT 06514, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5149079</comments>
            <pubDate>Mon, 22 Aug 2011 15:57:33 +0100</pubDate>
            <guid isPermaLink="false">5149079</guid>        </item>
        <item>
            <title>Clinical Pathologic Conference Case 1: Wegener’s Granulomatosis</title>
            <link>http://www.medworm.com/index.php?rid=5149080&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F07419170n631217k%2F</link>
            <description>Content Type Journal ArticleCategory American Academy of Oral and Maxillofacial Pathology 65th Annual Meeting, San Juan, Puerto RicoPages 1-5DOI 10.1007/s12105-011-0291-xAuthors
		Susan Müller, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA 30322, USASiema Eljack, Hackensack University Medical Center, Hackensack, NJ, USAJohn M. DelGaudio, Department of Otolaryngology Head and Neck Surgery, Emory University School of Medicine, Atlanta, GA 30322, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5149080</comments>
            <pubDate>Mon, 22 Aug 2011 15:57:32 +0100</pubDate>
            <guid isPermaLink="false">5149080</guid>        </item>
        <item>
            <title>Clinical Pathologic Conference Case 3: Nodular Fasciitis</title>
            <link>http://www.medworm.com/index.php?rid=5149081&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpk40225721671018%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intraoral nodular nodular fasciitis is a rare entity that is important to recognize because it may simulate a malignancy clinically
 and histologically. The rapid growth and high mitotic index seen in nodular fasciitis may suggest a malignant neoplastic process,
 but it is generally considered to be a benign reactive proliferation. Recognizing the unique histologic features of nodular
 fasciitis is important to avoid a possible misdiagnosis as a malignancy, leading to unnecessary further treatment.
 
 
	Content Type Journal ArticleCategory American Academy of Oral and Maxillofacial Pathology 65th Annual Meeting, San Juan, Puerto RicoPages 1-5DOI 10.1007/s12105-011-0289-4Authors
		Aparna Naidu, Texas A&amp;M Health Science Center-Baylor College of Dentistry, 3302 Gaston Ave....</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5149081</comments>
            <pubDate>Mon, 22 Aug 2011 15:57:31 +0100</pubDate>
            <guid isPermaLink="false">5149081</guid>        </item>
        <item>
            <title>Branchial Cleft Cyst with Xanthogranulomatous Inflammation</title>
            <link>http://www.medworm.com/index.php?rid=5149082&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F636v233605g73080%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Xanthogranulomatous inflammation (XGI) is a special type of inflammation presenting as mass lesions and mimicking malignant
 tumors. It is rarely described in the head and neck region, and to the best of our knowledge, there are no cases associated
 with branchial cleft cyst. A 39-year-old woman with an infiltrative cystic neck mass that radiologically mimicks a malignant
 tumor is herein presented. The histopathologic diagnosis was a branchial cleft cyst with XGI. XGI may be associated wih branchial
 cleft cysts. Patients may present with radiologic findings mimicking an invasive malignant tumor, and should be taken into
 account during the differential diagnosis with cystic squamous cell carcinoma.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-4DOI 10.1...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5149082</comments>
            <pubDate>Thu, 18 Aug 2011 05:50:36 +0100</pubDate>
            <guid isPermaLink="false">5149082</guid>        </item>
        <item>
            <title>Metastatic Tumors to the Oral Cavity: A Clinical Study of 18 Cases</title>
            <link>http://www.medworm.com/index.php?rid=5081975&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbp8251125t215803%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study was to describe the clinical features of 18 cases of metastatic tumors to the oral cavity. The files
 of patients seen between 1992 and 2009 with oral (soft tissue and jawbones) metastatic lesions were reviewed. Clinical features,
 including gender, age, site of the primary tumor, site of metastatic tumor and treatment were evaluated. Patients were 11
 males and 7 females, with mean age of 64.6&amp;nbsp;years. In males, most primary tumors originated in the lungs. In females, the lung
 and breast were the most common sites of the primary tumors. The mandible was the main site for the development of the metastatic
 lesions and the most common histologic type was adenocarcinoma. Treatment modalities included radiotherapy, chemotherapy and
 surgical resec...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5081975</comments>
            <pubDate>Sat, 30 Jul 2011 15:52:46 +0100</pubDate>
            <guid isPermaLink="false">5081975</guid>        </item>
        <item>
            <title>Expression of p16 in Sinonasal Undifferentiated Carcinoma (SNUC) Without Associated Human Papillomavirus (HPV)</title>
            <link>http://www.medworm.com/index.php?rid=5081976&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2635714813301874%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Sinonasal undifferentiated carcinoma (SNUC) is an uncommon and highly aggressive neoplasm of the paranasal sinuses and nasal
 cavity. Its undifferentiated histologic appearance often requires immunohistochemical studies to distinguish it from other
 high-grade neoplasms. Due to the rarity of SNUC, its immunohistochemical staining profile has been incompletely characterized,
 and little work has been done on its expression of the markers for human papillomavirus (HPV). Our objective is to expand
 our knowledge of its immunophenotype and its association with HPV in order to define markers with mechanistic potential in
 the disease process, or of possible therapeutic importance. A total of five patients (one woman and four men) with SNUC, ranging
 in age from 26 to 75&amp;nbsp...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5081976</comments>
            <pubDate>Fri, 29 Jul 2011 16:06:11 +0100</pubDate>
            <guid isPermaLink="false">5081976</guid>        </item>
        <item>
            <title>Discrimination of ‘Driver’ and ‘Passenger’ HPV in Tonsillar Carcinomas by the Polymerase Chain Reaction, Chromogenic In Situ Hybridization, and p16INK4a Immunohistochemistry</title>
            <link>http://www.medworm.com/index.php?rid=5065420&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa67r732877702703%2F</link>
            <description>This study has compared the polymerase chain reaction (PCR), chromogenic in situ hybridization (CISH), and p16INK4a immunohistochemistry in the assessment of HPV status in TSCC. Archival specimens of TSCC from thirty patients were investigated.
 HPV was detected by PCR in 25/30 (83.3%) tumors; HPV16 (70.0%) and HPV52 (6.7%) were the most common types. HPV was corroborated
 by CISH in 22/25 (88.0%) specimens; integrated HPV was implicated by the presence of punctate signals in each of these cases.
 p16INK4a staining was found in 20/22 (90.9%) HPV PCR positive samples; two PCR/CISH HPV positive cases were p16INK4a negative and two HPV negative samples were p16INK4a positive. These data suggest that a minority of HPV positive TSCCs are positive for passenger HPV and that two or more assays
 m...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5065420</comments>
            <pubDate>Sat, 23 Jul 2011 15:48:11 +0100</pubDate>
            <guid isPermaLink="false">5065420</guid>        </item>
        <item>
            <title>Intravascular Fasciitis: Report of an Intraoral Case and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=5058660&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy4wl05n770374424%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intravascular fasciitis (IF) is an unusual variant of nodular fasciitis. It is characterized by intraluminal, intramural,
 and extramural involvement of small to large arteries or veins. Only three cases involving the oral cavity have been reported
 previously in the literature. Here we present an additional case of oral IF arising in the submucosa of the upper lip of a
 20-year old female. Microscopic examination showed a well-circumscribed, nodular proliferation of spindle cells arranged in
 intersecting fascicles. Occasional multinucleated giants cells also were noted. The tumor was present within the lumen of
 an intermediate-sized artery and extended into adjacent smaller vessels, thereby creating a multinodular appearance. Extramural
 extension into the surroundin...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5058660</comments>
            <pubDate>Thu, 21 Jul 2011 18:04:31 +0100</pubDate>
            <guid isPermaLink="false">5058660</guid>        </item>
        <item>
            <title>Mammary Analogue Secretory Carcinoma: The First Submandibular Case Reported Including Findings on Fine Needle Aspiration Cytology</title>
            <link>http://www.medworm.com/index.php?rid=5058661&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhut864483vk43837%2F</link>
            <description>We present the first case (male, 35&amp;nbsp;years old) of a mammary analogue secretory carcinoma occurring in a submandibular gland
 and document findings on fine needle aspiration cytology. On histology, the tumor displayed characteristic features: circumscribed
 nodules composed of bland, pink to light red neoplastic cells with low proliferative/mitotic activity arranged in tubular,
 vaguely cribriform, and microcystic structures containing Periodic acid Schiff-positive, diastase-resistant secretory material.
 Immunohistochemistry showed strong and diffuse positivity for cytokeratin 7, S100 protein, and vimentin, as well as moderate
 to strong immunoreactivity for c-kit in the majority of tumor cells. A rearrangement of the ETV6 gene on fluorescence in situ hybridization was documented. The...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5058661</comments>
            <pubDate>Wed, 20 Jul 2011 12:28:01 +0100</pubDate>
            <guid isPermaLink="false">5058661</guid>        </item>
        <item>
            <title>Odontogenic Fibroma, Including Amyloid and Ossifying Variants</title>
            <link>http://www.medworm.com/index.php?rid=5032307&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkgt14446102u6622%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Sixty-five cases of odontogenic fibroma (OdonF) are herein presented having been segregated into peripheral, extra bony tumors
 (n&amp;nbsp;=&amp;nbsp;40) and tumors arising in bone or centrally (n&amp;nbsp;=&amp;nbsp;25). All cases were characterized microscopically by a fibrous proliferation
 that varied within and between cases in cellularity and collagen fibril diameter, with intermixed odontogenic epithelial islands
 and cords. All central lesions presented as well demarcated radiolucencies and resorption of contiguous tooth roots was a
 common finding. These intraosseous lesions were of the WHO type; the so-called nonWHO type was excluded as all lesions with
 this diagnosis were devoid of an epithelial component and could be reclassified as other soft tissue fibrogenic tumors. Ne...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5032307</comments>
            <pubDate>Wed, 13 Jul 2011 06:12:28 +0100</pubDate>
            <guid isPermaLink="false">5032307</guid>        </item>
        <item>
            <title>Focal Osseous Dysplasia</title>
            <link>http://www.medworm.com/index.php?rid=5012714&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F35238v8357883222%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Focal osseous dysplasia (FOD) is one of the benign fibro-osseous lesions of the jaw bones and the most commonly occuring benign
 fibro-osseous lesion. This entity occurs more commonly in females and has a predilection for African Americans. Radiographically,
 the lesion has a variable appearance depending on the duration but may appear as a radiolucent to radiopaque lesion that can
 be well to poorly defined. Hisotologically, when biopsied, there are fragments of bony trabeculae intermixed with fibrous
 stroma with incomplete stromal vasculature. The main differential diagnosis is with ossifying fibroma, which is neoplastic
 while FOD is considered a reactive process. Most patients with FOD may be followed clinically without surgical intervention.
 
 
	Content Type Jour...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5012714</comments>
            <pubDate>Sat, 09 Jul 2011 06:19:26 +0100</pubDate>
            <guid isPermaLink="false">5012714</guid>        </item>
        <item>
            <title>Carcinoma ex Pleomorphic Adenoma: A Comprehensive Review of Clinical, Pathological and Molecular Data</title>
            <link>http://www.medworm.com/index.php?rid=5012715&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj1k0434ng5qx53j8%2F</link>
            <description>This study intends to review the literature and highlight
 the current clinical and molecular perspectives about this entity. The most common clinical presentation of CA ex PA is of
 a firm mass in the parotid gland. The proportion of adenoma and carcinoma components determines the macroscopic features of
 this neoplasm. The entity is difficult to diagnose pre-operatively. Pathologic assessment is the gold standard for making
 the diagnosis. Treatment for Ca ex PA often involves an ablative surgical procedure which may be followed by radiotherapy.
 Overall, patients with Ca ex PA have a poor prognosis. Accurate diagnosis and aggressive surgical management of patients presenting
 with Ca ex PA can increase their survival rates. Molecular studies have revealed that the development of Ca ex P...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5012715</comments>
            <pubDate>Sat, 09 Jul 2011 06:19:25 +0100</pubDate>
            <guid isPermaLink="false">5012715</guid>        </item>
        <item>
            <title>Hyalinizing Trabecular Tumor of the Thyroid: A Case Report</title>
            <link>http://www.medworm.com/index.php?rid=4994941&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpv478w77202j7771%2F</link>
            <description>We report
 a case of HTT in a 69-year-old woman with a mutinodular goiter. Since the clinical and ultrasonographic features were nonspecific,
 fine needle aspiration biopsy (FNAB) of the left lobe-dominant node was performed that resulted in an indeterminate cytologic
 diagnosis (category THY-3). The patient underwent total thyroidectomy, with a histologic diagnosis of HTT. We discuss the
 clinical and diagnostic approach, including the role of FNAB, and the pathologic features of HTT with special reference to
 the possible differential diagnosis. Total thyroidectomy or hemithyroidectomy represent adequate treatments, while radioiodine
 ablation is not standard. Although rare cases of malignant HTT have been documented, this tumor should be considered a benign
 neoplasm or, at most, a neop...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4994941</comments>
            <pubDate>Thu, 30 Jun 2011 17:49:02 +0100</pubDate>
            <guid isPermaLink="false">4994941</guid>        </item>
        <item>
            <title>Lymphoepithelial Carcinoma: Two Case Reports and a Systematic Review of Oral and Sinonasal Cases</title>
            <link>http://www.medworm.com/index.php?rid=4963479&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffu11971123044015%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Lymphoepithelial carcinoma (LEC) is a rare malignancy. Histologically, it is an undifferentiated carcinoma with an intermixed
 reactive lymphoplasmacytic infiltrate. Herein, we report two cases of LEC in the head and neck region that presented to Oulu
 University Hospital. Our first case is a 30-year-old man with LEC in the left maxillary sinus. The second case is a 49-year-old
 man with LEC in the soft palate and uvula with regional lymph node metastases at diagnosis. In addition, a systematic review
 of the literature from 1980 to 2010 was performed with MEDLINE and cross-references were searched manually. Case reports and
 clinical series of oral, oropharyngeal, nasal, and paranasal sinus LECs were reviewed revealing a total of 110 cases. Most
 of the oral cases were...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4963479</comments>
            <pubDate>Wed, 22 Jun 2011 15:58:43 +0100</pubDate>
            <guid isPermaLink="false">4963479</guid>        </item>
        <item>
            <title>Chondromyxoid Fibroma of the Ethmoid Sinus</title>
            <link>http://www.medworm.com/index.php?rid=4963481&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv2q18737447q2282%2F</link>
            <description>Content Type Journal ArticlePages 1-4DOI 10.1007/s12105-011-0275-xAuthors
		James T. Castle, Department Of Oral and Maxillofacial Pathology, Naval Postgraduate Dental School, NMMPT&amp;E, Bethesda, MD 20889-5611, USAMikelle L. Kernig, Oral and Maxillofacial Pathology, Wright-Patterson AFB, Dayton, OH 45433, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4963481</comments>
            <pubDate>Tue, 21 Jun 2011 18:33:58 +0100</pubDate>
            <guid isPermaLink="false">4963481</guid>        </item>
        <item>
            <title>Sclerosing Epithelioid Fibrosarcoma of the Oral Cavity</title>
            <link>http://www.medworm.com/index.php?rid=4963480&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5653127w80n80452%2F</link>
            <description>We present an example of a rare FUS-positive SEF that arose in the floor
 of mouth of a 56&amp;nbsp;year old male. Light microscopy, exhaustive immunohistology, and FISH examination showing chromosome rearrangement
 using the FUS break-apart probe led to an erroneous diagnosis of LGFMS with giant collagen rosettes. An outside expert agreed
 with that diagnosis citing the FISH results as confirmatory. Upon review almost 2&amp;nbsp;years later after local recurrence, the
 classic histopathologic features of SEF were noted instead. This example suggests that at least a subset if not most examples
 of SEF are part of the LGFMS “family” of neoplasms, and reiterates the value of careful histologic examination in an age of
 increasingly sophisticated and presumably specific molecular results.
