Pseudoangiosarcomatous carcinoma: a clinicopathological study of seven cases
Seven cases of carcinoma mimicking angiosarcoma occurring in skin (3 cases), breast (3) and lung (1) are described. The cutaneous, pulmonary and one of the breast carcinomas were poorly differentiated and squamous in type; the other two breast tumours were poorly differentiated ductal carcinomas wit...
Gespeichert in:
Veröffentlicht in: | Histopathology 1992-07, Vol.21 (1), p.13-23 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 23 |
---|---|
container_issue | 1 |
container_start_page | 13 |
container_title | Histopathology |
container_volume | 21 |
creator | BANERJEE, S.S. EYDEN, B.P. WELLS, S. McWILLIAM, L.J. HARRIS, M. |
description | Seven cases of carcinoma mimicking angiosarcoma occurring in skin (3 cases), breast (3) and lung (1) are described. The cutaneous, pulmonary and one of the breast carcinomas were poorly differentiated and squamous in type; the other two breast tumours were poorly differentiated ductal carcinomas with focal squamous differentiation. Histologically, the pseudoangiosarcomatous pattern was due to complex anastomosing channels and spaces lined by neoplastic cells. The spaces contained hyaluronic acid. The neoplastic cells exhibited cytokeratin positivity but yielded negative results with the endothelial cell markers, factor VIII‐related antigen and CD 34 (QB‐END/10). Two breast tumours showed binding of UEA‐1. Ultrastructurally, unequivocal epithelial differentiation was demonstrated in six of the cases. Pathogenetically, these tumours appeared to be variants of acantholytic squamous cell carcinoma. Recognition of this unusual form of carcinoma is important, as an incorrect diagnosis of angiosarcoma may lead to inappropriate treatment and prognostication. |
doi_str_mv | 10.1111/j.1365-2559.1992.tb00338.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73078909</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73078909</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3503-41da8d4f97261ca70a580b25f37b837cdd898da85a53a2830ef8b3d317fe72373</originalsourceid><addsrcrecordid>eNqVkF2P1CAUhonRrLOrP8GkMca7VuCUApt4sVndD3eixo94SSilK2OnjD3tOvPvZdLJeC03QN7nhZOHkJeMFiytN6uCQSVyLoQumNa8GGtKAVSxfUQWx-gxWVCgOqeskk_JKeKKUiaB8xNywioomVYLsvyMfmqi7e9DRDu4uLZjnDBz6Rz6dDvPbOa60AcXN3b8Gbt4H5ztMhynZpfFNkP_4PvEo8dn5ElrO_TPD_sZ-X71_tvlTb78dH17ebHMHQgKeckaq5qy1ZJXzFlJrVC05qIFWSuQrmmUVgkRVoDlCqhvVQ0NMNl6yUHCGXk9v7sZ4u_J42jWAZ3vOtv7NLyRQKXSVCfwfAbdEBEH35rNENZ22BlGzV6lWZm9L7P3ZfYqzUGl2abyi8MvU732zb_q7C7lrw65xWSkHWzvAh4xIXgpOEvY2xn7Ezq_-48BzM3tVwapn8_9gKPfHvt2-GUqCVKYHx-vzRf4UNK7qzvzDv4CC2ef1w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73078909</pqid></control><display><type>article</type><title>Pseudoangiosarcomatous carcinoma: a clinicopathological study of seven cases</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><creator>BANERJEE, S.S. ; EYDEN, B.P. ; WELLS, S. ; McWILLIAM, L.J. ; HARRIS, M.</creator><creatorcontrib>BANERJEE, S.S. ; EYDEN, B.P. ; WELLS, S. ; McWILLIAM, L.J. ; HARRIS, M.</creatorcontrib><description>Seven cases of carcinoma mimicking angiosarcoma occurring in skin (3 cases), breast (3) and lung (1) are described. The cutaneous, pulmonary and one of the breast carcinomas were poorly differentiated and squamous in type; the other two breast tumours were poorly differentiated ductal carcinomas with focal squamous differentiation. Histologically, the pseudoangiosarcomatous pattern was due to complex anastomosing channels and spaces lined by neoplastic cells. The spaces contained hyaluronic acid. The neoplastic cells exhibited cytokeratin positivity but yielded negative results with the endothelial cell markers, factor VIII‐related antigen and CD 34 (QB‐END/10). Two breast tumours showed binding of UEA‐1. Ultrastructurally, unequivocal epithelial differentiation was demonstrated in six of the cases. Pathogenetically, these tumours appeared to be variants of acantholytic squamous cell carcinoma. Recognition of this unusual form of carcinoma is important, as an incorrect diagnosis of angiosarcoma may lead to inappropriate treatment and prognostication.