Sweat gland adenomas: Immunohistochemical study with emphasis on myoepithelial differentiation
Thirty‐one dermal appendage tumors of sweat gland differentiation including 7 spiradenomas (SPA), 8 cylindromas (CYL), 8 acrospiromas (ACS), and 8 chondroid syringomas (CS) were analyzed using antibodies to epithelial membrane antigen (EMA), cytokeratin (AE1, AE3, CAM 5.2, 34BE12), S‐100 protein, ac...
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description | Thirty‐one dermal appendage tumors of sweat gland differentiation including 7 spiradenomas (SPA), 8 cylindromas (CYL), 8 acrospiromas (ACS), and 8 chondroid syringomas (CS) were analyzed using antibodies to epithelial membrane antigen (EMA), cytokeratin (AE1, AE3, CAM 5.2, 34BE12), S‐100 protein, actin (ACT), and desmin (DBS) to characterize the immunocytochemical profile of benign sweat gland tumors. Cytokeratin expression was variable; AE1, 34BE12, AE3, and CAM 5.2 were present in 31, 24, 23, and 22 tumors respectively; 29 tumors contained EMA. Seventeen tumors, (6 SPA, 8 CYL, 2 ACS, 1 CS) stained with antibody to alpha smooth muscle actin, and 26 (7 SPA, 7 CYL, 4 ACS, 8 CS) expressed S‐100 protein. Although some prior studies had reported actin filaments on electron microscopy in both spiradenoma and cylindroma, these tumors have previously been considered to be negative for myoepithelial differentiation. All spiradenomas and cylindromas we studied demonstrated actin and/or S‐100 protein positivity in basal epithelial cells, consistent with myoepithelial differentiation. The organization of actin and S‐100 protein positivity displayed by the spiradenomas and cylindromas we studied suggests that the tumors are differentiated towards the secretory portion of the eccrine sweat gland. |
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Cytokeratin expression was variable; AE1, 34BE12, AE3, and CAM 5.2 were present in 31, 24, 23, and 22 tumors respectively; 29 tumors contained EMA. Seventeen tumors, (6 SPA, 8 CYL, 2 ACS, 1 CS) stained with antibody to alpha smooth muscle actin, and 26 (7 SPA, 7 CYL, 4 ACS, 8 CS) expressed S‐100 protein. Although some prior studies had reported actin filaments on electron microscopy in both spiradenoma and cylindroma, these tumors have previously been considered to be negative for myoepithelial differentiation. All spiradenomas and cylindromas we studied demonstrated actin and/or S‐100 protein positivity in basal epithelial cells, consistent with myoepithelial differentiation. The organization of actin and S‐100 protein positivity displayed by the spiradenomas and cylindromas we studied suggests that the tumors are differentiated towards the secretory portion of the eccrine sweat gland.</description><identifier>ISSN: 0303-6987</identifier><identifier>EISSN: 1600-0560</identifier><identifier>DOI: 10.1111/j.1600-0560.1993.tb01272.x</identifier><identifier>PMID: 7693778</identifier><identifier>CODEN: JCUPBN</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Acrospiroma - chemistry ; Acrospiroma - pathology ; Actins - analysis ; Actins - immunology ; Adenoma, Sweat Gland - chemistry ; Adenoma, Sweat Gland - pathology ; Biological and medical sciences ; Cell Transformation, Neoplastic - pathology ; Dermatology ; Desmin - analysis ; Desmin - immunology ; Epithelium - pathology ; Humans ; Immune Sera - immunology ; Immunohistochemistry ; Keratins - analysis ; Keratins - immunology ; Medical sciences ; Membrane Glycoproteins - analysis ; Membrane Glycoproteins - immunology ; Mucin-1 ; S100 Proteins - analysis ; S100 Proteins - immunology ; Sweat Gland Neoplasms - chemistry ; Sweat Gland Neoplasms - pathology ; Syringoma - chemistry ; Syringoma - pathology ; Tumors of the skin and soft tissue. Premalignant lesions</subject><ispartof>Journal of cutaneous pathology, 1993-08, Vol.20 (4), p.337-343</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4367-121bfcad07b00efd23296d3eb009956ed589708707876417cad111d1b4e331233</citedby><cites>FETCH-LOGICAL-c4367-121bfcad07b00efd23296d3eb009956ed589708707876417cad111d1b4e331233</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.1600-0560.1993.tb01272.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1600-0560.1993.tb01272.