 
 
	Co...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4963480</comments>
            <pubDate>Tue, 21 Jun 2011 18:33:58 +0100</pubDate>
            <guid isPermaLink="false">4963480</guid>        </item>
        <item>
            <title>Oral Elastofibromatous Lesions: A Review and Case Series</title>
            <link>http://www.medworm.com/index.php?rid=4948009&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F644j201103366183%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Elastofibromas of the oral cavity are rare, with only 5 cases reported. In this paper, we present a series of five new cases
 of oral elastofibromatous lesions, occurring in 4 males and 1 female, with ages ranging from 33 to 76&amp;nbsp;years. The clinical
 differential diagnosis includes fibroepithelial polyp or fibroma, among other connective tissue tumours. Elastofibromas probably
 develop as reactive lesions, for which surgical treatment is definitive.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s12105-011-0274-yAuthors
		Mark R. Darling, Division of Oral Pathology, Department of Pathology, University of Western Ontario, London, ON N6A 5C1, CanadaMaciej Kutalowski, Division of Oral Pathology, Department of Pathology, University of Western Ontario, London, ON N...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4948009</comments>
            <pubDate>Fri, 17 Jun 2011 12:02:15 +0100</pubDate>
            <guid isPermaLink="false">4948009</guid>        </item>
        <item>
            <title>An Unexpected Finding of a Bronchogenic Cyst Presenting as a Thyroid Mass</title>
            <link>http://www.medworm.com/index.php?rid=4948008&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe6005865m4357312%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Herein we present a case of a bronchogenic cyst masquerading as a thyroid mass. Bronchogenic cysts are rare congenital malformations
 that result from an abnormal development of the ventral foregut during organogenesis. They are commonly asymptomatic lesions
 rarely found in the neck. In our case, a young male presented with complaints of neck discomfort over a long period presumed
 to be secondary to a thyroid mass based on imaging studies. Fine needle aspiration was inconclusive. Post-operative pathological
 sectioning revealed evidence of a bronchogenic cyst. These lesions have a low incidence of malignancy, and complete surgical
 excision has been recommended.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s12105-011-0272-0Authors
		Alagappan Annamalai, New Y...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4948008</comments>
            <pubDate>Fri, 17 Jun 2011 12:02:15 +0100</pubDate>
            <guid isPermaLink="false">4948008</guid>        </item>
        <item>
            <title>Salivary Oncocytic Cystadenoma with Intraluminal Crystalloids: a Case Report with Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4948007&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F700k53g374234r02%2F</link>
            <description>We report a case of 53-year-old man with a progressively enlarging lump in the left submandibular
 region. Ultrasound examination revealed a cystic mass with an intraluminal fluid collection. The tumor was surgically removed.
 Histologic examination yielded a diagnosis of oncocytic cystadenoma with a high concentration of intraluminal crystalloids.
 The microscopic features of the crystalloids were compatible with nontyrosine (alpha-amylase) crystalloids. When compared
 with previously published cases in the literature, this is the first report of oncocytic cystadenoma with intraluminal crystalloids
 arising in the submandibular gland, and the second reported case of the nontyrosine type of crystalloids occurring in association
 with this tumor. The nontyrosine crystalloids may be highly c...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4948007</comments>
            <pubDate>Fri, 17 Jun 2011 12:02:15 +0100</pubDate>
            <guid isPermaLink="false">4948007</guid>        </item>
        <item>
            <title>The Role of RANK/RANKL/OPG Signalling Pathways in Osteoclastogenesis in Odontogenic Keratocysts, Radicular Cysts, and Ameloblastomas</title>
            <link>http://www.medworm.com/index.php?rid=4916095&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F163m87w2127166t3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study was to evaluate the immunohistochemical expression of molecules involved in osteoclastogenesis, including
 the receptor activator of nuclear factor kappa B (RANK), RANK ligand (RANKL) and osteoprotegerin (OPG) in odontogenic keratocysts
 (OKCs), which has been named as a keratocystic odontogenic tumour by the WHO, and compare their expression with radicular
 cysts and ameloblastomas. RANK is a member of tumour necrosis factor receptor family and it is activated by RANK ligand. OPG
 binds to RANKL and inactivates it. The imbalance of these factors could cause the differential bone resorption activity in
 some diseases and tumours. The expression of these molecules was evaluated in ameloblastomas (n&amp;nbsp;=&amp;nbsp;20), OKCs (n&amp;nbsp;=&amp;nbsp;20), and radic...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916095</comments>
            <pubDate>Sun, 05 Jun 2011 05:46:32 +0100</pubDate>
            <guid isPermaLink="false">4916095</guid>        </item>
        <item>
            <title>Carcinoma Cuniculatum Arising in the Tongue</title>
            <link>http://www.medworm.com/index.php?rid=4916096&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl031n5tl117q561v%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Carcinoma cuniculatum (CC) is a rare, distinct clinico-pathological variant of squamous cell carcinoma (SCC) that is defined
 histologically by the characteristic infiltrative pattern of a deep, broad, and complex proliferation of stratified squamous
 epithelium with keratin cores and keratin-filled crypts. Herein, we present a case report of CC of the oral tongue and discuss
 its diagnosis, management, and outcome, as well as briefly review the world literature. To our knowledge, this is the first
 documented case of CC of the tongue to be reported in the English literature. We draw attention to its clinico-pathological
 features and highlight that awareness of this entity as a distinct variant of SCC facilitates its correct management.
 
 
	Content Type Journal Articl...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916096</comments>
            <pubDate>Sat, 04 Jun 2011 05:53:17 +0100</pubDate>
            <guid isPermaLink="false">4916096</guid>        </item>
        <item>
            <title>Perivascular Epithelioid Cell Tumors (PEComas) of the Head and Neck: Report of Three Cases and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4897443&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr250102702vw54l6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;PEComas are a family of neoplastic lesions that share overlapping morphology, immunohistochemistry, and ultrastructure that
 include angiomyolipoma, lymphangioleiomyomatosis, clear cell “sugar” tumor of the lung as well as similar tumors occurring
 in a variety of visceral, cutaneous and soft tissue sites throughout the body. The defining histopathological features are
 epithelioid cells with a perivascular distribution containing clear to pale eosinophilic granular cytoplasm and a round-to-oval
 centrally located nucleus with an inconspicuous nucleolus. Immunohistochemically, coexpression of melanocytic (HMB-45 and/or
 Melan-A) and myoid markers are characteristic. In the present study, we describe three PEComas occurring in the head and neck
 (nasal cavity and lar...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4897443</comments>
            <pubDate>Mon, 30 May 2011 17:02:11 +0100</pubDate>
            <guid isPermaLink="false">4897443</guid>        </item>
        <item>
            <title>Seromucinous Hamartoma of the Nasal Cavity: A Report of Two Cases and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4897444&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frl39705v7uq8t726%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The sinonasal tract is a complex anatomic site, home to a wide variety of reactive, inflammatory, benign, and malignant lesions.
 Inflammatory polyps and papillomas are usually easily recognized by pathologists. A poorly understood lesion that has been
 more clearly defined in recent years is the nasal hamartoma. The epithelial subtypes include seromucinous hamartoma, respiratory
 epithelial adenomatoid hamartoma, and hybrid lesions. Seromucinous hamartomas have only been recognized and substantially
 reported over the past few years. They are a diagnostic challenge, needing to be distinguished from low grade adenocarcinomas,
 and are of interest because most of the basic questions about their pathophysiology remain unanswered. Herein, we present
 two novel cases of ser...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4897444</comments>
            <pubDate>Thu, 26 May 2011 16:09:13 +0100</pubDate>
            <guid isPermaLink="false">4897444</guid>        </item>
        <item>
            <title>Metastatic Pulmonary Adenocarcinoma Deposit Arising Within a Cutaneous Basal Cell Carcinoma: A Case Report</title>
            <link>http://www.medworm.com/index.php?rid=4849266&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv637p841p3631533%2F</link>
            <description>We report our experience
 of a solitary pulmonary adenocarcinoma metastasis that arose within a pre-existing basal cell carcinoma in a patient with
 undiagnosed lung cancer. Immunohistochemistry was invaluable in confirming both the metastatic nature of the secondary skin
 lesion and its site of origin.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s12105-011-0263-1Authors
		Elinor Carey, Royal Gwent Hospital, Newport, Wales, UKSimon D. Jones, ABM University NHS Trust, Morriston Hospital, Swansea, Wales, UKPaul Griffiths, ABM University NHS Trust, Morriston Hospital, Swansea, Wales, UKPrue Baxter, ABM University NHS Trust, Morriston Hospital, Swansea, Wales, UK
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4849266</comments>
            <pubDate>Thu, 19 May 2011 16:35:01 +0100</pubDate>
            <guid isPermaLink="false">4849266</guid>        </item>
        <item>
            <title>Pseudotumor of the Mandible as First Presentation of Hemophilia in a 2-Year-Old Male: A Case Report and Review of Jaw Pseudotumors of Hemophilia</title>
            <link>http://www.medworm.com/index.php?rid=4834837&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F014ut0632265343w%2F</link>
            <description>We present a case in a two-year-old male with a one-month swelling of the right mandible without
 significant medical history or diagnosis of hemophilia who was subsequently diagnosed as having Factor IX deficiency, or hemophilia
 B. A review of the literature revealed only 15 reported cases of PTH of the jaws and salient features of PTH in the jaws are
 discussed. The differential diagnosis of masses occurring in the jaws of children is limited and PTH should be considered
 when a mass presents with rapid growth and the histopathologic features are not diagnostic for a neoplastic process, even
 in the absence of a prior diagnosis of hemophilia as PTH may be the initial manifestation of this disease.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s12105-011-0267-xAuthors
		D. P. Cox...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4834837</comments>
            <pubDate>Thu, 12 May 2011 16:45:06 +0100</pubDate>
            <guid isPermaLink="false">4834837</guid>        </item>
        <item>
            <title>Unique presentation of adenoid cystic carcinoma in postcricoid region: a case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=4823806&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3u7r32256rx559l1%2F</link>
            <description>We present a case of adenoid cystic carcinoma of the larynx arising in the inter-arytenoid
 and postcricoid region in a 54-year-old woman. To our knowledge, this is the first case of adenoid cystic carcinoma arising
 in this particular region of the larynx.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s12105-011-0266-yAuthors
		Ozlem Saraydaroglu, Department of Pathology, Uludag University Medical School, 16059 Bursa, TurkeyHakan Coskun, Department of Otorhinolaryngology and Head-Neck Surgery, Uludag University Medical School, Bursa, TurkeyMehtap Kasap, Department of Pathology, Uludag University Medical School, 16059 Bursa, Turkey
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4823806</comments>
            <pubDate>Wed, 11 May 2011 05:51:28 +0100</pubDate>
            <guid isPermaLink="false">4823806</guid>        </item>
        <item>
            <title>Tenascin-C in Chronic Sclerosing Sialadenitis</title>
            <link>http://www.medworm.com/index.php?rid=4823805&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb8763n2403484g50%2F</link>
            <description>This study was undertaken to expand our understanding of the processes involved in fibrosis
 that occurs in chronic sclerosing sialadenitis (CSS) by investigating the distribution of tenascin-C. Fifteen specimens of
 CSS with varying degrees of fibrosis and five normal submandibular glands were retrospectively examined immunohistochemically
 for the distribution of TNC. Linear deposition of TNC was found around collecting ducts in normal glands and around collecting
 ducts without surrounding fibrotic tissue in CSS; percentage incidences were not statistically different. In contrast, broader,
 band-like deposition of TNC was found in the fibrous tissue around collecting ducts in CSS with widespread degree of fibrosis
 compared to little or no fibrosis; the percentage incidence was statisti...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4823805</comments>
            <pubDate>Wed, 11 May 2011 05:51:28 +0100</pubDate>
            <guid isPermaLink="false">4823805</guid>        </item>
        <item>
            <title>Pseudotumor of the Tracheal-Laryngeal Junction with Unusual Morphologic Features Caused by Rhodococcus equi Infection</title>
            <link>http://www.medworm.com/index.php?rid=4769091&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1344875284403183%2F</link>
            <description>In this report, we review the literature
 of these unusual lesions and compare them to cases of conventional malakoplakia involving the large airways. We also explore
 the pathogenetic mechanisms that may contribute to the distinctive histologic appearance of Rhodococcus-associated pseudotumors.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s12105-011-0259-xAuthors
		Shreeram Akilesh, Department of Pathology and Immunology, Barnes-Jewish Hospital, St. Louis, MO 63110, USASara Cross, Department of Internal Medicine, Division of Infectious Diseases, Barnes-Jewish Hospital, St. Louis, MO 63110, USAKatherine Kimmelshue, Department of Pathology and Immunology, Barnes-Jewish Hospital, St. Louis, MO 63110, USANigar Kirmani, Department of Internal Medicine, Division of Infectious Diseases,...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4769091</comments>
            <pubDate>Mon, 25 Apr 2011 16:43:25 +0100</pubDate>
            <guid isPermaLink="false">4769091</guid>        </item>
        <item>
            <title>Orbital Infantile Myofibroma: a Case Report and Clinicopathologic Review of 24 Cases from the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4750059&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyl655488105l732h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Isolated orbital infantile myofibroma are rare tumors in the head and neck. The mass-like clinical presentation and variable
 histologic features result in frequent misdiagnosis and potentially inappropriate clinical management. There are only a few
 reported cases in the English literature. Twenty-four patients with orbital infantile myofibroma or myofibromatosis were compiled
 from the English literature (Medline 1960–2011) and integrated with this case report. The patients included 14 males and 10
 females, aged newborn to 10&amp;nbsp;years (mean, 34.8&amp;nbsp;months), who presented with a painless mass in the infra- or supraorbital regions,
 usually increasing in size andassociated with exophthalmos (n&amp;nbsp;=&amp;nbsp;5). Females were on average older than their male counter...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4750059</comments>
            <pubDate>Thu, 21 Apr 2011 18:01:26 +0100</pubDate>
            <guid isPermaLink="false">4750059</guid>        </item>
        <item>
            <title>Oral Squamous Cell Carcinoma with Mandibular Bone Invasion: Intraoperative Evaluation of Bone Margins by Routine Frozen Section</title>
            <link>http://www.medworm.com/index.php?rid=4750058&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy25970531qx87462%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The intraoperative knowledge of margin status on mandibulectomy specimens is important for primary reconstruction. The goal
 of this study was to evaluate whether intraoperative bone marrow (BM) curettings and inferior alveolar nerve (IAN) biopsies
 are representative of final decalcified cross-sectional (shave) mandibular bone margins. Forty-seven margins in 27 patients
 consecutively treated with segmental mandibulectomy for squamous cell carcinoma were reviewed. These patients had BM or IAN
 margins sampled by surgeons and assessed intraoperatively by routine frozen section. The full cross-section of mandibular
 bone margins were sampled by pathologists at the time of routine gross examination. Intraoperative evaluation of BM/IAN biopsies
 is characterized by a 50% s...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4750058</comments>
            <pubDate>Thu, 21 Apr 2011 18:01:26 +0100</pubDate>
            <guid isPermaLink="false">4750058</guid>        </item>
        <item>
            <title>Carcinoma ex Pleomorphic Adenoma of the Nasal Cavity</title>
            <link>http://www.medworm.com/index.php?rid=4745540&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F51m1746773g2u274%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Carcinomatous transformation of a PA in the nasal cavity is extremely rare, but does occur. Accordingly, PAs of this site
 should be thoroughly sampled and closely examined to exclude the possibility of malignant transformation.