</description><identifier>ISSN: 0309-0167</identifier><identifier>EISSN: 1365-2559</identifier><identifier>DOI: 10.1111/j.1365-2559.1992.tb00338.x</identifier><identifier>PMID: 1634198</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Aged, 80 and over ; Biological and medical sciences ; breast ; Breast Neoplasms - pathology ; Breast Neoplasms - ultrastructure ; Dermatology ; Diagnosis, Differential ; Female ; Hemangiosarcoma - pathology ; Hemangiosarcoma - ultrastructure ; Histocytochemistry ; Humans ; Immunoenzyme Techniques ; immunohistochemistry ; keywords ; light microscopy ; lung ; Lung Neoplasms - pathology ; Lung Neoplasms - ultrastructure ; Male ; Medical sciences ; Middle Aged ; pseudoangiosarcomatous carcinoma ; skin ; Skin Neoplasms - pathology ; Skin Neoplasms - ultrastructure ; Tumors of the skin and soft tissue. Premalignant lesions ; ultrastructure</subject><ispartof>Histopathology, 1992-07, Vol.21 (1), p.13-23</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3503-41da8d4f97261ca70a580b25f37b837cdd898da85a53a2830ef8b3d317fe72373</citedby><cites>FETCH-LOGICAL-c3503-41da8d4f97261ca70a580b25f37b837cdd898da85a53a2830ef8b3d317fe72373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2559.1992.tb00338.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2559.1992.tb00338.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5524521$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1634198$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BANERJEE, S.S.</creatorcontrib><creatorcontrib>EYDEN, B.P.</creatorcontrib><creatorcontrib>WELLS, S.</creatorcontrib><creatorcontrib>McWILLIAM, L.J.</creatorcontrib><creatorcontrib>HARRIS, M.</creatorcontrib><title>Pseudoangiosarcomatous carcinoma: a clinicopathological study of seven cases</title><title>Histopathology</title><addtitle>Histopathology</addtitle><description>Seven cases of carcinoma mimicking angiosarcoma occurring in skin (3 cases), breast (3) and lung (1) are described. The cutaneous, pulmonary and one of the breast carcinomas were poorly differentiated and squamous in type; the other two breast tumours were poorly differentiated ductal carcinomas with focal squamous differentiation. Histologically, the pseudoangiosarcomatous pattern was due to complex anastomosing channels and spaces lined by neoplastic cells. The spaces contained hyaluronic acid. The neoplastic cells exhibited cytokeratin positivity but yielded negative results with the endothelial cell markers, factor VIII‐related antigen and CD 34 (QB‐END/10). Two breast tumours showed binding of UEA‐1. Ultrastructurally, unequivocal epithelial differentiation was demonstrated in six of the cases. Pathogenetically, these tumours appeared to be variants of acantholytic squamous cell carcinoma. Recognition of this unusual form of carcinoma is important, as an incorrect diagnosis of angiosarcoma may lead to inappropriate treatment and prognostication.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>breast</subject><subject>Breast Neoplasms - pathology</subject><subject>Breast Neoplasms - ultrastructure</subject><subject>Dermatology</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Hemangiosarcoma - pathology</subject><subject>Hemangiosarcoma - ultrastructure</subject><subject>Histocytochemistry</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>immunohistochemistry</subject><subject>keywords</subject><subject>light microscopy</subject><subject>lung</subject><subject>Lung Neoplasms - pathology</subject><subject>Lung Neoplasms - ultrastructure</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>pseudoangiosarcomatous carcinoma</subject><subject>skin</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - ultrastructure</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><subject>ultrastructure</subject><issn>0309-0167</issn><issn>1365-2559</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkF2P1CAUhonRrLOrP8GkMca7VuCUApt4sVndD3eixo94SSilK2OnjD3tOvPvZdLJeC03QN7nhZOHkJeMFiytN6uCQSVyLoQumNa8GGtKAVSxfUQWx-gxWVCgOqeskk_JKeKKUiaB8xNywioomVYLsvyMfmqi7e9DRDu4uLZjnDBz6Rz6dDvPbOa60AcXN3b8Gbt4H5ztMhynZpfFNkP_4PvEo8dn5ElrO_TPD_sZ-X71_tvlTb78dH17ebHMHQgKeckaq5qy1ZJXzFlJrVC05qIFWSuQrmmUVgkRVoDlCqhvVQ0NMNl6yUHCGXk9v7sZ4u_J42jWAZ3vOtv7NLyRQKXSVCfwfAbdEBEH35rNENZ22BlGzV6lWZm9L7P3ZfYqzUGl2abyi8MvU732zb_q7C7lrw65xWSkHWzvAh4xIXgpOEvY2xn7Ezq_-48BzM3tVwapn8_9gKPfHvt2-GUqCVKYHx-vzRf4UNK7qzvzDv4CC2ef1w</recordid><startdate>199207</startdate><enddate>199207</enddate><creator>BANERJEE, S.S.</creator><creator>EYDEN, B.P.</creator><creator>WELLS, S.</creator><creator>McWILLIAM, L.J.</creator><creator>HARRIS, M.