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4852218$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7693778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wiley, Elizabeth L.</creatorcontrib><creatorcontrib>Milchgrub, Sara</creatorcontrib><creatorcontrib>Freeman, Robert G.</creatorcontrib><creatorcontrib>Kim, Elizabeth S.</creatorcontrib><title>Sweat gland adenomas: Immunohistochemical study with emphasis on myoepithelial differentiation</title><title>Journal of cutaneous pathology</title><addtitle>J Cutan Pathol</addtitle><description>Thirty‐one dermal appendage tumors of sweat gland differentiation including 7 spiradenomas (SPA), 8 cylindromas (CYL), 8 acrospiromas (ACS), and 8 chondroid syringomas (CS) were analyzed using antibodies to epithelial membrane antigen (EMA), cytokeratin (AE1, AE3, CAM 5.2, 34BE12), S‐100 protein, actin (ACT), and desmin (DBS) to characterize the immunocytochemical profile of benign sweat gland tumors. Cytokeratin expression was variable; AE1, 34BE12, AE3, and CAM 5.2 were present in 31, 24, 23, and 22 tumors respectively; 29 tumors contained EMA. Seventeen tumors, (6 SPA, 8 CYL, 2 ACS, 1 CS) stained with antibody to alpha smooth muscle actin, and 26 (7 SPA, 7 CYL, 4 ACS, 8 CS) expressed S‐100 protein. Although some prior studies had reported actin filaments on electron microscopy in both spiradenoma and cylindroma, these tumors have previously been considered to be negative for myoepithelial differentiation. All spiradenomas and cylindromas we studied demonstrated actin and/or S‐100 protein positivity in basal epithelial cells, consistent with myoepithelial differentiation. The organization of actin and S‐100 protein positivity displayed by the spiradenomas and cylindromas we studied suggests that the tumors are differentiated towards the secretory portion of the eccrine sweat gland.</description><subject>Acrospiroma - chemistry</subject><subject>Acrospiroma - pathology</subject><subject>Actins - analysis</subject><subject>Actins - immunology</subject><subject>Adenoma, Sweat Gland - chemistry</subject><subject>Adenoma, Sweat Gland - pathology</subject><subject>Biological and medical sciences</subject><subject>Cell Transformation, Neoplastic - pathology</subject><subject>Dermatology</subject><subject>Desmin - analysis</subject><subject>Desmin - immunology</subject><subject>Epithelium - pathology</subject><subject>Humans</subject><subject>Immune Sera - immunology</subject><subject>Immunohistochemistry</subject><subject>Keratins - analysis</subject><subject>Keratins - immunology</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - analysis</subject><subject>Membrane Glycoproteins - immunology</subject><subject>Mucin-1</subject><subject>S100 Proteins - analysis</subject><subject>S100 Proteins - immunology</subject><subject>Sweat Gland Neoplasms - chemistry</subject><subject>Sweat Gland Neoplasms - pathology</subject><subject>Syringoma - chemistry</subject><subject>Syringoma - pathology</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0303-6987</issn><issn>1600-0560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkV1v0zAUhq0JNLqNn4AUIcRdij8SO97FJFSxDzSNDdh2N8uJT6i7OC5xorb_HkeNeo9vLJ_3Pe-xHyP0keA5ievLak44xinOeSxIyeZ9iQkVdL49QrOD9AbNMMMs5bIQ79BJCCuMCS94foyOBZdMiGKGXn5tQPfJn0a3JtEGWu90OE9unBtav7Sh99USnK10k4R-MLtkY_tlAm691MGGxLeJ23lYxyI0NpqMrWvooO2t7q1vz9DbWjcB3k_7KXq8_PZ7cZ3e_ri6WXy9TauMcZESSsq60gaLEmOoDWVUcsMgnqTMOZi8kAIXAotC8IyIaI0cDCkzYIxQxk7R533uuvN_Bwi9cjZU0MRngR-CEhzHQZmMxvO9sep8CB3Uat1Zp7udIliNcNVKjQTVSFCNcNUEV21j84dpylA6MIfWiWbUP026DpFY3em2suFgy4qcUjLaLva2jW1g9x8XUIvHe8ZEDEj3AfF_YHsI0N2r4oKJXD3fXanr7w8_2cPdk6LsH9HYppQ</recordid><startdate>199308</startdate><enddate>199308</enddate><creator>Wiley, Elizabeth L.</creator><creator>Milchgrub, Sara</creator><creator>Freeman, Robert G.</creator><creator>Kim, Elizabeth S.