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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of cutaneous pathology 2019-04, Vol.46 (4), p.267-270
1. Verfasser: Mori, Daisuke
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 270
container_issue 4
container_start_page 267
container_title Journal of cutaneous pathology
container_volume 46
creator Mori, Daisuke
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.
doi_str_mv 10.1111/cup.13407
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2191279047</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2191279047</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3867-7391fd7cb35268c1f8e726f6dfe60fb4715ac7380a3d4155ee4017d0d6c47d393</originalsourceid><addsrcrecordid>eNp1kD1PwzAQhi0EoqUw8AdQJCaGtOc4_ghbFfElVaIDnS3XsUWqpA52ItR_jyGFjVtOunv0nu5B6BrDHMda6KGbY5IDP0FTzABSoAxO0RQIkJQVgk_QRQg7AMwEo-doQoCKDBdkisS6blyrel9r1SRaeV3vXYgtDhNnk_7dJL1pu8bcJ8u4DybxpnO-v0RnVjXBXB37DG0eH97K53T1-vRSLlepJoLxlJMC24rrLaEZExpbYXjGLKusYWC3OcdUaU4EKFLlmFJjcsC8gorpnFekIDN0O-Z23n0MJvRy5wa_jydl_ABnvICcR-pupLR3IXhjZefrVvmDxCC_HcnoSP44iuzNMXHYtqb6I3-lRGAxAp91Yw7_J8lysx4jvwBcEm6H</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2191279047</pqid></control><display><type>article</type><title>Pilomatrical carcinosarcoma of the temple: A case report</title><source>Wiley-Blackwell Journals</source><creator>Mori, Daisuke</creator><creatorcontrib>Mori, Daisuke</creatorcontrib><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.</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 &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><rights>This article is protected by copyright. All rights reserved.</rights><rights>2019 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3867-7391fd7cb35268c1f8e726f6dfe60fb4715ac7380a3d4155ee4017d0d6c47d393</citedby><cites>FETCH-LOGICAL-c3867-7391fd7cb35268c1f8e726f6dfe60fb4715ac7380a3d4155ee4017d0d6c47d393</cites><orcidid>0000-0002-9583-5929</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcup.13407$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcup.13407$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30582193$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mori, Daisuke</creatorcontrib><title>Pilomatrical carcinosarcoma of the temple: A case report</title><title>Journal of cutaneous pathology</title><addtitle>J Cutan Pathol</addtitle><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.</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>
fulltext fulltext
identifier ISSN: 0303-6987
ispartof Journal of cutaneous pathology, 2019-04, Vol.46 (4), p.267-270
issn 0303-6987
1600-0560
language eng
recordid cdi_proquest_journals_2191279047
source Wiley-Blackwell Journals
subjects Case reports
Cysts
epidermal cyst
Mitosis
Nucleoli
pilomatrical carcinosarcoma
pilomatricoma
title Pilomatrical carcinosarcoma of the temple: A case report
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T19%3A01%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pilomatrical%20carcinosarcoma%20of%20the%20temple:%20A%20case%20report&rft.jtitle=Journal%20of%20cutaneous%20pathology&rft.au=Mori,%20Daisuke&rft.date=2019-04&rft.volume=46&rft.issue=4&rft.spage=267&rft.epage=270&rft.pages=267-270&rft.issn=0303-6987&rft.eissn=1600-0560&rft_id=info:doi/10.1111/cup.13407&rft_dat=%3Cproquest_cross%3E2191279047%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2191279047&rft_id=info:pmid/30582193&rfr_iscdi=true