Divergent Myoid, Neuroendocrine, and Perineural Differentiation in a Nasal Tumor of a Patient With Carney Complex
A 39-year-old woman with Carney complex presented with a stroke of undetermined etiology. Computed tomography showed bilateral thalamic infarctions and also an unsuspected multicompartmental cystic neoplasm that had eroded the anterior clivus and extended forward into the nasopharynx. Histologically...
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description | A 39-year-old woman with Carney complex presented with a stroke of undetermined etiology. Computed tomography showed bilateral thalamic infarctions and also an unsuspected multicompartmental cystic neoplasm that had eroded the anterior clivus and extended forward into the nasopharynx. Histologically, the mass appeared benign and was composed of spindle cells and multiple foci of striated muscle. Immunohistochemically, the spindle cells were strongly reactive for S-100 protein and to a lesser extent for CD57, collagen IV, neuron-specific enolase, smooth muscle actin, epithelial membrane antigen, and glut-1. The striated muscle cells were positive for desmin and myogenin. The MIB-1 labeling index was 0.5%. Ultrastructural examination was necessary to reveal the full extent of divergent differentiation. Ultrastructurally, the spindle cells showed divergent differentiation along several cell lines, including smooth muscle, neuroendocrine, hybrid smooth muscle-neuroendocrine, perineural-like cells, and striated muscle. The occurrence of this unique lesion in a patient with the Carney complex raises the possibility that it may be a rare component of the syndrome. |
doi_str_mv | 10.1097/PAS.0b013e31813c0e11 |
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Computed tomography showed bilateral thalamic infarctions and also an unsuspected multicompartmental cystic neoplasm that had eroded the anterior clivus and extended forward into the nasopharynx. Histologically, the mass appeared benign and was composed of spindle cells and multiple foci of striated muscle. Immunohistochemically, the spindle cells were strongly reactive for S-100 protein and to a lesser extent for CD57, collagen IV, neuron-specific enolase, smooth muscle actin, epithelial membrane antigen, and glut-1. The striated muscle cells were positive for desmin and myogenin. The MIB-1 labeling index was 0.5%. Ultrastructural examination was necessary to reveal the full extent of divergent differentiation. Ultrastructurally, the spindle cells showed divergent differentiation along several cell lines, including smooth muscle, neuroendocrine, hybrid smooth muscle-neuroendocrine, perineural-like cells, and striated muscle. The occurrence of this unique lesion in a patient with the Carney complex raises the possibility that it may be a rare component of the syndrome.</description><identifier>ISSN: 0147-5185</identifier><identifier>EISSN: 1532-0979</identifier><identifier>DOI: 10.1097/PAS.0b013e31813c0e11</identifier><identifier>PMID: 18162785</identifier><identifier>CODEN: AJSPDX</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Female ; Humans ; Immunohistochemistry ; Investigative techniques, diagnostic techniques (general aspects) ; Medical sciences ; Microscopy, Electron, Transmission ; Middle Aged ; Neoplasms, Muscle Tissue - metabolism ; Neoplasms, Muscle Tissue - ultrastructure ; Neoplastic Syndromes, Hereditary - complications ; Neoplastic Syndromes, Hereditary - metabolism ; Neoplastic Syndromes, Hereditary - pathology ; Nose Neoplasms - metabolism ; Nose Neoplasms - ultrastructure ; Pathology. 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Computed tomography showed bilateral thalamic infarctions and also an unsuspected multicompartmental cystic neoplasm that had eroded the anterior clivus and extended forward into the nasopharynx. Histologically, the mass appeared benign and was composed of spindle cells and multiple foci of striated muscle. Immunohistochemically, the spindle cells were strongly reactive for S-100 protein and to a lesser extent for CD57, collagen IV, neuron-specific enolase, smooth muscle actin, epithelial membrane antigen, and glut-1. The striated muscle cells were positive for desmin and myogenin. The MIB-1 labeling index was 0.5%. Ultrastructural examination was necessary to reveal the full extent of divergent differentiation. Ultrastructurally, the spindle cells showed divergent differentiation along several cell lines, including smooth muscle, neuroendocrine, hybrid smooth muscle-neuroendocrine, perineural-like cells, and striated muscle. The occurrence of this unique lesion in a patient with the Carney complex raises the possibility that it may be a rare component of the syndrome.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Transmission</subject><subject>Middle Aged</subject><subject>Neoplasms, Muscle Tissue - metabolism</subject><subject>Neoplasms, Muscle Tissue - ultrastructure</subject><subject>Neoplastic Syndromes, Hereditary - complications</subject><subject>Neoplastic Syndromes, Hereditary - metabolism</subject><subject>Neoplastic Syndromes, Hereditary - pathology</subject><subject>Nose Neoplasms - metabolism</subject><subject>Nose Neoplasms - ultrastructure</subject><subject>Pathology. Cytology. 