Pilomatrical carcinosarcoma of the temple: A case report
Pilomatrical carcinosarcoma is a very rare entity, with only six cases reported until now. This report describes the case of a 100‐year‐old woman with a mass on the left temple that had existed for several decades but had recently grown in size. Histology showed an asymmetric lesion composed of basa...
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Veröffentlicht in: | Journal of cutaneous pathology 2019-04, Vol.46 (4), p.267-270 |
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description | Pilomatrical carcinosarcoma is a very rare entity, with only six cases reported until now. This report describes the case of a 100‐year‐old woman with a mass on the left temple that had existed for several decades but had recently grown in size. Histology showed an asymmetric lesion composed of basaloid cells, spindle cells, and “shadow” or “ghost” cells. Cells had atypical hyperchromatic nuclei with prominent nucleoli, high mitotic activity, and atypical mitosis. In the central area, an epidermal cyst‐like structure was seen. The diagnosis of pilomatrical carcinosarcoma was rendered. This case appeared to have arisen from malignant transformation of a pilomatricoma because of the long clinical history and existence of a benign epidermal cyst‐like structure. In addition, the observation that the basaloid cells and spindle cells showed a gradual transition from one to the other and that both types were positive for β‐catenin would seem to support a common clonal origin for the carcinomatous and sarcomatous components. |
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This report describes the case of a 100‐year‐old woman with a mass on the left temple that had existed for several decades but had recently grown in size. Histology showed an asymmetric lesion composed of basaloid cells, spindle cells, and “shadow” or “ghost” cells. Cells had atypical hyperchromatic nuclei with prominent nucleoli, high mitotic activity, and atypical mitosis. In the central area, an epidermal cyst‐like structure was seen. The diagnosis of pilomatrical carcinosarcoma was rendered. This case appeared to have arisen from malignant transformation of a pilomatricoma because of the long clinical history and existence of a benign epidermal cyst‐like structure. In addition, the observation that the basaloid cells and spindle cells showed a gradual transition from one to the other and that both types were positive for β‐catenin would seem to support a common clonal origin for the carcinomatous and sarcomatous components.</description><identifier>ISSN: 0303-6987</identifier><identifier>EISSN: 1600-0560</identifier><identifier>DOI: 10.1111/cup.13407</identifier><identifier>PMID: 30582193</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Case reports ; Cysts ; epidermal cyst ; Mitosis ; Nucleoli ; pilomatrical carcinosarcoma ; pilomatricoma</subject><ispartof>Journal of cutaneous pathology, 2019-04, Vol.46 (4), p.267-270</ispartof><rights>2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>This article is protected by copyright. All rights reserved.</rights><rights>2019 John Wiley & Sons A/S. 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This report describes the case of a 100‐year‐old woman with a mass on the left temple that had existed for several decades but had recently grown in size. Histology showed an asymmetric lesion composed of basaloid cells, spindle cells, and “shadow” or “ghost” cells. Cells had atypical hyperchromatic nuclei with prominent nucleoli, high mitotic activity, and atypical mitosis. In the central area, an epidermal cyst‐like structure was seen. The diagnosis of pilomatrical carcinosarcoma was rendered. This case appeared to have arisen from malignant transformation of a pilomatricoma because of the long clinical history and existence of a benign epidermal cyst‐like structure. In addition, the observation that the basaloid cells and spindle cells showed a gradual transition from one to the other and that both types were positive for β‐catenin would seem to support a common clonal origin for the carcinomatous and sarcomatous components.</description><subject>Case reports</subject><subject>Cysts</subject><subject>epidermal cyst</subject><subject>Mitosis</subject><subject>Nucleoli</subject><subject>pilomatrical carcinosarcoma</subject><subject>pilomatricoma</subject><issn>0303-6987</issn><issn>1600-0560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kD1PwzAQhi0EoqUw8AdQJCaGtOc4_ghbFfElVaIDnS3XsUWqpA52ItR_jyGFjVtOunv0nu5B6BrDHMda6KGbY5IDP0FTzABSoAxO0RQIkJQVgk_QRQg7AMwEo-doQoCKDBdkisS6blyrel9r1SRaeV3vXYgtDhNnk_7dJL1pu8bcJ8u4DybxpnO-v0RnVjXBXB37DG0eH97K53T1-vRSLlepJoLxlJMC24rrLaEZExpbYXjGLKusYWC3OcdUaU4EKFLlmFJjcsC8gorpnFekIDN0O-Z23n0MJvRy5wa_jydl_ABnvICcR-pupLR3IXhjZefrVvmDxCC_HcnoSP44iuzNMXHYtqb6I3-lRGAxAp91Yw7_J8lysx4jvwBcEm6H</recordid><startdate>201904</startdate><enddate>201904</enddate><creator>Mori, Daisuke</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><orcidid>https://orcid.org/0000-0002-9583-5929</orcidid></search><sort><creationdate>201904</creationdate><title>Pilomatrical carcinosarcoma of the temple: A case report</title><author>Mori, Daisuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3867-7391fd7cb35268c1f8e726f6dfe60fb4715ac7380a3d4155ee4017d0d6c47d393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Case reports</topic><topic>Cysts</topic><topic>epidermal cyst</topic><topic>Mitosis</topic><topic>Nucleoli</topic><topic>pilomatrical carcinosarcoma</topic><topic>pilomatricoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mori, Daisuke</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of cutaneous pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mori, Daisuke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pilomatrical carcinosarcoma of the temple: A case report</atitle><jtitle>Journal of cutaneous pathology</jtitle><addtitle>J Cutan Pathol</addtitle><date>2019-04</date><risdate>2019</risdate><volume>46</volume><issue>4</issue><spage>267</spage><epage>270</epage><pages>267-270</pages><issn>0303-6987</issn><eissn>1600-0560</eissn><abstract>Pilomatrical carcinosarcoma is a very rare entity, with only six cases reported until now. This report describes the case of a 100‐year‐old woman with a mass on the left temple that had existed for several decades but had recently grown in size. Histology showed an asymmetric lesion composed of basaloid cells, spindle cells, and “shadow” or “ghost” cells. Cells had atypical hyperchromatic nuclei with prominent nucleoli, high mitotic activity, and atypical mitosis. In the central area, an epidermal cyst‐like structure was seen. The diagnosis of pilomatrical carcinosarcoma was rendered. This case appeared to have arisen from malignant transformation of a pilomatricoma because of the long clinical history and existence of a benign epidermal cyst‐like structure. In addition, the observation that the basaloid cells and spindle cells showed a gradual transition from one to the other and that both types were positive for β‐catenin would seem to support a common clonal origin for the carcinomatous and sarcomatous components.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>30582193</pmid><doi>10.1111/cup.13407</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-9583-5929</orcidid></addata></record> |
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subjects | Case reports Cysts epidermal cyst Mitosis Nucleoli pilomatrical carcinosarcoma pilomatricoma |
title | Pilomatrical carcinosarcoma of the temple: A case report |
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