</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>199308</creationdate><title>Sweat gland adenomas: Immunohistochemical study with emphasis on myoepithelial differentiation</title><author>Wiley, Elizabeth L. ; Milchgrub, Sara ; Freeman, Robert G. ; Kim, Elizabeth S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4367-121bfcad07b00efd23296d3eb009956ed589708707876417cad111d1b4e331233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Acrospiroma - chemistry</topic><topic>Acrospiroma - pathology</topic><topic>Actins - analysis</topic><topic>Actins - immunology</topic><topic>Adenoma, Sweat Gland - chemistry</topic><topic>Adenoma, Sweat Gland - pathology</topic><topic>Biological and medical sciences</topic><topic>Cell Transformation, Neoplastic - pathology</topic><topic>Dermatology</topic><topic>Desmin - analysis</topic><topic>Desmin - immunology</topic><topic>Epithelium - pathology</topic><topic>Humans</topic><topic>Immune Sera - immunology</topic><topic>Immunohistochemistry</topic><topic>Keratins - analysis</topic><topic>Keratins - immunology</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins - analysis</topic><topic>Membrane Glycoproteins - immunology</topic><topic>Mucin-1</topic><topic>S100 Proteins - analysis</topic><topic>S100 Proteins - immunology</topic><topic>Sweat Gland Neoplasms - chemistry</topic><topic>Sweat Gland Neoplasms - pathology</topic><topic>Syringoma - chemistry</topic><topic>Syringoma - pathology</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wiley, Elizabeth L.</creatorcontrib><creatorcontrib>Milchgrub, Sara</creatorcontrib><creatorcontrib>Freeman, Robert G.</creatorcontrib><creatorcontrib>Kim, Elizabeth S.</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>Journal of cutaneous pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wiley, Elizabeth L.</au><au>Milchgrub, Sara</au><au>Freeman, Robert G.</au><au>Kim, Elizabeth S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sweat gland adenomas: Immunohistochemical study with emphasis on myoepithelial differentiation</atitle><jtitle>Journal of cutaneous pathology</jtitle><addtitle>J Cutan Pathol</addtitle><date>1993-08</date><risdate>1993</risdate><volume>20</volume><issue>4</issue><spage>337</spage><epage>343</epage><pages>337-343</pages><issn>0303-6987</issn><eissn>1600-0560</eissn><coden>JCUPBN</coden><abstract>Thirty‐one dermal appendage tumors of sweat gland differentiation including 7 spiradenomas (SPA), 8 cylindromas (CYL), 8 acrospiromas (ACS), and 8 chondroid syringomas (CS) were analyzed using antibodies to epithelial membrane antigen (EMA), cytokeratin (AE1, AE3, CAM 5.2, 34BE12), S‐100 protein, actin (ACT), and desmin (DBS) to characterize the immunocytochemical profile of benign sweat gland tumors. Cytokeratin expression was variable; AE1, 34BE12, AE3, and CAM 5.2 were present in 31, 24, 23, and 22 tumors respectively; 29 tumors contained EMA. Seventeen tumors, (6 SPA, 8 CYL, 2 ACS, 1 CS) stained with antibody to alpha smooth muscle actin, and 26 (7 SPA, 7 CYL, 4 ACS, 8 CS) expressed S‐100 protein. Although some prior studies had reported actin filaments on electron microscopy in both spiradenoma and cylindroma, these tumors have previously been considered to be negative for myoepithelial differentiation. All spiradenomas and cylindromas we studied demonstrated actin and/or S‐100 protein positivity in basal epithelial cells, consistent with myoepithelial differentiation. The organization of actin and S‐100 protein positivity displayed by the spiradenomas and cylindromas we studied suggests that the tumors are differentiated towards the secretory portion of the eccrine sweat gland.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>7693778</pmid><doi>10.1111/j.1600-0560.1993.tb01272.x</doi><tpages>7</tpages></addata></record> |
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subjects | Acrospiroma - chemistry Acrospiroma - pathology Actins - analysis Actins - immunology Adenoma, Sweat Gland - chemistry Adenoma, Sweat Gland - pathology Biological and medical sciences Cell Transformation, Neoplastic - pathology Dermatology Desmin - analysis Desmin - immunology Epithelium - pathology Humans Immune Sera - immunology Immunohistochemistry Keratins - analysis Keratins - immunology Medical sciences Membrane Glycoproteins - analysis Membrane Glycoproteins - immunology Mucin-1 S100 Proteins - analysis S100 Proteins - immunology Sweat Gland Neoplasms - chemistry Sweat Gland Neoplasms - pathology Syringoma - chemistry Syringoma - pathology Tumors of the skin and soft tissue. Premalignant lesions |
title | Sweat gland adenomas: Immunohistochemical study with emphasis on myoepithelial differentiation |
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