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Miscellaneous investigative techniques</subject><subject>Perineum - pathology</subject><subject>Stroke - complications</subject><issn>0147-5185</issn><issn>1532-0979</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkEtLxDAUhYMoOj7-gUg2urKaNJNpupTxCT4GVFyW2_RGI20yk7Ti_HszOCC4yiXnO9_iEHLI2RlnZXE-u3g-YzXjAgVXXGiGnG-QEZciz1JebpIR4-Mik1zJHbIb4ydjPFc83yY7qTDJCyVHZHFpvzC8o-vpw9Lb5pQ-4hA8usbrYB2eUnANneHqHgK09NIagyHxFnrrHbWOAn2EmKKXofOBepM-ZilcOd9s_0GnEBwu6dR38xa_98mWgTbiwfrdI6_XVy_T2-z-6eZuenGfaSFkn5mJLHTe5ChNPWFG5WWdK8XHAmoDCEqOawWoG8YQDWgzSYCpsdRYAgdsxB45-fXOg18MGPuqs1Fj24JDP8SqYLxgTIkEjn9BHXyMAU01D7aDsKw4q1ZTV2nq6v_UqXa09g91h81fab1tAo7XAEQNrQngtI1_XFkqJZP0B3z5ilo</recordid><startdate>2008</startdate><enddate>2008</enddate><creator>DAO, Linda N</creator><creator>SCHEITHAUER, Bernd W</creator><creator>ERLANDSON, Robert A</creator><creator>YOUNG, William F</creator><creator>AIDAN CARNEY, J</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2008</creationdate><title>Divergent Myoid, Neuroendocrine, and Perineural Differentiation in a Nasal Tumor of a Patient With Carney Complex</title><author>DAO, Linda N ; SCHEITHAUER, Bernd W ; ERLANDSON, Robert A ; YOUNG, William F ; AIDAN CARNEY, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c335t-f657c2d2e5fb60f829b288143abfaea854b8aecd00eefacf629bfbe9ce9a1aed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Medical sciences</topic><topic>Microscopy, Electron, Transmission</topic><topic>Middle Aged</topic><topic>Neoplasms, Muscle Tissue - metabolism</topic><topic>Neoplasms, Muscle Tissue - ultrastructure</topic><topic>Neoplastic Syndromes, Hereditary - complications</topic><topic>Neoplastic Syndromes, Hereditary - metabolism</topic><topic>Neoplastic Syndromes, Hereditary - pathology</topic><topic>Nose Neoplasms - metabolism</topic><topic>Nose Neoplasms - ultrastructure</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Perineum - pathology</topic><topic>Stroke - complications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DAO, Linda N</creatorcontrib><creatorcontrib>SCHEITHAUER, Bernd W</creatorcontrib><creatorcontrib>ERLANDSON, Robert A</creatorcontrib><creatorcontrib>YOUNG, William F</creatorcontrib><creatorcontrib>AIDAN CARNEY, J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of surgical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DAO, Linda N</au><au>SCHEITHAUER, Bernd W</au><au>ERLANDSON, Robert A</au><au>YOUNG, William F</au><au>AIDAN CARNEY, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Divergent Myoid, Neuroendocrine, and Perineural Differentiation in a Nasal Tumor of a Patient With Carney Complex</atitle><jtitle>The American journal of surgical pathology</jtitle><addtitle>Am J Surg Pathol</addtitle><date>2008</date><risdate>2008</risdate><volume>32</volume><issue>1</issue><spage>167</spage><epage>171</epage><pages>167-171</pages><issn>0147-5185</issn><eissn>1532-0979</eissn><coden>AJSPDX</coden><abstract>A 39-year-old woman with Carney complex presented with a stroke of undetermined etiology. Computed tomography showed bilateral thalamic infarctions and also an unsuspected multicompartmental cystic neoplasm that had eroded the anterior clivus and extended forward into the nasopharynx. Histologically, the mass appeared benign and was composed of spindle cells and multiple foci of striated muscle. Immunohistochemically, the spindle cells were strongly reactive for S-100 protein and to a lesser extent for CD57, collagen IV, neuron-specific enolase, smooth muscle actin, epithelial membrane antigen, and glut-1. The striated muscle cells were positive for desmin and myogenin. The MIB-1 labeling index was 0.5%. Ultrastructural examination was necessary to reveal the full extent of divergent differentiation. Ultrastructurally, the spindle cells showed divergent differentiation along several cell lines, including smooth muscle, neuroendocrine, hybrid smooth muscle-neuroendocrine, perineural-like cells, and striated muscle. The occurrence of this unique lesion in a patient with the Carney complex raises the possibility that it may be a rare component of the syndrome.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>18162785</pmid><doi>10.1097/PAS.0b013e31813c0e11</doi><tpages>5</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Female Humans Immunohistochemistry Investigative techniques, diagnostic techniques (general aspects) Medical sciences Microscopy, Electron, Transmission Middle Aged Neoplasms, Muscle Tissue - metabolism Neoplasms, Muscle Tissue - ultrastructure Neoplastic Syndromes, Hereditary - complications Neoplastic Syndromes, Hereditary - metabolism Neoplastic Syndromes, Hereditary - pathology Nose Neoplasms - metabolism Nose Neoplasms - ultrastructure Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Perineum - pathology Stroke - complications |
title | Divergent Myoid, Neuroendocrine, and Perineural Differentiation in a Nasal Tumor of a Patient With Carney Complex |
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