 
 
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s12105-011-0262-2Authors
		Ashley Cimino-Mathews, Department of Pathology, The Johns Hopkins Medical Institutions, 600N. Wolfe St., Pathology Building 401, Baltimore, MD 21287, USABrian M. Lin, School of Medicine, The Johns Hopkins Medical Institutions, Baltimore, MD, USASteven S. Chang, Department of Facial Plastic and Reconstructive Surgery, The Johns Hopkins Medical Institutions, Baltimore, MD, USAKofi D. Boahene, Department of Facial Plastic and Reconstructive Surgery, The Johns Ho...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4745540</comments>
            <pubDate>Wed, 20 Apr 2011 06:08:17 +0100</pubDate>
            <guid isPermaLink="false">4745540</guid>        </item>
        <item>
            <title>Cemento-Osseous Dysplasia-Like Lesion and Complex Odontoma Associated with an Impacted Third Molar</title>
            <link>http://www.medworm.com/index.php?rid=4745539&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd30707744m831617%2F</link>
            <description>We present a case of a 36-year-old female with a benign fibro-osseous lesion consistent with cemento-osseous dysplasia (COD)
 that was located coronally to the crown of an impacted mandibular third molar tooth and was associated with a complex odontoma.
 The pathogenesis of this unusual association is discussed and the odontogenic origin of COD is suggested.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s12105-011-0261-3Authors
		Georgios I. Prodromidis, Department of Oral Pathology, Faculty of Dentistry, National and Kapodistrian University of Athens, Athens, GreeceKonstantinos I. Tosios, Department of Oral Pathology, Faculty of Dentistry, National and Kapodistrian University of Athens, Athens, GreeceIoannis G. Koutlas, Division of Oral Pathology, School of Dentistry, University o...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4745539</comments>
            <pubDate>Wed, 20 Apr 2011 06:08:17 +0100</pubDate>
            <guid isPermaLink="false">4745539</guid>        </item>
        <item>
            <title>Intraductal Carcinoma of Salivary Gland (So-Called Low-Grade Cribriform Cystadenocarcinoma) Arising in an Intraparotid Lymph Node</title>
            <link>http://www.medworm.com/index.php?rid=4647239&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4n45l4v00224j58n%2F</link>
            <description>This report describes, for the first time, an entirely intranodal location for a low-grade intraductal carcinoma (so-called
 low-grade cribriform cystadenocarcinoma).
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s12105-011-0256-0Authors
		Ilan Weinreb, Department of Pathology, University Health Network and Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON M5G 2C4, Canada
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4647239</comments>
            <pubDate>Fri, 25 Mar 2011 18:52:20 +0100</pubDate>
            <guid isPermaLink="false">4647239</guid>        </item>
        <item>
            <title>EBV-Positive Plasmacytoma of the Submandibular Gland—Report of a Rare Case with Molecular Genetic Characterization</title>
            <link>http://www.medworm.com/index.php?rid=4647240&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk18183j7688g17h8%2F</link>
            <description>We describe a case of an EBV-positive plasmacytoma presenting as a 7.7&amp;nbsp;cm submandibular
 mass in an elderly immunocompetent man which displayed an abundance of “naked nuclei” on fine needle aspiration cytology.
 The tumor showed lambda light chain restriction and positive expression for CD38, MUM1 and EBER. Subsequent investigation
 for myeloma revealed absence of M-protein and end-organ damage, except for a lytic lesion in the radial bone. An extensive
 fluorescent in situ hybridization analysis showed the tumor to be negative for the t(4;14) FGFR3/IGH translocation as well as translocations involving the IGH,
 IGL, IGK, CCND1, BCL2, BCL6 and C-MYC genes. KRAS genetic analysis did not reveal any mutations of codons 12, 13 and 61.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4647240</comments>
            <pubDate>Fri, 25 Mar 2011 18:52:16 +0100</pubDate>
            <guid isPermaLink="false">4647240</guid>        </item>
        <item>
            <title>Biphasic Low-Grade Nasopharyngeal Papillary Adenocarcinoma with a Prominent Spindle Cell Component: Report of a Case Localized to the Posterior Nasal Septum</title>
            <link>http://www.medworm.com/index.php?rid=4618269&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn785148p83141978%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A case (female, 39&amp;nbsp;years of) of thyroid-like nasopharyngeal low-grade papillary adenocarcinoma with a significant spindle
 cell component is presented. The tumor was located on the posterior nasal septum. The spindle cells displayed nuclear features
 very much similar to the epithelial component and the two cell types merged imperceptibly. Immunohistochemically, the neoplastic
 cells (including the spindle cell component) were strongly and diffusely positive for TTF-1, cytokeratins (AE1-3), cytokeratin
 19 and vimentin. C-kit immunohistochemistry showed diffuse mild to moderate membranous positivity with focal areas displaying
 moderate to strong immunoreactivity. EMA was strongly positive in the epithelial component with membranous and cytoplasmic
 reactivity wher...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4618269</comments>
            <pubDate>Sat, 19 Mar 2011 16:56:49 +0100</pubDate>
            <guid isPermaLink="false">4618269</guid>        </item>
        <item>
            <title>Lack of Correlation Between Microvascular Density and Pathological Features and Outcomes in Sinonasal and Oral Mucosal Melanomas</title>
            <link>http://www.medworm.com/index.php?rid=4618271&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy068mm65415271u5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Unlike its cutaneous counterpart, prognostic markers for primary mucosal malignant melanoma have not been well elucidated.
 It has been recently demonstrated that microvascular density (MVD) in cutaneous malignant melanoma has a significant negative
 correlation with survival; however, this has not been well-studied in mucosal malignant melanoma of the head and neck. This
 study explores the potential association between MVD, various histological parameters, and the outcome of a series of sinonasal
 and oral mucosal melanomas. Nineteen such cases were immunostained with CD31 and the MVD was calculated by using Bioquant
 Image Analysis Software (R and M Biometrics, Nashville, TN). These cases included 16 sinonasal and 3 oral cavity tumors. The
 1, 2, 3, 4 and 5&amp;nbsp;year...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4618271</comments>
            <pubDate>Sat, 19 Mar 2011 02:52:49 +0100</pubDate>
            <guid isPermaLink="false">4618271</guid>        </item>
        <item>
            <title>Solitary Fibrous Tumor with Entrapment of Minor Salivary Gland Tissue: An Unusual Presentation That Requires Exclusion of Pleomorphic Adenoma</title>
            <link>http://www.medworm.com/index.php?rid=4618270&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyhn1768232r627l5%2F</link>
            <description>We report two unusual cases of solitary fibrous tumor (SFT) of minor salivary glands that microscopically mimicked pleomorphic
 adenoma. One of these lesions presented in the retromolar region and the other in the buccal mucosa. The microscopic features
 of these two tumors and their intimate relationship with regional mucous minor salivary glands posed a diagnostic challenge.
 Awareness of the morphological diversity of SFT coupled to a judicious use of appropriate immunohistochemical probes should
 prove valuable to accurately segregate SFT from pleomorphic adenoma.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s12105-011-0254-2Authors
		Jose Luis Tapia, Department of Oral Diagnostic Sciences, School of Dental Medicine, University at Buffalo, 3435 Main Street, 355 Squire Hall, Bu...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4618270</comments>
            <pubDate>Sat, 19 Mar 2011 02:52:49 +0100</pubDate>
            <guid isPermaLink="false">4618270</guid>        </item>
        <item>
            <title>Development and Growth of Adenomatoid Odontogenic Tumor Related to Formation and Eruption of Teeth</title>
            <link>http://www.medworm.com/index.php?rid=4562842&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy2329517v2826q47%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The number of published cases of adenomatoid odontogenic tumor (AOT) has steadily increased, and about half were reported
 in Asian populations. Although the clinicopathologic profile of AOT has been extensively reported, factual knowledge of its
 pathogenesis is rudimentary at best, and there is controversy as to precisely which odontogenic epithelium it arises from.
 AOT is a successional tooth-associated lesion which develops during the mixed dentition. The permanent successor differs from
 its deciduous predecessor in that it has an eruptive pathway from the dental follicle to the gingiva, the gubernaculum dentis.
 With this background in mind, the present review focuses mainly on the early development of AOT. We successfully demonstrated
 a close spatial relationsh...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4562842</comments>
            <pubDate>Sat, 05 Mar 2011 16:51:00 +0100</pubDate>
            <guid isPermaLink="false">4562842</guid>        </item>
        <item>
            <title>Localized Tongue Amyloidosis in a Patient with Neurofibromatosis Type II</title>
            <link>http://www.medworm.com/index.php?rid=4509102&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe22301j1526774g2%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;This case highlights the possibility of oral manifestations as the only sign of AL and reveals the unexpected co-existence
 of AL and NF 2, for the first time.
 
 
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s12105-011-0251-5Authors
		Dimitrios Andreadis, Department of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki, 54124 Thessaloniki, GreeceAthanasios Poulopoulos, Department of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki, 54124 Thessaloniki, GreecePetros Papadopoulos, Department of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki, 54124 Thessaloniki, GreeceApostolos Epivatianos, Department of Oral Medicine/Pathology, School of Dentistry, Aristotle Un...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4509102</comments>
            <pubDate>Mon, 21 Feb 2011 17:08:42 +0100</pubDate>
            <guid isPermaLink="false">4509102</guid>        </item>
        <item>
            <title>Orofacial Granulomatosis: A Clinicopathologic Correlation</title>
            <link>http://www.medworm.com/index.php?rid=4491713&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F12xh7k0v1517n533%2F</link>
            <description>We report one such case of a female patient who presented with a persistent upper
 lip enlargement. She had visited multiple general dental practitioners and general physicians but was undiagnosed. Ultrasonography
 proved an adjunctive tool in diagnosis. She was treated with a combination of topical and intra-lesional steroids. A 1&amp;nbsp;year
 follow-up did not show any evidence of recurrence.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s12105-011-0249-zAuthors
		Titus K. Thomas, Department of Oral and Maxillofacial Surgery, Meenakshi Ammal Dental College &amp; Hospital, Alapakkam Main Road, Maduravoyal, Chennai, IndiaR. S. Neelakandan, Department of Oral and Maxillofacial Surgery, Meenakshi Ammal Dental College &amp; Hospital, Alapakkam Main Road, Maduravoyal, Chennai, IndiaDarpan Bharga...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4491713</comments>
            <pubDate>Wed, 16 Feb 2011 07:00:13 +0100</pubDate>
            <guid isPermaLink="false">4491713</guid>        </item>
        <item>
            <title>Myocbacterium-Avium Intracellulare Associated Inflammatory Pseudotumor of the Anterior Nasal Cavity</title>
            <link>http://www.medworm.com/index.php?rid=4491715&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F030581345t8p48pm%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In this case report, we describe an unusual case of mycobacterial associated inflammatory pseudotumor that occurred in a patient
 with a previous history of cocaine abuse. We discuss inflammatory pseudotumor (IPT) in general and emphasize the rare entity
 where an associated mycobacterial infection is seen. The histogenesis is not yet completely understood. The lesion can pose
 challenges for practicing pathologists and a misdiagnosis of malignancy can occur at multiple facets. A discussion about the
 differential diagnosis and clues to make the distinction is presented. In addition to spindle cell proliferation, the presence
 of a background of mixed inflammatory cell infiltrate and foamy macrophages are clues to make the diagnosis. In the case of
 mycobacteria associa...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4491715</comments>
            <pubDate>Wed, 16 Feb 2011 07:00:11 +0100</pubDate>
            <guid isPermaLink="false">4491715</guid>        </item>
        <item>
            <title>Calcifying Epithelial Odontogenic Tumor (Pindborg Tumor)</title>
            <link>http://www.medworm.com/index.php?rid=4491714&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F843831u184x8h369%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The calcifying epithelial odontogenic tumor is a benign epithelial tumor with characteristic clinical and histopathologic
 features. These features are discussed with a typical case presentation along with emphasis on newer variants and management
 strategies.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s12105-011-0250-6Authors
		Punnya V. Angadi, Department of Oral Pathology and Microbiology, KLEVK Institute of Dental Sciences and Hospital, Belgaum, 590010 Karnataka IndiaK. Rekha, Department of Oral Pathology and Microbiology, S.D.M College of Dental Sciences and Hospital, Dharwad, 580009 Karnataka India
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4491714</comments>
            <pubDate>Wed, 16 Feb 2011 07:00:11 +0100</pubDate>
            <guid isPermaLink="false">4491714</guid>        </item>
        <item>
            <title>Lymphocytic Host Response to Oral Squamous Cell Carcinoma: An Adaptive T-Cell Response at the Tumor Interface</title>
            <link>http://www.medworm.com/index.php?rid=4485824&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft613hr4712043123%2F</link>
            <description>In this study, we test the hypothesis that strong LHR corresponds to a greater degree of adaptive cytotoxic T
 cell response as compared to moderate LHR. We studied resection specimens of primary oral squamous carcinoma classified as
 having either strong (n&amp;nbsp;=&amp;nbsp;16), intermediate (n&amp;nbsp;=&amp;nbsp;20) or weak (n&amp;nbsp;=&amp;nbsp;4) LHR. CD20+, CD4+, &amp; CD8+ cells were detected by immunohistochemistry
 and quantified at 40× with a grid; counting the 10 fields with the most lymphocytes at the tumor interface and within tumors.