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><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>199207</creationdate><title>Pseudoangiosarcomatous carcinoma: a clinicopathological study of seven cases</title><author>BANERJEE, S.S. ; EYDEN, B.P. ; WELLS, S. ; McWILLIAM, L.J. ; HARRIS, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3503-41da8d4f97261ca70a580b25f37b837cdd898da85a53a2830ef8b3d317fe72373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>breast</topic><topic>Breast Neoplasms - pathology</topic><topic>Breast Neoplasms - ultrastructure</topic><topic>Dermatology</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Hemangiosarcoma - pathology</topic><topic>Hemangiosarcoma - ultrastructure</topic><topic>Histocytochemistry</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>immunohistochemistry</topic><topic>keywords</topic><topic>light microscopy</topic><topic>lung</topic><topic>Lung Neoplasms - pathology</topic><topic>Lung Neoplasms - ultrastructure</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>pseudoangiosarcomatous carcinoma</topic><topic>skin</topic><topic>Skin Neoplasms - pathology</topic><topic>Skin Neoplasms - ultrastructure</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><topic>ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BANERJEE, S.S.</creatorcontrib><creatorcontrib>EYDEN, B.P.</creatorcontrib><creatorcontrib>WELLS, S.</creatorcontrib><creatorcontrib>McWILLIAM, L.J.</creatorcontrib><creatorcontrib>HARRIS, M.</creatorcontrib><collection>Istex</collection><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>Histopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BANERJEE, S.S.</au><au>EYDEN, B.P.</au><au>WELLS, S.</au><au>McWILLIAM, L.J.</au><au>HARRIS, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pseudoangiosarcomatous carcinoma: a clinicopathological study of seven cases</atitle><jtitle>Histopathology</jtitle><addtitle>Histopathology</addtitle><date>1992-07</date><risdate>1992</risdate><volume>21</volume><issue>1</issue><spage>13</spage><epage>23</epage><pages>13-23</pages><issn>0309-0167</issn><eissn>1365-2559</eissn><abstract>Seven cases of carcinoma mimicking angiosarcoma occurring in skin (3 cases), breast (3) and lung (1) are described. The cutaneous, pulmonary and one of the breast carcinomas were poorly differentiated and squamous in type; the other two breast tumours were poorly differentiated ductal carcinomas with focal squamous differentiation. Histologically, the pseudoangiosarcomatous pattern was due to complex anastomosing channels and spaces lined by neoplastic cells. The spaces contained hyaluronic acid. The neoplastic cells exhibited cytokeratin positivity but yielded negative results with the endothelial cell markers, factor VIII‐related antigen and CD 34 (QB‐END/10). Two breast tumours showed binding of UEA‐1. Ultrastructurally, unequivocal epithelial differentiation was demonstrated in six of the cases. Pathogenetically, these tumours appeared to be variants of acantholytic squamous cell carcinoma. Recognition of this unusual form of carcinoma is important, as an incorrect diagnosis of angiosarcoma may lead to inappropriate treatment and prognostication.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1634198</pmid><doi>10.1111/j.1365-2559.1992.tb00338.x</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0309-0167 |
ispartof | Histopathology, 1992-07, Vol.21 (1), p.13-23 |
issn | 0309-0167 1365-2559 |
language | eng |
recordid | cdi_proquest_miscellaneous_73078909 |
source | MEDLINE; Wiley Online Library All Journals |
subjects | Aged Aged, 80 and over Biological and medical sciences breast Breast Neoplasms - pathology Breast Neoplasms - ultrastructure Dermatology Diagnosis, Differential Female Hemangiosarcoma - pathology Hemangiosarcoma - ultrastructure Histocytochemistry Humans Immunoenzyme Techniques immunohistochemistry keywords light microscopy lung Lung Neoplasms - pathology Lung Neoplasms - ultrastructure Male Medical sciences Middle Aged pseudoangiosarcomatous carcinoma skin Skin Neoplasms - pathology Skin Neoplasms - ultrastructure Tumors of the skin and soft tissue. Premalignant lesions ultrastructure |
title | Pseudoangiosarcomatous carcinoma: a clinicopathological study of seven cases |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T13%3A30%3A02IST&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=Pseudoangiosarcomatous%20carcinoma:%20a%20clinicopathological%20study%20of%20seven%20cases&rft.jtitle=Histopathology&rft.au=BANERJEE,%20S.S.&rft.date=1992-07&rft.volume=21&rft.issue=1&rft.spage=13&rft.epage=23&rft.pages=13-23&rft.issn=0309-0167&rft.eissn=1365-2559&rft_id=info:doi/10.1111/j.1365-2559.1992.tb00338.x&rft_dat=%3Cproquest_cross%3E73078909%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=73078909&rft_id=info:pmid/1634198&rfr_iscdi=true |