 Mean counts/tumor were analyzed by the 2-sided T-test. Statistically significant differences were observed for interface CD8 cells with respect to strong versus moderate LHR, strong versus weak LHR, and moderate versus weak LHR, and tumor infiltrating
 CD8 cells with ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4485824</comments>
            <pubDate>Mon, 14 Feb 2011 07:09:56 +0100</pubDate>
            <guid isPermaLink="false">4485824</guid>        </item>
        <item>
            <title>Adenosquamous Carcinoma of the Head and Neck: Relationship to Human Papillomavirus and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4461657&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg53351061712335h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Adenosquamous carcinoma (ADSC) of the head and neck is an aggressive variant of squamous cell carcinoma (SCC). Certain variants
 of head and neck SCC are human papillomavirus (HPV)-related and have better prognosis. The relationship of HPV to head and
 neck ADSC has not been investigated. We searched our files for the term “adenosquamous” and head and neck subsites and found
 cases from 1998 to 2009. The requisite histologic criteria were the presence of SCC combined with distinct gland formation
 and/or intracellular mucin. DNA in situ hybridization for high-risk HPV, RNA in situ hybridization for high risk HPV E6 and
 E7 transcripts, and immunohistochemistry for p16 and p53 were performed. The existing literature on ADSC was also reviewed.
 Of the 18 cases, eight ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4461657</comments>
            <pubDate>Tue, 08 Feb 2011 21:31:05 +0100</pubDate>
            <guid isPermaLink="false">4461657</guid>        </item>
        <item>
            <title>Oral Verruciform Xanthoma Associated with Chronic Graft-Versus- Host Disease: A Report of Five Cases and a Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4461658&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F84k43527021274j1%2F</link>
            <description>We report of a series
 of five cases with VX who concurrently had chronic oral graft-versus-host disease following hematopoietic stem cell transplantation.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s12105-011-0246-2Authors
		Shokoufeh Shahrabi Farahani, Harvard School of Dental Medicine, 49 Worthington Street #7, Boston, MA 02120, USANathaniel S. Treister, Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Boston, MA USAZainab Khan, Harvard School of Dental Medicine, Boston, MA USASook-Bin Woo, Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Boston, MA USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4461658</comments>
            <pubDate>Tue, 08 Feb 2011 21:31:03 +0100</pubDate>
            <guid isPermaLink="false">4461658</guid>        </item>
        <item>
            <title>Clear Cell Carcinoma and Clear Cell Odontogenic Carcinoma: a Comparative Clinicopathologic and Immunohistochemical Study</title>
            <link>http://www.medworm.com/index.php?rid=4440059&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp854087521236746%2F</link>
            <description>In this study the clinicopathologic, histologic,
 and immunohistochemical features of 17 CCCs and 12 CCOCs are examined. The differential diagnosis of clear cell malignancies
 in the head and neck is discussed. The relationship of CCCs and CCOCs to other clear cell tumors on the basis of their immunohistochemical
 staining patterns is postulated.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s12105-011-0244-4Authors
		Elizabeth A. Bilodeau, Department of Diagnostic Sciences, University of Pittsburgh School of Dental Medicine, 3501 Terrace St, Pittsburgh, PA 15261, USAAaron P. Hoschar, Department of Pathology, The Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44106, USAE. Leon Barnes, Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA USAJennifer ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4440059</comments>
            <pubDate>Thu, 03 Feb 2011 21:13:03 +0100</pubDate>
            <guid isPermaLink="false">4440059</guid>        </item>
        <item>
            <title>Selected Topics on Lymphoid Lesions in the Head and Neck Regions</title>
            <link>http://www.medworm.com/index.php?rid=4440060&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F788621xk1x643875%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Lymphoid tissue located in the head and neck region include multiple regional lymph node chains as well as mucosa associated
 lymphoid tissue of the conjunctiva, buccal and nasopharyngeal cavities (Waldeyer’s ring), and thyroid and salivary glands.
 This region is a rich source of antigenic stimuli including infectious agents coming from the outside environment. Many reactive
 conditions that affect lymphoid tissue in this region may mimic neoplasia. In fact, distinguishing between benign and malignant
 lymphoid proliferations in the head and neck region is a relatively frequent diagnostic challenge and in many instances, this
 distinction is not straightforward. It therefore behooves the practicing pathologist to be able to recognize the benign lymphoproliferative
 d...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4440060</comments>
            <pubDate>Thu, 03 Feb 2011 21:12:54 +0100</pubDate>
            <guid isPermaLink="false">4440060</guid>        </item>
        <item>
            <title>Sclerosing Polycystic Adenosis of the Parotid Gland: Report of a Bifocal, Paucicystic Variant with Ductal Carcinoma in situ and Pronounced Stromal Distortion Mimicking Invasive Carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=4440061&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F22mj6637614247u8%2F</link>
            <description>We present a case (female patient, age 45&amp;nbsp;years) with a bifocal, paucicystic variant of sclerosing polycystic adenosis of
 the parotid gland with cribriform ductal carcinoma in situ (DCIS) and pronounced stromal distortion affecting the in situ
 component to such an extent that it gave a distinct impression of intralesional invasive adenocarcinoma. P63–and calponin-positive
 myoepithelial cells were present in the periphery of the acini and ducts in the benign component, somewhat discontinuously
 in the DCIS-component, and even in the periphery of the small irregular atypical cell nests that appeared infiltrative on
 the haematoxylin and eosin stained sections. Strong cytoplasmic immunoreactivity for GCDFP-15 was detected in the benign component
 with a variable, patchy and mostly w...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4440061</comments>
            <pubDate>Tue, 01 Feb 2011 08:40:54 +0100</pubDate>
            <guid isPermaLink="false">4440061</guid>        </item>
        <item>
            <title>Angiomyxolipoma (Vascular Myxolipoma) of the Oral Cavity. Report of a Case and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4440062&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr62228136767jlmh%2F</link>
            <description>We describe the clinical and histopathologic findings of the first case of intraoral
 angiomyxolipoma in a 12&amp;nbsp;year-old male, as well as the utility of immunohistochemistry as a useful tool in differential diagnosis
 of this particular lesion with respect to other benign and malignant lesions derived from adipose tissue.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s12105-011-0241-7Authors
		Guillermo Martínez-Mata, Faculty of Dentistry, Universidad Autónoma de Chihuahua, Chihuahua, MéxicoMendoza-Farías Rocío, Oral and Maxillofacial Surgery Service, Hospital Juárez de México, Mexico City, DF, MéxicoLicéaga-Escalera Carlos Juan, Oral and Maxillofacial Surgery Service, Hospital Juárez de México, Mexico City, DF, MéxicoAlmeida Oslei Paes, Faculty of Dentistry, Univers...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4440062</comments>
            <pubDate>Tue, 01 Feb 2011 08:40:53 +0100</pubDate>
            <guid isPermaLink="false">4440062</guid>        </item>
        <item>
            <title>Synchronous Squamous Cell Carcinoma of Tongue and Unicentric Cervical Castleman’s Disease Clinically Mimicking a Stage IV Disease: A Rare Association or Coincidence?</title>
            <link>http://www.medworm.com/index.php?rid=4379523&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyt26625864jx64n2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Malignancy in a setting of hyaline vascular type of Castleman’s disease (HVCD) is an exceptional occurrence. Herein, we report
 an extremely rare case of synchronous unicentric cervical HVCD and squamous cell carcinoma (SCC) of tongue mimicking stage
 IV disease. A 32-year-old gentleman presented with an ulcerated mass on the right tongue border and ipsilateral cervical nodal
 mass. As the clinical stage was IVB (T1N3M0), an anterior two-third glossectomy with bilateral modified neck dissection was performed. On gross examination, an ulcerated
 mass on the right lateral border was identified. In addition, an 8&amp;nbsp;cm large nodal mass at right level III–V was seen. Microscopy
 from the ulcerated growth in the tongue revealed an invasive well differentiated squamous ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4379523</comments>
            <pubDate>Mon, 17 Jan 2011 20:41:35 +0100</pubDate>
            <guid isPermaLink="false">4379523</guid>        </item>
        <item>
            <title>Oral Manifestations of Dermatologic Disease: A Focus on Lichenoid Lesions</title>
            <link>http://www.medworm.com/index.php?rid=4339917&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9p35821522x3x07g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Lichenoid changes in the oral mucosa can be encountered in a wide range of lesions with varied etiologies including immune-mediated
 disorders, reactions to systemic medications and to dental materials. Dysplasia of the oral cavity can exhibit a lichenoid
 histology, which may mask the potentially cancerous component. Another unusual clinical disease, proliferative verrucous leukoplakia,
 can often mimic oral lichen planus clinically requiring careful correlation of the clinical and pathologic features.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s12105-010-0237-8Authors
		Susan Müller, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, 1364 Clifton Road NE, Atlanta, GA 30322, USA
	

	
		Journal Head and Neck PathologyOnline...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4339917</comments>
            <pubDate>Mon, 10 Jan 2011 15:55:01 +0100</pubDate>
            <guid isPermaLink="false">4339917</guid>        </item>
        <item>
            <title>Papillary Thyroid Carcinoma Variants</title>
            <link>http://www.medworm.com/index.php?rid=4328174&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg010884022p55up3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Papillary thyroid carcinomas are the most common thyroid cancers and constitute more than 70% of thyroid malignancies. The
 most common etiologic factor is radiation, but genetic susceptibility and other factors also contribute to the development
 of papillary thyroid carcinoma. The most common variants include conventional, follicular variant and tall cell variant. However,
 many other uncommon variants have been described including oncocytic, columnar cell, diffuse sclerosing and solid forms. Immunohistochemical
 staining with TTF-1 and thyroglobulin is very useful in confirming the diagnosis of papillary thyroid carcinoma especially
 in metastatic sites. Markers such as HBME-1 and CITED1 can assist in separating some difficult cases of follicular variants
 of papilla...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4328174</comments>
            <pubDate>Fri, 07 Jan 2011 14:52:04 +0100</pubDate>
            <guid isPermaLink="false">4328174</guid>        </item>
        <item>
            <title>A Review of NUT Midline Carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=4328175&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6q763q2222r6022l%2F</link>
            <description>This article reviews the clinicopathologic features of these malignancies. Ancillary
 testing is discussed as well as the pathologic differential diagnosis.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s12105-010-0235-xAuthors
		Edward B. Stelow, Dept of Pathology, UVA Health System, University of Virginia, Jefferson Park Ave., Box 800214, Charlottesville, VA 22908, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4328175</comments>
            <pubDate>Fri, 07 Jan 2011 14:51:59 +0100</pubDate>
            <guid isPermaLink="false">4328175</guid>        </item>
        <item>
            <title>Desmoplastic Fibroblastoma (Collagenous Fibroma): A Case Identified in the Buccal Mucosa</title>
            <link>http://www.medworm.com/index.php?rid=4328177&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd4714225n3312x8x%2F</link>
            <description>This article presents a case report of a
 56-year-old man, with no previous history of trauma, who presented a slow-growing mass in the buccal mucosa. Histopathology
 and immunohistochemistry staining studies were performed, and a diagnosis of the desmoplastic fibroblastoma was made. The
 patient has been disease-free for one year.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s12105-010-0239-6Authors
		Sílvia Ferreira de Sousa, Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais BrazilPatrícia Carlos Caldeira, Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais BrazilSoraya de Mattos Camargo Grossmann, Department of Oral Surg...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4328177</comments>
            <pubDate>Fri, 07 Jan 2011 14:51:58 +0100</pubDate>
            <guid isPermaLink="false">4328177</guid>        </item>
        <item>
            <title>A Rare Case of Dentigerous Cyst in a One Year Old Child: The Earliest Known Reported Occurrence</title>
            <link>http://www.medworm.com/index.php?rid=4328176&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm1k4223t07719323%2F</link>
            <description>This article describes a rare case of dentigerous
 cyst in a 1-year-old boy, the youngest case to be documented. The clinical, radiographic and histopathologic features are
 discussed; the increased possibility of occurrence of these cysts at a very young age and the importance of timely diagnosis
 of such cysts to avoid future complications is emphasized.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s12105-010-0238-7Authors
		Rakesh Suresh, Department of Oral Pathology and Microbiology, Amrita School of Dentistry, Kochi, 682041 Kerala IndiaMahija Janardhanan, Department of Oral Pathology and Microbiology, Amrita School of Dentistry, Kochi, 682041 Kerala IndiaAnna P. Joseph, Department of Oral Pathology and Microbiology, Amrita School of Dentistry, Kochi, 682041 Kerala IndiaR. B. ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4328176</comments>
            <pubDate>Fri, 07 Jan 2011 14:51:58 +0100</pubDate>
            <guid isPermaLink="false">4328176</guid>        </item>
        <item>
            <title>Aggressive Osteoblastoma of the Maxilla: A Case Report and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4288068&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl8m542187716t0u6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Aggressive osteoblastoma is a rare primary bone neoplasm with the potential for local invasion and recurrence. While the vertebrae
 or long bones are most commonly affected, few well-documented cases have been reported in the jaws. A 25-year-old man presented
 with a palatal mass of several months’ duration. He reported the lesion had undergone gradual enlargement and, while generally
 asymptomatic, had recently become increasingly painful. An incisional biopsy was interpreted as “osteoblastic neoplasm” most
 suggestive of osteoblastoma. However, final diagnosis was deferred until the resection specimen could be evaluated. Following
 partial maxillectomy, histopathologic examination revealed a proliferation of large epithelioid cells with eccentric nuclei
 and pro...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4288068</comments>
            <pubDate>Wed, 22 Dec 2010 22:44:20 +0100</pubDate>
            <guid isPermaLink="false">4288068</guid>        </item>
        <item>
            <title>Not Your Usual Cancer Case: Variants of Laryngeal Squamous Cell Carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=4273766&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp612620773885632%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although squamous cell carcinoma (SCC) variants account for less than 10% of all laryngeal SCCs, they have many unique biological,
 morphological, and clinical features. They are also easily confused with other tumor types. Recognition of them is critical
 for surgical pathologists as is the knowledge of what they mean for the patient. Three of the most common and important of
 these are basaloid, verrucous, and papillary SCC. These tumor types will be briefly reviewed with a focus on specific controversies,
 biological questions, and/or recent advancements in our understanding of them.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0232-0Authors
		James S. Lewis, Department of Pathology and Immunology, Division of Anatomic and Molecular Pathology, Washington U...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4273766</comments>
            <pubDate>Thu, 16 Dec 2010 18:27:27 +0100</pubDate>
            <guid isPermaLink="false">4273766</guid>        </item>
        <item>
            <title>Paradental (Mandibular Inflammatory Buccal) Cyst</title>
            <link>http://www.medworm.com/index.php?rid=4269256&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp222415kn6g061v5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The paradental cyst is commonly misinterpreted when associated with atypical clinical and radiographic characteristics, in
 turn causing diagnostic problems. For this reason, the study of the differential diagnosis of this lesion has become extremely
 important. In addition, the correlation of clinical, histologic, and radiographic findings are also of great value in obtaining
 accurate diagnoses. The minor variations in the clinical appearance of paradental cysts make it feasible to consider the two
 main groups of cysts separately: those associated with 1st and 2nd permanent molars of the mandible and those associated with
 the 3rd mandibular molar. Moreover, this distinction in localization may well dictate the necessary treatment. Bearing in
 mind the minor clinical...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4269256</comments>
            <pubDate>Wed, 15 Dec 2010 16:05:50 +0100</pubDate>
            <guid isPermaLink="false">4269256</guid>        </item>
        <item>
            <title>Lymphangioma of the Vallecula</title>
            <link>http://www.medworm.com/index.php?rid=4239745&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp62m111532807205%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s12105-010-0230-2Authors
		James T. Castle, Department Of Oral &amp; Maxillofacial Pathology, Naval Postgraduate Dental School, NMMPT&amp;E, 8901 Wisconsin Ave., Bethesda, MD 20889-5611, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4239745</comments>
            <pubDate>Mon, 06 Dec 2010 15:09:07 +0100</pubDate>
            <guid isPermaLink="false">4239745</guid>        </item>
        <item>
            <title>Plasmacytoid Myoepithelioma of the Palate: Case Report</title>
            <link>http://www.medworm.com/index.php?rid=4239746&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff23730155702q4l3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Myoepitheliomas are extremely rare benign neoplasms of salivary glands. They represent 1–1.5% of all salivary gland tumors.
 They occur, principally, in the parotid gland and infrequently in minor salivary glands. There are distinct histological and
 immunohistochemical characteristics of the tumor which aid in the diagnosis. Myoepithelioma of the palate is uncommon and
 only a limited number of cases has been reported in the English literature. Herein, a case of plasmacytoid type of myoepithelioma
 of the palate in an adult female is presented along with review of the literature.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0231-1Authors
		Matina T. Zormpa, Department of Oral Medicine and Maxillofacial Pathology, School of Dentistry, Aristotle University o...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4239746</comments>
            <pubDate>Mon, 06 Dec 2010 15:09:06 +0100</pubDate>
            <guid isPermaLink="false">4239746</guid>        </item>
        <item>
            <title>Small Lymphocytic Lymphoma Obscuring Microscopic Tonsillar Squamous Cell Carcinoma: an Unknown Occurrence with a Known Primary</title>
            <link>http://www.medworm.com/index.php?rid=4227354&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx4w3046p5v425827%2F</link>
            <description>We report herein a rare occurrence of tonsillar
 involvement by small lymphocytic lymphoma (SLL) incidentally detected during the workup for a cervical lymph node SCC metastasis
 of a 52-year-old non-smoker male. The microscopic human papillomavirus-positive SCC involving the tonsillar surface and crypts
 was obscured by SLL leading to the initial designation of ‘unknown primary’. The occult HNSCC are likely explained by small
 tumor size, quality and quantity of sampling, thoroughness of endoscopic, radiological and pathological assessment or a combination
 of the above. The coexistence of another tumor such as lymphoma has not yet been reported as a confounding factor in the workup
 for cervical SCC metastasis. Since oropharyngeal SCC can be very small and Waldeyer’s ring is a comm...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4227354</comments>
            <pubDate>Tue, 30 Nov 2010 17:55:36 +0100</pubDate>
            <guid isPermaLink="false">4227354</guid>        </item>
        <item>
            <title>Unusual Benign Smooth Muscle Lesions of the Tongue: Review and Report of Two Cases</title>
            <link>http://www.medworm.com/index.php?rid=4227355&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl439834t11m46714%2F</link>
            <description>We present two cases of benign smooth muscle proliferations
 in the tongue, provide a review, briefly discuss histogenesis and offer a clinico-pathological differential diagnosis.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0229-8Authors
		M. R. Darling, DSB 4015, Division of Oral Pathology, Department of Pathology, Schulich School of Medicine and Dentistry, University of Western Ontario, 1151 Richmond Street, London, ON N6A 5C1, CanadaB. Wehrli, Department of Pathology, Schulich School of Medicine and Dentistry, University of Western Ontario, 1151 Richmond Street, London, ON N6A 5C1, CanadaE. Zeligman, Argyle Associates, 239 Argyle Avenue, Ottawa, ON K2P 1B8, CanadaJ. Smillie, Dental Practice, 323 Wilson Street E #201, Ancaster, ON L9G 4A8, CanadaT. Daley, DSB 4015, Division o...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4227355</comments>
            <pubDate>Tue, 30 Nov 2010 08:17:19 +0100</pubDate>
            <guid isPermaLink="false">4227355</guid>        </item>
        <item>
            <title>Ewing’s Family of Tumors of the Sinonasal Tract and Maxillary Bone</title>
            <link>http://www.medworm.com/index.php?rid=4206666&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyx0510x86w76w484%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Ewing’s family of tumors (EFT) are malignant neoplasms affecting children and young adults. Most cases arise in the long
 bones or the pelvis. Primary EFT of head and neck is uncommon and primary sinonasal EFT is even rarer. Previous studies have
 not focused on the sinonasal region specifically, and the published literature on sinonasal EFT consists of sporadic case
 reports. Fourteen cases of sinonasal EFT were available and had H&amp;Es for review and immunohistochemical stains for CD99, S100,
 keratins, synaptophysin and desmin. FISH or RT-PCR was performed for EWSR1 abnormalities on 8 cases. The 14 identified patients
 included 5 males and 9 females, ranging from 7–70&amp;nbsp;years of age (mean 32.4&amp;nbsp;years). Tumors involved nasal cavity (5), sinuses
 (5) or bo...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4206666</comments>
            <pubDate>Wed, 24 Nov 2010 20:23:57 +0100</pubDate>
            <guid isPermaLink="false">4206666</guid>        </item>
        <item>
            <title>Clinico-Pathologic Conference: Case 6</title>
            <link>http://www.medworm.com/index.php?rid=4201746&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkn3152611175g823%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s12105-010-0221-3Authors
		David Booth, School of Dentistry, University of Western Australia, 17 Monash Avenue, Nedlands, 6009 AustraliaJerry Bouquot, Department of Diagnostic Sciences, University of Texas Dental Branch at Houston, 6516 M.D. Anderson Blvd., Suite 3.094b, Houston, TX 77030, USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4201746</comments>
            <pubDate>Tue, 23 Nov 2010 18:17:11 +0100</pubDate>
            <guid isPermaLink="false">4201746</guid>        </item>
        <item>
            <title>Anaplastic Myoepithelial Carcinoma of the Sinonasal Tract: an Underrecognized Salivary-Type Tumor Among the Sinonasal Small Round Blue Cell Malignancies? Report of One Case and a Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4193906&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcl63g44831512735%2F</link>
            <description>We present a 45&amp;nbsp;year old female patient with a nasal carcinoma showing high-grade/anaplastic histomorphological features and
 with a distinct myoepithelial immunohistochemical phenotype including positivity for smooth muscle actin, p63, S100 protein
 with no sustentacular pattern, calponin, cytokeratin 14, vimentin and cytokeratins (AE1-3 and CK5/6). A minority (&amp;lt;5%) of
 the cells showed focal and variable immunoreactivity for EMA with no cuticular/canalicular pattern. Bcl-2, CD99, CD117 and
 CD56 were variously positive, but chromogranin and synaptophysin were negative. Weak to moderate nuclear p53 immunoreactivity
 was seen in 50% of tumor cells. Mib-1/Ki-67 showed an average proliferation of 60–70%. Fluorescent in situ hybridization revealed
 no EWS-gene translocation. In situ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4193906</comments>
            <pubDate>Sat, 20 Nov 2010 17:52:50 +0100</pubDate>
            <guid isPermaLink="false">4193906</guid>        </item>
        <item>
            <title>Clinico-Pathologic Conference: Case 4</title>
            <link>http://www.medworm.com/index.php?rid=4187775&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbk05041024k14gj2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 13-month-old Japanese boy presented with painless swelling in a left mandible and cheek. Intraoral examination revealed
 swelling in the left mandible and hemorrhage of oral mucosa due to biting. CT images revealed a wide osteolytic lesion of
 the left mandible with floating teeth. Biopsy was carried out and histopathological diagnosis was discussed.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0224-0Authors
		Takashi Muramatsu, Department of Pathology, Tokyo Dental College, 1-2-2, Masago, Mihama-ku, Chiba, 261-8502 JapanGillian L. Hall, Department of Histopathology, Manchester Royal Infirmary, Manchester, UKSadamitsu Hashimoto, Department of Pathology, Tokyo Dental College, 1-2-2, Masago, Mihama-ku, Chiba, 261-8502 JapanJun Miyauchi, Department of Patholog...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4187775</comments>
            <pubDate>Thu, 18 Nov 2010 17:57:00 +0100</pubDate>
            <guid isPermaLink="false">4187775</guid>        </item>
        <item>
            <title>Clinico-Pathologic Conference: Case 5</title>
            <link>http://www.medworm.com/index.php?rid=4187777&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjq2q32144475077w%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s12105-010-0223-1Authors
		Hye-Jung Yoon, Department of Oral Pathology, School of Dentistry, Seoul National University, Seoul, South KoreaPrimali Jayasooriya, Department of Oral Pathology, Faculty of Dental Sciences, University of Peradeniya, Peradeniya, Sri LankaSeong-Doo Hong, Department of Oral Pathology, School of Dentistry, Seoul National University, Seoul, South KoreaJae-Il Lee, Department of Oral Pathology, School of Dentistry, Seoul National University, Seoul, South KoreaSam-Pyo Hong, Department of Oral Pathology, School of Dentistry, Seoul National University, Seoul, South Korea
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4187777</comments>
            <pubDate>Thu, 18 Nov 2010 17:56:59 +0100</pubDate>
            <guid isPermaLink="false">4187777</guid>        </item>
        <item>
            <title>Clinico-Pathologic Conference: Case 3</title>
            <link>http://www.medworm.com/index.php?rid=4187776&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj071852006261764%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s12105-010-0225-zAuthors
		Patricia Devilliers, Department of Anatomic Pathology, University of Alabama at Birmingham, 3656 North Pavilion, 1802 6th Avenue South, Birmingham, AL 35249, USAAnna A. Talacko, Dorevitch Pathology, Melbourne, VIC AustraliaMichael J. Aldred, Dorevitch Pathology, Melbourne, VIC AustraliaJoel K. Cure, Department of Radiology, University of Alabama at Birmingham, Birmingham, AL USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4187776</comments>
            <pubDate>Thu, 18 Nov 2010 17:56:59 +0100</pubDate>
            <guid isPermaLink="false">4187776</guid>        </item>
        <item>
            <title>Metastatic Adenocarcinoma of the Colon: Early Manifestation in Gingival Tissue</title>
            <link>http://www.medworm.com/index.php?rid=4177025&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe525w21126087x88%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A case of gingival metastasis of adenocarcinoma of the colon is reported, the lesion being an early clinical indication of
 a primary malignant tumor. The diagnosis of metastatic lesion in the oral region is always challenging, both to clinician
 and to the pathologist, due to its rarity and complexity. In the present case, the clinical hypothesis was peripheral ossifying
 fibroma or pyogenic granuloma. Histologically, the biopsy tissue revealed a malignant neoplasm not connected to the mucosal
 surface. Immunohistochemically, the lesion was positive for 35ßH11 and cytokeratin 20 and focally positive for cytokeratin
 7. Treatment involved excision of primary tumor and follow-up chemotherapy. The clinical, histological and immunohistochemical
 characteristics are discus...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4177025</comments>
            <pubDate>Mon, 15 Nov 2010 18:08:19 +0100</pubDate>
            <guid isPermaLink="false">4177025</guid>        </item>
        <item>
            <title>Clinico-Pathologic Conference: Case 2</title>
            <link>http://www.medworm.com/index.php?rid=4177026&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx28q4161362q463l%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s12105-010-0220-4Authors
		Camilla Kragelund, Department of Oral Medicine, Section of Oral Pathology, School of Dentistry, University of Copenhagen, 20, Norre Allé, 2200 Copenhagen N, DenmarkShabnum Meer, Division of Oral Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South AfricaLars Pallesen, Department of Oral and Maxillofacial Surgery, School of Dentistry, University of Copenhagen, Copenhagen, DenmarkJesper Reibel, Department of Oral Medicine, Section of Oral Pathology, School of Dentistry, University of Copenhagen, 20, Norre Allé, 2200 Copenhagen N, Denmark
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4177026</comments>
            <pubDate>Sat, 13 Nov 2010 06:47:52 +0100</pubDate>
            <guid isPermaLink="false">4177026</guid>        </item>
        <item>
            <title>Clinico-Pathologic Conference: Case 1</title>
            <link>http://www.medworm.com/index.php?rid=4177027&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F676803845044v324%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s12105-010-0219-xAuthors
		Márcio Ajudarte Lopes, Áreas de Semiologia e Patologia Oral, Departamento de Diagnóstico Oral, Faculdade de Odontologia de Piracicaba, Universidade Estadual de Campinas (UNICAMP), Av. Limeira 901, CP52, Areião, Piracicaba, São Paulo 13414-903, BrazilHyun Sil Kim, Department of Oral Pathology, Oral Cancer Research Institute, College of Dentistry Yonsei University, Seoul, KoreaFernanda Viviane Mariano, Áreas de Semiologia e Patologia Oral, Departamento de Diagnóstico Oral, Faculdade de Odontologia de Piracicaba, Universidade Estadual de Campinas (UNICAMP), Av. Limeira 901, CP52, Areião, Piracicaba, São Paulo 13414-903, BrazilMarcelo Brum Corrêa, Department of Head and Neck Surgery, Oncology Center, Piracicaba, Bra...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4177027</comments>
            <pubDate>Sat, 13 Nov 2010 06:47:51 +0100</pubDate>
            <guid isPermaLink="false">4177027</guid>        </item>
        <item>
            <title>Odontogenic Epithelium: Immunolabeling of Ki-67, EGFR and Survivin in Pericoronal Follicles, Dentigerous Cysts and Keratocystic Odontogenic Tumors</title>
            <link>http://www.medworm.com/index.php?rid=4141650&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn28118852360r715%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study was to evaluate the biological profile of odontogenic epithelium by immunolabeling of epidermal growth
 factor receptor (EGFR), Ki-67 and survivin in keratocystic odontogenic tumors (KOT), dentigerous cysts (DC), and pericoronal
 follicles (PF). Immunohistochemical analysis was performed in 13 KOTs, 14 DCs and 9 PFs. Immunolabeling was analyzed in the
 basal and suprabasal layers of KOTs and DCs, and in the islands of odontogenic epithelium and/or reduced enamel epithelium
 of PFs. KOTs showed the highest proliferation rate among the three groups, mainly in suprabasal layers. EGFR immunolabeling
 was observed mainly in the cytoplasm in basal and suprabasal layers of KOTs and in the suprabasal layer of DCs. Immunolabeling
 in both membrane and cytop...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141650</comments>
            <pubDate>Thu, 04 Nov 2010 17:51:54 +0100</pubDate>
            <guid isPermaLink="false">4141650</guid>        </item>
        <item>
            <title>Erratum to: Inter-observer Agreement in Laryngeal Pre-neoplastic Lesions</title>
            <link>http://www.medworm.com/index.php?rid=4141649&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn4v2773064236200%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s12105-010-0215-1Authors
		Sulen Sarioglu, Department of Pathology, Dokuz Eylul University Faculty of Medicine, 35340 Inciralti, Izmir, TurkeyFulya Cakalagaoglu, Department of Pathology, Yesilyurt Ataturk Research and Education Hospital, Izmir, TurkeySahande Elagoz, Department of Pathology, Cumhuriyet University Faculty of Medicine, Sivas, TurkeyUnsal Han, Department of Pathology, Ankara Diskapi Research and Education Hospital, Ankara, TurkeyDemet Etit, Department of Pathology, Yesilyurt Ataturk Research and Education Hospital, Izmir, TurkeySema Hucumenoglu, Department of Pathology, Ankara Diskapi Research and Education Hospital, Ankara, TurkeyIlgin Karaman, Department of Pathology, Dokuz Eylul University Faculty of Medicine, 35340 Inciralti, Izmir...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4141649</comments>
            <pubDate>Thu, 04 Nov 2010 17:51:54 +0100</pubDate>
            <guid isPermaLink="false">4141649</guid>        </item>
        <item>
            <title>The Spectrum of Gnathic Osteosarcoma: Caveats for the Clinician and the Pathologist</title>
            <link>http://www.medworm.com/index.php?rid=4136860&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9k8361642812j466%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Seven expansile jaw lesions in patients ranging from 7 to 63&amp;nbsp;years are presented to illustrate diagnostic and management issues
 pertaining to cases ultimately proven to be gnathic osteosarcoma (GO). Six of the cases in our series were low-grade osteoblastic
 and one high-grade chondroblastic. None of our cases exhibited the characteristic “sunburst” radiopaque appearance described
 for GO. All of our cases displayed cortical expansion and one showed development of diastema. Two occurred in the maxilla
 and five in the mandible. Two of the patients with mandibular lesions presented initially with pain; all other patients were
 asymptomatic. Lack of pain resulted in a delay in diagnosis due to postponement of consultation or biopsy. Two cases underwent
 initial ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4136860</comments>
            <pubDate>Tue, 02 Nov 2010 17:34:52 +0100</pubDate>
            <guid isPermaLink="false">4136860</guid>        </item>
        <item>
            <title>Uncommon Foreign Body Reactions Occurring in the Lip: Clinical Misdiagnosis and the Use of Special Techniques of Analysis</title>
            <link>http://www.medworm.com/index.php?rid=4136861&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg0u7m22273857406%2F</link>
            <description>This study reports three interesting cases of nodular submucosal lip lesions where foreign-body reactions of unknown origin
 were detected on hematoxylin and eosin (H&amp;E) analysis. These materials were evaluated under polarized light microscopy, scanning
 electron microscopy and by energy dispersive X-ray analysis. The results revealed the following materials: an interdental
 toothbrush bristle, silica, and iron. Unusual mucosal foreign body reaction cases have been reported, but few publications
 used special techniques to identify the specific foreign material. Clinicians and pathologists might consider these techniques
 for identifying the precise origin of these foreign bodies.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0217-zAuthors
		Adriele Ferreira Gouvêa, Department o...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4136861</comments>
            <pubDate>Tue, 02 Nov 2010 17:34:49 +0100</pubDate>
            <guid isPermaLink="false">4136861</guid>        </item>
        <item>
            <title>Sphenoid Sinus Basaloid Squamous Cell Carcinoma Presenting as a Sellar Mass: Report a Case with Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4112970&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq375876h056r18p2%2F</link>
            <description>In this report, we present a case of a female patient
 with a sphenoid sinus mass. Clinically, the patient had progressively decreasing vision and headache. Magnetic resonance imaging
 (MRI) and computerized tomographic (CT) scan showed an infiltrating tumor mass involving the sphenoid sinus and the sella
 with compression of the optic nerve. Pathologic examination revealed an invasive basaloid epithelial neoplasm that was arranged
 in lobules, nests and cords. The tumor also showed palisading of peripheral cells, focal abrupt squamous differentiation and
 in situ carcinoma in the surface mucosa. In the immunohistochemical studies, this tumor revealed a strongly positive nuclear
 staining for p63. The morphologic and ancillary studies indicated a BSCC. To the best of our knowledge, this is...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4112970</comments>
            <pubDate>Sat, 23 Oct 2010 15:49:11 +0100</pubDate>
            <guid isPermaLink="false">4112970</guid>        </item>
        <item>
            <title>Trabecular and Psammomatoid Juvenile Ossifying Fibroma of the Skull Base Mimicking Psammomatoid Meningioma</title>
            <link>http://www.medworm.com/index.php?rid=4092329&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9x15036228282118%2F</link>
            <description>We report a case of a 15-year-old boy who developed progressive proptosis and hypertelorism and was found to have a mid-face
 and skull base tumor, initially diagnosed as psammomatoid meningioma. The tumor recurred and the resected specimen revealed
 a unique OF having trabecular and psammomatoid features. The clinical, radiographic, histopathologic findings and differential
 diagnoses of the case are presented.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0212-4Authors
		Olga L. Bohn, Department of Pathology, MetroHealth Medical Center-Case Western Reserve University, Cleveland, OH 44109, USAJohn R. Kalmar, Section of Oral and Maxillofacial Pathology, College of Dentistry, The Ohio State University Medical Center, Columbus, OH 43210, USACarl M. Allen, Section of Oral and Maxill...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4092329</comments>
            <pubDate>Sat, 16 Oct 2010 08:54:35 +0100</pubDate>
            <guid isPermaLink="false">4092329</guid>        </item>
        <item>
            <title>Peripheral Calcifying Odontogenic Cyst: A Case Report and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=4092328&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr156601t73v60344%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The peripheral calcifying odontogenic cyst (PCOC) accounts for less than 25% of the cases of calcifying odontogenic cysts
 and most commonly appears as a nodule on the gingiva. This paper aims to present both a case report of a PCOC located in the
 left vestibular maxilla as well as a review of the English-language literature. An 11-year-old female patient presented a
 swelling in the vestibular region of teeth 12 and 13. Periapical and panoramic radiographs demonstrated irregular calcification.
 Surgical excision was performed. Microscopic examination showed an odontogenic cystic lesion lined by ameloblastoma-like epithelium,
 containing numerous ghost cells. Areas of calcification associated with ghost cells could also be observed. The patient was
 diagnosed with PCOC...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4092328</comments>
            <pubDate>Sat, 16 Oct 2010 08:54:35 +0100</pubDate>
            <guid isPermaLink="false">4092328</guid>        </item>
        <item>
            <title>Angiosarcoma of the Oral Cavity</title>
            <link>http://www.medworm.com/index.php?rid=4042739&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6lg05475811234q2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Angiosarcoma of the oral cavity is extremely rare. A 54-year-old woman consulted to our hospital because of mass of the left
 cheek next to the mandible. MRI showed a 1&amp;nbsp;cm tumor. Enucleation of the tumor was performed. Grossly, the tumor was not encapsulated
 and had a central cavity. Histologically, the tumor consisted of spindle and polygonal cells with hyperchromatic nuclei with
 nucleoli. Intracytoplasmic vacuoles and mitotic figure were scattered. Vasoformative channels were present in some areas.
 Lymphoid follicles were scattered in the tumor. The tumor was invasive into the surrounding tissue, and lymphovascular permeation
 was noted. The surgical margins were positive. Immunohistochemically, the tumor cells were positive for factor VIII-related
 antigen, C...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4042739</comments>
            <pubDate>Tue, 05 Oct 2010 18:09:50 +0100</pubDate>
            <guid isPermaLink="false">4042739</guid>        </item>
        <item>
            <title>Analysis of Immunohistochemical Expression of K19 in Oral Epithelial Dysplasia and Oral Squamous Cell Carcinoma Using Color Deconvolution-Image Analysis Method</title>
            <link>http://www.medworm.com/index.php?rid=4024603&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv66314x626ju3r3q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;K19 is an intermediate filament protein that has been investigated in oral squamous cell carcinoma (OSCC), but that has not
 been correlated with the amount of keratin produced within well-differentiated OSCC grade. The aim of the present study was
 to objectively analyze K19 immunoexpression in OSCC and to validate the utility of K19 in differentiation among grades of
 oral epithelial dysplasia (OED). Formalin-fixed tissues of 36 primary OSCC (22 well, 10 moderately, 4 poorly differentiated),
 43 OED (23 mild, 8 moderate, 12 severe), and 11 normal oral epithelium (NOE) were included. K19 was immunostained using HRP-DAB
 method. The percentage of K19-positive area was found using color deconvolution program in ImageJ® image analysis system (public domain software, Nati...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4024603</comments>
            <pubDate>Thu, 30 Sep 2010 08:00:48 +0100</pubDate>
            <guid isPermaLink="false">4024603</guid>        </item>
        <item>
            <title>Ectopic Thyroid Presenting as a Submandibular Mass</title>
            <link>http://www.medworm.com/index.php?rid=3996264&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr3458632h43x034p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although extremely rare, the presence of ectopic thyroid tissue in the submandibular region should be considered in the differential
 diagnosis of tissue masses in the cervical region. Diagnosis is confirmed by fine-needle aspiration biopsy and exclusion of
 malignancy should be confirmed by histopathologic analysis of the lesion. In general, surgery is the treatment of choice.
 A rare case of ectopic thyroid in the right submandibular region is reported; it was diagnosed after total thyroidectomy and
 successfully treated through surgery.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0209-zAuthors
		Joseli Assem Bersaneti, Department of Surgery, School of Medical Sciences, Universidade de Marília (UNIMAR), Av. Rio Branco, 1132–Cj. 41, Marília, São Paulo ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3996264</comments>
            <pubDate>Tue, 21 Sep 2010 04:11:00 +0100</pubDate>
            <guid isPermaLink="false">3996264</guid>        </item>
        <item>
            <title>Inter-observer Agreement in Laryngeal Pre-neoplastic Lesions</title>
            <link>http://www.medworm.com/index.php?rid=3996265&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq12248505281kkg2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In this series, laryngeal preneoplastic lesions were evaluated by the classifications of the World Health Organization (WHOC),
 Ljubljana (LC) and squamous intraepithelial neoplasia (SINC) by multiple observers. The inter-observer agreement (IA) by WHOC
 for laryngeal lesions had been previously evaluated, but to the best of our knowledge, there are no data for LC and SINC.
 H&amp;E stained slides from 42 laryngeal biopsies were evaluated by fourteen participants according to WHOC and LC, and SINC was
 additionally applied by 6. The results were analyzed statistically. The diagnoses which were favored by most participants
 for each case, according to WHOC, were as follows: squamous cell hyperplasia (n&amp;nbsp;=&amp;nbsp;5; 12%), mild dysplasia (n&amp;nbsp;=&amp;nbsp;11; 26.2%), moderate d...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3996265</comments>
            <pubDate>Tue, 21 Sep 2010 04:10:57 +0100</pubDate>
            <guid isPermaLink="false">3996265</guid>        </item>
        <item>
            <title>Nasal Sinus Leiomyosarcoma in a Patient with History of Non-Hereditary Unilateral Treated Retinoblastoma</title>
            <link>http://www.medworm.com/index.php?rid=3918107&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjm6w28732r067775%2F</link>
            <description>We report a case of LMS of the nasal sinus area in a 35-year-old African American male with a history
 of non-hereditary unilateral RB and radiation therapy. To the best of our knowledge, this is the first reported case of sinonasal
 LMS arising in a patient with a history of non-hereditary unilateral RB. The clinical history, radiology, and pathology are
 presented along with a brief discussion of the literature.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0207-1Authors
		Sarah G. Fitzpatrick, Department of Oral and Maxillofacial Diagnostic Sciences, University of Florida College of Dentistry, 1600 SW Archer Drive Rm D8-6, Gainesville, FL 32610, USABradford A. Woodworth, Department of Surgery/Division of Otolaryngology, University of Alabama, Birmingham, AL USACarmela Monteiro...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3918107</comments>
            <pubDate>Sat, 28 Aug 2010 17:06:30 +0100</pubDate>
            <guid isPermaLink="false">3918107</guid>        </item>
        <item>
            <title>Case Report: a Pediatric Case of Cementoblastoma with Histologic and Radiographic Features of an Osteoblastoma and Osteosarcoma</title>
            <link>http://www.medworm.com/index.php?rid=3905709&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv8015r1346044146%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;One case of an expansile mass involving the roots of a mandibular left first molar in a nine year old male is presented. The
 lesion has features of a cementoblastoma (CB), osteoblastoma (OB), and osteosarcoma (OS) both radiographically and histologically.
 Radiographically, a “sunburst” appearance is present. Histologically, the lesional tissue is intimately involved with the
 root, not the periosteum. The clinical, radiographic, and histopathologic characteristics of CB, OB, and OS are discussed
 as well as the difficulties associated with distinguishing between these lesions in the gnathic region.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0205-3Authors
		Elizabeth Bilodeau, Department of Diagnostic Sciences, University of Pittsburgh School of Dental...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3905709</comments>
            <pubDate>Wed, 25 Aug 2010 06:14:26 +0100</pubDate>
            <guid isPermaLink="false">3905709</guid>        </item>
        <item>
            <title>B Lymphoblastic Lymphoma Presenting as a Tumor of the Nasopharynx in an Adult Patient</title>
            <link>http://www.medworm.com/index.php?rid=3897856&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2822212831mhu6q4%2F</link>
            <description>We report the case of a 28-year-old male diagnosed
 with a B lymphoblastic lymphoma (CD20−; CD79a+; CD3−; CD10+; PAX5+, CyclinD1−; TdT+) of the nasopharynx extending to the deep
 and superficial structures of the right hemiface, to the skull base with an intracranial component and a small but detectable
 bone marrow involvement, who was started on chemotherapy with a complete response. To the best of our knowledge, this is the
 first case of a primary nasopharynx B-LBL in an adult patient with such aggressive regional spread to be reported in the literature.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0206-2Authors
		Rodrigo Lopes da Silva, Serviço de Hematologia, Hospital Santo António dos Capuchos, Alameda Santo António dos Capuchos, 1169-050 Lisbon, PortugalTeresa F...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3897856</comments>
            <pubDate>Sat, 21 Aug 2010 16:45:39 +0100</pubDate>
            <guid isPermaLink="false">3897856</guid>        </item>
        <item>
            <title>Sarcomatoid (Spindle Cell) Carcinoma of the Head and Neck Mucosal Region: A Clinicopathologic Review of 103 Cases from a Tertiary Referral Cancer Centre</title>
            <link>http://www.medworm.com/index.php?rid=3897857&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh247594075681334%2F</link>
            <description>This study evaluates their clinicopathologic characteristics in head and neck mucosal sites and the problems in distinguishing
 them from other spindle cell tumors. A total of 103 cases with a confirmed diagnosis of sarcomatoid carcinoma accessioned
 in the pathology department of a tertiary referral cancer centre over a period of 7&amp;nbsp;years (2004–2010) were studied. An algorithm
 used for their diagnosis is presented. Ages of the patients were 22–90&amp;nbsp;years (median 53&amp;nbsp;years), and male:female ratio was
 3.7:1. Site distribution was oral cavity (n = 65, 63.1%), larynx (18, 17.5%), oropharynx/hypopharynx (12, 10.7%), maxilla (6, 5.8%) and metastatic nodes (2, 1.9%). A
 large number of patients (95%) presented with a mass lesion of less than 1&amp;nbsp;year duration. Histopathologic...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3897857</comments>
            <pubDate>Sat, 21 Aug 2010 16:45:38 +0100</pubDate>
            <guid isPermaLink="false">3897857</guid>        </item>
        <item>
            <title>Bazex Syndrome (Acrokeratosis Paraneoplastica) Diagnosed in a Patient with Oral Persistent Ulcerations</title>
            <link>http://www.medworm.com/index.php?rid=3883567&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa45q57xr84v88klw%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Paraneoplastic syndromes associated with head and neck cancer are rare and have been reported under dermatological, endocrine,
 hematological, neurological and rheumatological disorders. Bazex syndrome is an intriguing paraneoplasia that can be associated
 with head and neck squamous cell carcinomas. A range of symmetrical dermatological manifestations, with a clear predilection
 to extremities, that encompasses erythematous squamous plaques, skin scaling and nail dystrophy can provide a psoriasiform
 pattern in Bazex syndrome. In addition to these tricky clinical features, the rarity of the disease and the lack of understanding
 on Bazex syndrome generally make such cases to be mismanaged as psoriasis or lichen planus, causing an important delay in
 the diagnosis of th...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3883567</comments>
            <pubDate>Wed, 18 Aug 2010 17:44:33 +0100</pubDate>
            <guid isPermaLink="false">3883567</guid>        </item>
        <item>
            <title>Squamous Odontogenic Tumor</title>
            <link>http://www.medworm.com/index.php?rid=3866323&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq87811q182324130%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 24&amp;nbsp;year male presented with a radiolucent lesion associated with the right maxillary canine. Histologic examination of the
 biopsy material resulted in a diagnosis of squamous odontogenic tumor a rare, benign epithelial odontogenic neoplasm. The
 clinical, radiographic and morphologic features of the squamous odontogenic tumor are discussed.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0198-yAuthors
		Bradley E. Jones, Joint POW-MIA Accounting Command, Hickam AFB, HI USAAaron P. Sarathy, Oral and Maxillofacial Surgery, Naval Hospital, Beaufort, SC USAM. Belinda Ramos, Laboratory Department, Naval Hospital, Jacksonville, FL USARobert D. Foss, Department of Oral and Maxillofacial Pathology, Armed Forces Institute of Pathology, Room 3055, 6825 16th Street...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3866323</comments>
            <pubDate>Mon, 09 Aug 2010 19:40:39 +0100</pubDate>
            <guid isPermaLink="false">3866323</guid>        </item>
        <item>
            <title>Collision Tumor of Primary Laryngeal Mucosal Melanoma and Invasive Squamous Cell Carcinoma with IL-17A and CD70 Gene Over-Expression</title>
            <link>http://www.medworm.com/index.php?rid=3866324&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg8n3602838j52851%2F</link>
            <description>We report a 53-year-old
 male patient who was diagnosed with a collision tumor of laryngeal melanoma and invasive SCC. Multiple Th17 pathway related
 genes including CTLA-4, IL-17A-F, PLZF, FoxP3, RorγT, CD27, and CD70 were analyzed by reverse transcriptase-polymerase chain
 reaction (Rt–PCR) in this case. Both IL-17A and CD70 genes were detected in this case of collision tumor. The results may
 define useful biomarkers for early diagnosis of mucosal melanoma and open an immunotherapeutic field for clinical management
 with the potential benefit from the immunomodulators that enhance both genes.
 
 
	Content Type Journal ArticleDOI 10.1007/s12105-010-0200-8Authors
		Sasis Sirikanjanapong, Department of Pathology, New York University School of Medicine, 550 First Avenue, TCH-461, New Yor...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3866324</comments>
            <pubDate>Mon, 09 Aug 2010 19:40:38 +0100</pubDate>
            <guid isPermaLink="false">3866324</guid>        </item>
        <item>
            <title>Epstein-Barr Virus-Associated Smooth Muscle Tumor of the Larynx: Report of a Rare Case Mimicking Leiomyosarcoma</title>
            <link>http://www.medworm.com/index.php?rid=3832623&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx817l641255k7vq8%2F</link>
            <description>We present a patient (male 54&amp;nbsp;years) with a history of renal transplant who 14&amp;nbsp;years post transplantation developed a symptomatic
 (stridor) laryngeal Epstein Barr virus (EBV)—associated smooth muscle tumor (EBV-SMT) in the absence of concomitant disease
 elsewhere. Nine years post transplantation the patient developed a subcutaneous EBV-SMT tumor located on the calf. The laryngeal
 tumor displayed low-grade nuclear atypia and was infiltrating into the surrounding soft tissue, focally ulcerating through
 the overlying epithelium. Histologic features included: neoplastic cells with myoid differentiation, a component of primitive
 appearing small mesenchymal cells with hyperchromatic nuclei, mitotic activity, intralesional small to medium sized blood
 vessels and T-lymphocytes. B...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3832623</comments>
            <pubDate>Fri, 06 Aug 2010 07:14:35 +0100</pubDate>
            <guid isPermaLink="false">3832623</guid>        </item>
        <item>
            <title>Clinical–Pathological Conference: Case 4</title>
            <link>http://www.medworm.com/index.php?rid=3811041&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft62l5884u8728224%2F</link>
            <description>Content Type Journal ArticleCategory 64TH ANNUAL MEETING OF THE AMERICAN ACADEMY OF ORAL AND MAXILLOFACIAL PATHOLOGYDOI 10.1007/s12105-010-0195-1Authors
		Kristin K. McNamara, The Ohio State University 305 West 12th Ave. Columbus OH 43210 USAMikelle L. Kernig, USAF, Wright Patterson AFB Dayton OH USAKelly S. Kreuter, The Ohio State University 305 West 12th Ave. Columbus OH 43210 USAJohn R. Kalmar, The Ohio State University 305 West 12th Ave. Columbus OH 43210 USACarl M. Allen, The Ohio State University 305 West 12th Ave. Columbus OH 43210 USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3811041</comments>
            <pubDate>Fri, 30 Jul 2010 17:25:16 +0100</pubDate>
            <guid isPermaLink="false">3811041</guid>        </item>
        <item>
            <title>Clinical–Pathological Conference: Case 2</title>
            <link>http://www.medworm.com/index.php?rid=3811040&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb1178x323n736n08%2F</link>
            <description>Content Type Journal ArticleCategory 64TH ANNUAL MEETING OF THE AMERICAN ACADEMY OF ORAL AND MAXILLOFACIAL PATHOLOGYDOI 10.1007/s12105-010-0192-4Authors
		Nasser Said-Al-Naief, University of the Pacific OMFP Laboratory and Clinical Oral Pathology/Oral Medicine, Room 412, Department of Pathology and Medicine 2155 Webster Street San Francisco CA 94115-2333 USAMolly S. Rosebush, University of Tennessee College of Dentistry Department of Biologic and Diagnostic Sciences Memphis TN USADenis Lynch, Marquette University School of Dentistry, Academic Affairs Milwaukee WI USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3811040</comments>
            <pubDate>Fri, 30 Jul 2010 17:25:16 +0100</pubDate>
            <guid isPermaLink="false">3811040</guid>        </item>
        <item>
            <title>Clinical–Pathological Conference: Case 6</title>
            <link>http://www.medworm.com/index.php?rid=3811043&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Far3332u1m32p3774%2F</link>
            <description>Content Type Journal ArticleCategory 64TH ANNUAL MEETING OF THE AMERICAN ACADEMY OF ORAL AND MAXILLOFACIAL PATHOLOGYDOI 10.1007/s12105-010-0196-0Authors
		Joseph C. Whitt, University of Missouri Kansas City Oral and Maxillofacial Pathology, School of Dentistry Kansas City MO USABrian S. Shumway, University of Louisville School of Dentistry Department of Surgical and Hospital Dentistry Louisville KY USAElliot A. Magidson, Wichita Clinic Pathology Department Wichita KS USARoy E. Cole, Oral and Maxillofacial Surgery Private Practice Wichita KS USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3811043</comments>
            <pubDate>Fri, 30 Jul 2010 17:25:15 +0100</pubDate>
            <guid isPermaLink="false">3811043</guid>        </item>
        <item>
            <title>Methotrexate-Related Epstein-Barr Virus (EBV)-Associated Lymphoproliferative Disorder—So-Called “Hodgkin-Like Lesion”—of the Oral Cavity in a Patient with Rheumatoid Arthritis</title>
            <link>http://www.medworm.com/index.php?rid=3811042&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjm3266147243l714%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Patients affected by autoimmune diseases (rheumatoid arthritis, psoriasis, dermatomyositis) who are treated with methotrexate
 (MTX) sometimes develop lymphoproliferative disorders (LPDs). In approximately 40% of reported cases, the affected sites have
 been extranodal, and have included the gastrointestinal tract, skin, lung, kidney, and soft tissues. However, MTX-associated
 LPD (MTX-LPD) is extremely rare in the oral cavity. Here we report a 69-year-old Japanese woman with rheumatoid arthritis
 (RA) who developed MTX-LPD resembling Hodgkin’s disease—so-called “Hodgkin-like lesion”—in the left upper jaw. Histopathologically,
 large atypical lymphoid cells including Hodgkin or Reed-Sternberg-like cells were found to have infiltrated into granulation
 tissue i...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3811042</comments>
            <pubDate>Fri, 30 Jul 2010 17:25:15 +0100</pubDate>
            <guid isPermaLink="false">3811042</guid>        </item>
        <item>
            <title>Clinical–Pathological Conference: Case 3</title>
            <link>http://www.medworm.com/index.php?rid=3811044&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr72387n5554t6g52%2F</link>
            <description>Content Type Journal ArticleCategory 64TH ANNUAL MEETING OF THE AMERICAN ACADEMY OF ORAL AND MAXILLOFACIAL PATHOLOGYDOI 10.1007/s12105-010-0199-xAuthors
		James M. Hall, Tufts University School of Dental Medicine Department of Oral and Maxillofacial Pathology 1 Kneeland St. Boston MA 02111 USAKevin R. Torske, Naval Postgraduate Dental School Department of Oral and Maxillofacial Pathology Bethesda MD USAMichael A. Kahn, Tufts University School of Dental Medicine Department of Oral and Maxillofacial Pathology 1 Kneeland St. Boston MA 02111 USAAdele A. Moreland, Lahey Clinic Medical Center Department of Dermatology Burlington MA USASamuel L. Moschella, Lahey Clinic Medical Center Department of Dermatology Burlington MA USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISS...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3811044</comments>
            <pubDate>Fri, 30 Jul 2010 17:25:14 +0100</pubDate>
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        <item>
            <title>Clinical–Pathological Conference: Case 5</title>
            <link>http://www.medworm.com/index.php?rid=3811045&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F944j1p1754210n12%2F</link>
            <description>Content Type Journal ArticleCategory 64TH ANNUAL MEETING OF THE AMERICAN ACADEMY OF ORAL AND MAXILLOFACIAL PATHOLOGYDOI 10.1007/s12105-010-0194-2Authors
		Craig B. Fowler, 59 Dental Training Squadron/SGDTM Oral and Maxillofacial Pathology 2200 Bergquist Drive Suite 1, Lackland AFB San Antonio TX 78236-5300 USANisha J. D’Silva, University of Michigan School of Dentistry Department of Periodontics and Oral Medicine 1011 North University Avenue, Room G018 Ann Arbor MI 48109-1078 USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3811045</comments>
            <pubDate>Fri, 30 Jul 2010 17:25:13 +0100</pubDate>
            <guid isPermaLink="false">3811045</guid>        </item>
        <item>
            <title>Calcifying Cystic Odontogenic Tumor</title>
            <link>http://www.medworm.com/index.php?rid=3792624&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc0r6314071672164%2F</link>
            <description>Content Type Journal ArticleCategory Sine qua none Radiology-PathologyDOI 10.1007/s12105-010-0197-zAuthors
		Ximena Zornosa, Clayton State University Department of Dental Hygiene, College of Health 2000 Clayton State Boulevard Morrow GA 30260 USASusan Müller, Emory University School of Medicine Department of Pathology and Laboratory Medicine, Department of Otolaryngology Head and Neck Surgery, Winship Cancer Institute 1365 Clifton Rd, NE, Room A2134 Atlanta GA 30322 USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3792624</comments>
            <pubDate>Sat, 24 Jul 2010 13:52:12 +0100</pubDate>
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        <item>
            <title>Clinical–Pathological Conference: Case 1</title>
            <link>http://www.medworm.com/index.php?rid=3792623&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flm53k4106q8q7p8w%2F</link>
            <description>Content Type Journal ArticleCategory 64TH ANNUAL MEETING OF THE AMERICAN ACADEMY OF ORAL AND MAXILLOFACIAL PATHOLOGYDOI 10.1007/s12105-010-0193-3Authors
		Ilana Kaplan, Tel-Aviv Sourasky Medical Center Institute of Pathology 6 Weitzman St Tel Aviv IsraelSonal S. Shah, New York University Department of Oral and Maxillofacial Pathology, Radiology, and Medicine, College of Dentistry New York NY USAZoe Nicolaou-Ioannou, Private Oral and Maxillofacial Surgery Limassol CyprusDan M. Fliss, Tel-Aviv Sourasky Medical Center Department of Otolaryngology, Head and Neck Surgery Tel Aviv Israel
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3792623</comments>
            <pubDate>Sat, 24 Jul 2010 13:52:12 +0100</pubDate>
            <guid isPermaLink="false">3792623</guid>        </item>
        <item>
            <title>Central Mucoepidermoid Carcinoma, A Case Report with Molecular Analysis of the TORC1/MAML2 Gene Fusion</title>
            <link>http://www.medworm.com/index.php?rid=3756158&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv811528100736136%2F</link>
            <description>We report an example of intraosseous mucoepidermoid carcinoma with positive TORC1/MAML2 gene
 fusion transcript and discuss the clinical implications.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s12105-010-0191-5Authors
		Haseeb Ahmed Khan, Shaukat Khanum Memorial Cancer Hospital &amp; Research Centre Department of Pathology Johar Town, Lahore PakistanAsif Loya, Shaukat Khanum Memorial Cancer Hospital &amp; Research Centre Department of Pathology Johar Town, Lahore PakistanRafay Azhar, Shaukat Khanum Memorial Cancer Hospital &amp; Research Centre Department of Pathology Johar Town, Lahore PakistanNasir Ud Din, Aga Khan University Hospital Department of Pathology Karachi PakistanDiana Bell, The University of Texas M.D. Anderson Cancer Center Department of Pathology Houston TX USA
	...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3756158</comments>
            <pubDate>Tue, 13 Jul 2010 15:39:13 +0100</pubDate>
            <guid isPermaLink="false">3756158</guid>        </item>
        <item>
            <title>Molecular and Clinicopathological Findings in a Tonsillar Synovial Sarcoma. A Case Study and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=3756159&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl323x7p8h2400j86%2F</link>
            <description>We describe the case of
 a 31-year-old male who presented with biphasic SS with poorly differentiated areas (clinical stage IIA) in a palatine tonsil,
 an extremely rare site of SS. Molecular analyses revealed typical t(X;18) translocation of the SYT gene and a SYT/SSX1 fusion
 type. The tumor was surgically resected with free margins. Adjuvant radiotherapy or chemotherapy was not considered indicated.
 To date, the patient has remained free of tumor for 4&amp;nbsp;years after surgery. Literature review reveals that primary tonsillar
 HNSS has previously been documented only in three patients. In all of these patients the tumor was histologically biphasic;
 however only one published case and the case presented here showed areas of poor differentiation. We discuss the relevance
 of the present...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3756159</comments>
            <pubDate>Tue, 13 Jul 2010 15:39:04 +0100</pubDate>
            <guid isPermaLink="false">3756159</guid>        </item>
        <item>
            <title>A Case of Odontogenic Myxoma with Unusual Histological Features Mimicking a Fibro-Osseous Process</title>
            <link>http://www.medworm.com/index.php?rid=3735516&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff2p305vkjw582512%2F</link>
            <description>This report describes a case of odontogenic
 myxoma producing diffusely dispersed calcified products in a pattern reminiscent of a fibro-osseous lesion of the jaw. Differential
 diagnoses for myxoid lesions of the jaws also are discussed. This paper highlights how an odontogenic myxoma can produce a
 large amount of calcified products to mimic a fibro-osseous process.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s12105-010-0189-zAuthors
		Yi-Ling Lin, University of California at Los Angeles, School of Dentistry Department of Diagnostic and Surgical Sciences 10833 Le Conte Ave. Los Angeles CA 90095 USAJohn R. Basile, University of Maryland Dental School Department of Oncology and Diagnostic Sciences 650 W. Baltimore St., 7-North Baltimore MD 21201 USA
	

	
		Journal Hea...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3735516</comments>
            <pubDate>Tue, 06 Jul 2010 17:07:26 +0100</pubDate>
            <guid isPermaLink="false">3735516</guid>        </item>
        <item>
            <title>Large Cell Neuroendocrine Carcinoma of the Larynx: Definition of an Entity</title>
            <link>http://www.medworm.com/index.php?rid=3716521&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdx047246481ml332%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Laryngeal atypical carcinoids (AC/moderately-differentiated neuroendocrine carcinoma) are associated with moderately aggressive
 clinical behavior; however, a subset of tumors classified as AC have much greater aggressive potential. These tumors fulfill
 the proposed diagnostic criteria for pulmonary large cell neuroendocrine carcinoma, albeit in the larynx. In the current WHO
 classification, laryngeal large cell neuroendocrine carcinomas (LCNEC) are classified as variants of AC, whereas pulmonary LCNEC are classified as poorly-differentiated neuroendocrine carcinomas. Reported outcomes for pulmonary
 tumors support the separate classification of LCNEC. Five and ten year survival rates for pulmonary AC are 61–73, and 35–59%,
 respectively, while the 5-year survival...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3716521</comments>
            <pubDate>Tue, 29 Jun 2010 16:34:52 +0100</pubDate>
            <guid isPermaLink="false">3716521</guid>        </item>
        <item>
            <title>Sialolipoma in Minor Salivary Gland: Case Report and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=3689256&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F97624750v347762j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Sialolipoma is a rare benign neoplasm characterized by a well-circumscribed mass composed of neoplastic mature adipose tissue
 and non-neoplastic salivary gland elements. A 72-year-old woman presented with a painless swelling located in the hard palate,
 which had been identified 15&amp;nbsp;days earlier. Microscopically, the tumor was well-circumscribed consisting of lobular proliferation
 of the lipomatous tissue with thin fibrous tissue septa containing clustered salivary gland elements. Both the glandular and
 adipose components were found in almost equal proportion. No atypia in the adipose tissue was observed. The definitive diagnosis
 was sialolipoma. The patient showed no signs of recurrence 8&amp;nbsp;months after surgical excision. Including the present case, 35
 case...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3689256</comments>
            <pubDate>Sun, 20 Jun 2010 23:09:33 +0100</pubDate>
            <guid isPermaLink="false">3689256</guid>        </item>
        <item>
            <title>Intraosseous Ameloblastoma with a Prominent Extraosseous Component: Pitfalls in Diagnosis</title>
            <link>http://www.medworm.com/index.php?rid=3669154&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffg11358737536176%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;For many years, gingival tumors of what appear to be peripherally located intraosseous ameloblastoma (IA) arising from the
 alveolar bone surface have often been confused with peripheral ameloblastoma (PA) causing resorption of the underlying bone.
 We analyzed a series of five cases of ameloblastoma that demonstrated a combined PA and IA architecture. The tumor commonly
 involved the anterior-premolar area, mostly in the maxilla and mainly in middle-aged men. The clinical presentation was an
 exophytic gingival mass inferior to which was a small bone defect. The predominant extraosseous component showed a papillary
 gross surface, reflecting the histologic proof of fusion between the submucosal tumor and the surface epithelium. In addition
 to the PA-like growth patter...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3669154</comments>
            <pubDate>Mon, 14 Jun 2010 13:52:45 +0100</pubDate>
            <guid isPermaLink="false">3669154</guid>        </item>
        <item>
            <title>Intranasal Eosinophilic Angiocentric Fibrosis: A Case Report and Review</title>
            <link>http://www.medworm.com/index.php?rid=3654469&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7789851786263251%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Eosinophilc angiocentric fibrosis is a rare fibrosing vasculitis of unknown etiology that is progressive and potentially disfiguring.
 It has a predilection for the upper airways presenting most commonly as an obstructing mass lesion that is diagnosed histologically.
 Thus far, it has been nonfatal in the more than 40 reported cases; however, subglottic and ocular involvement has resulted
 in significant morbidity in several patients. Treatment has been challenging with persistent disease in most cases. The current
 case is a prototypical presentation with a limited nasal septal lesion providing the opportunity to discuss clinically relevant
 issues and increase awareness.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s12105-010-0185-3Authors
		Jumin ...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3654469</comments>
            <pubDate>Wed, 09 Jun 2010 09:24:58 +0100</pubDate>
            <guid isPermaLink="false">3654469</guid>        </item>
        <item>
            <title>Compound Odontoma</title>
            <link>http://www.medworm.com/index.php?rid=3654470&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn27109u27852n376%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A case of compound odontomas of the anterior maxilla is discussed. Multiple tooth like structures were discovered upon surgical
 excision.
 
 
	Content Type Journal ArticleCategory Sine qua none Radiology-PathologyDOI 10.1007/s12105-010-0186-2Authors
		Brenda L. Nelson, Naval Medical Center San Diego Department of Anatomic Pathology 34800 Bob Wilson Drive San Diego CA 92134-5000 USALester D. R. Thompson, Naval Medical Center San Diego Department of Anatomic Pathology 34800 Bob Wilson Drive San Diego CA 92134-5000 USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3654470</comments>
            <pubDate>Wed, 09 Jun 2010 09:24:57 +0100</pubDate>
            <guid isPermaLink="false">3654470</guid>        </item>
        <item>
            <title>Primary Diffuse Large B-Cell Lymphoma of the Oral Cavity: Germinal Center Classification</title>
            <link>http://www.medworm.com/index.php?rid=3654471&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwm571078m1830873%2F</link>
            <description>In conclusion, our analysis shows that primary oral DLBCL
 predominantly belongs to the non-GCB subgroup, which tends to exhibit a poorer prognosis. These findings could allow pathologists
 to provide a more accurate insight into the potential aggressive behavior and poorer prognosis of these lymphomas.
 
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s12105-010-0184-4Authors
		Indraneel Bhattacharyya, University of Florida College of Dentistry Department of Oral and Maxillofacial Diagnostic Sciences PO Box 100414 Gainesville FL 32610 USAHardeep K. Chehal, Creighton University School of Dentistry Department of General Dentistry Omaha NE USADonald M. Cohen, University of Florida College of Dentistry Department of Oral and Maxillofacial Diagnostic Sciences PO Box 100414 Ga...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3654471</comments>
            <pubDate>Wed, 09 Jun 2010 09:24:56 +0100</pubDate>
            <guid isPermaLink="false">3654471</guid>        </item>
        <item>
            <title>Nerve Sheath Myxoma (Neurothekeoma) of the Gingiva, A Case Report and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=3611382&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp18j5h3k4706071n%2F</link>
            <description>In this report, we describe the first gingival case
 of oral neurothekeoma with histopathologic and immunohistochemical characteristics. The patient, a 32&amp;nbsp;year old female presented
 with a slowly growing gingival mass diagnosed clinically as an epulis. The lesion was surgically excised. Histopathologically,
 the lesion presented as a submucosal multinodular mass composed of spindle and stellate-shaped cells with a myxoid background.
 Immunohistochemically, the tumor cells were sporadically positive for S-100 and NSE and negative for GFAP, EMA, SMA, CD68
 and HMB45. The immunoprofile of this lesion confirmed a Schwann cell origin. The lesion was followed up for 10&amp;nbsp;months with
 no reports of recurrence.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s12105-010-018...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3611382</comments>
            <pubDate>Tue, 25 May 2010 16:52:09 +0100</pubDate>
            <guid isPermaLink="false">3611382</guid>        </item>
        <item>
            <title>Nasopharyngeal Angiofibroma of the Nasal Cavity</title>
            <link>http://www.medworm.com/index.php?rid=3565519&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp23r14176664q336%2F</link>
            <description>Content Type Journal ArticleCategory Sine qua none Radiology-PathologyDOI 10.1007/s12105-010-0181-7Authors
		S. Marc Stokes, Naval Postgraduate Dental School, NMMPT&amp;E Department of Oral &amp; Maxillofacial Pathology 8901 Wisconsin Ave. Bethesda MD 20889-5611 USAJames T. Castle, Naval Postgraduate Dental School, NMMPT&amp;E Department of Oral &amp; Maxillofacial Pathology 8901 Wisconsin Ave. Bethesda MD 20889-5611 USA
	

	
		Journal Head and Neck PathologyOnline ISSN 1936-0568Print ISSN 1936-055X (Source: Head and Neck Pathology)</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3565519</comments>
            <pubDate>Thu, 13 May 2010 08:59:06 +0100</pubDate>
            <guid isPermaLink="false">3565519</guid>        </item>
        <item>
            <title>Primary Lingual Tuberculosis in Immunocompetent Patient: a Case Report</title>
            <link>http://www.medworm.com/index.php?rid=3565520&amp;cid=s_35965_32_f&amp;fid=35965&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn05u813850w31215%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Oral manifestations of tuberculosis are quite rare with an incidence rate of 1.4%. The tongue is the most common site of oral
 tuberculosis having varied presentations. Lingual tuberculosis is a diagnostic dilemma because of its rarity, particularly
 in immunocompetent patients. We are reporting a rare case of primary tuberculosis of the tongue in a 38&amp;nbsp;year old male diagnosed
 on fine needle aspiration cytology.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s12105-010-0180-8Authors
		Sanjay Kumar, 4/9J, Medical Enclave, PGIMS Rohtak 124001 Haryana IndiaRajeev Sen, PGIMS Department of Pathology Rohtak 124001 Haryana IndiaAnju Rawal, PGIMS Department of Pathology Rohtak 124001 Haryana IndiaRanbir Singh Dahiya, PGIMS Department of Surgery Rohtak 124...</description>
            <author>Head and Neck Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3565520</comments>
            <pubDate>Thu, 13 May 2010 08:59:05 +0100</pubDate>
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