Loading…

Pericyte Antigens in Perivascular Soft Tissue Tumors

Introduction. Perivascular soft tissue tumors are relatively uncommon neoplasms of unclear line of differentiation, although most are presumed to originate from pericytes or modified perivascular cells. Among these, glomus tumor, myopericytoma, and angioleiomyoma share a spectrum of histologic findi...

Full description

Saved in:
Bibliographic Details
Published in:International journal of surgical pathology 2015-12, Vol.23 (8), p.638-648
Main Authors: Shen, Jia, Shrestha, Swati, Yen, Yu-Hsin, Asatrian, Greg, Mravic, Marco, Soo, Chia, Ting, Kang, Dry, Sarah M., Peault, Bruno, James, Aaron W.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c500t-306263ace2f0ae6ebd317f58c96a399c564fb4533a7b709121bec06a67a203c93
cites cdi_FETCH-LOGICAL-c500t-306263ace2f0ae6ebd317f58c96a399c564fb4533a7b709121bec06a67a203c93
container_end_page 648
container_issue 8
container_start_page 638
container_title International journal of surgical pathology
container_volume 23
creator Shen, Jia
Shrestha, Swati
Yen, Yu-Hsin
Asatrian, Greg
Mravic, Marco
Soo, Chia
Ting, Kang
Dry, Sarah M.
Peault, Bruno
James, Aaron W.
description Introduction. Perivascular soft tissue tumors are relatively uncommon neoplasms of unclear line of differentiation, although most are presumed to originate from pericytes or modified perivascular cells. Among these, glomus tumor, myopericytoma, and angioleiomyoma share a spectrum of histologic findings and a perivascular growth pattern. In contrast, solitary fibrous tumor (previously termed hemangiopericytoma) was once hypothesized to have pericytic differentiation. Methods. Here, we systematically examine pericyte immunohistochemical markers among glomus tumor (including malignant glomus tumor), myopericytoma, angioleiomyoma, and solitary fibrous tumor. Immunohistochemical staining and semiquantification was performed using well-defined pericyte antigens, including αSMA, CD146, and PDGFRβ. Results. Glomus tumor and myopericytoma demonstrate diffuse staining for all pericyte markers, including immunohistochemical reactivity for αSMA, CD146, and PDGFRβ. Malignant glomus tumors all showed some degree of pericyte marker immunoreactivity, although it was significantly reduced. Angioleiomyoma shared a similar αSMA + CD146 + PDGFRβ+ immunophenotype; however, this was predominantly seen in the areas of perivascular tumor growth. Solitary fibrous tumors showed patchy PDGFRβ immunoreactivity only. Discussion. In summary, pericyte marker expression is a ubiquitous finding in glomus tumor, myopericytoma, and angioleiomyoma. Malignant glomus tumor shows a comparative reduction in pericyte marker expression, which may represent partial loss of pericytic differentiation. Pericyte markers are essentially not seen in solitary fibrous tumor. The combination of αSMA, CD146, and PDGFRβ immunohistochemical stainings may be of utility for the evaluation of pericytic differentiation in soft tissue tumors.
doi_str_mv 10.1177/1066896915591272
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4641786</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_1066896915591272</sage_id><sourcerecordid>1732599992</sourcerecordid><originalsourceid>FETCH-LOGICAL-c500t-306263ace2f0ae6ebd317f58c96a399c564fb4533a7b709121bec06a67a203c93</originalsourceid><addsrcrecordid>eNp1UE1LAzEQDaLYWr17kj16WZ0km2RzEUrxCwoK1nPIptmash812S3035vSWlRwLjPMe_Nm5iF0ieEGYyFuMXCeSy4xYxITQY7QEMsMUpJxdhzrCKdbfIDOQlgCAOEEn6IB4ZAznokhyl6td2bT2WTcdG5hm5C4Jtk21zqYvtI-eWvLLpm5EHqbzPq69eEcnZS6CvZin0fo_eF-NnlKpy-Pz5PxNDUMoEspcMKpNpaUoC23xZxiUbLcSK6plCZeUBYZo1SLQkB8ABfWANdcaALUSDpCdzvdVV_Udm5s03ldqZV3tfYb1WqnfiON-1CLdq0ynmGR8yhwvRfw7WdvQ6dqF4ytKt3Ytg8KC0qYjEEiFXZU49sQvC0PazCordnqr9lx5OrneYeBb3cjId0Rgl5YtWx730S7_hf8Aq5ThuI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1732599992</pqid></control><display><type>article</type><title>Pericyte Antigens in Perivascular Soft Tissue Tumors</title><source>SAGE:Jisc Collections:SAGE Journals Read and Publish 2023-2024:2025 extension (reading list)</source><creator>Shen, Jia ; Shrestha, Swati ; Yen, Yu-Hsin ; Asatrian, Greg ; Mravic, Marco ; Soo, Chia ; Ting, Kang ; Dry, Sarah M. ; Peault, Bruno ; James, Aaron W.</creator><creatorcontrib>Shen, Jia ; Shrestha, Swati ; Yen, Yu-Hsin ; Asatrian, Greg ; Mravic, Marco ; Soo, Chia ; Ting, Kang ; Dry, Sarah M. ; Peault, Bruno ; James, Aaron W.</creatorcontrib><description>Introduction. Perivascular soft tissue tumors are relatively uncommon neoplasms of unclear line of differentiation, although most are presumed to originate from pericytes or modified perivascular cells. Among these, glomus tumor, myopericytoma, and angioleiomyoma share a spectrum of histologic findings and a perivascular growth pattern. In contrast, solitary fibrous tumor (previously termed hemangiopericytoma) was once hypothesized to have pericytic differentiation. Methods. Here, we systematically examine pericyte immunohistochemical markers among glomus tumor (including malignant glomus tumor), myopericytoma, angioleiomyoma, and solitary fibrous tumor. Immunohistochemical staining and semiquantification was performed using well-defined pericyte antigens, including αSMA, CD146, and PDGFRβ. Results. Glomus tumor and myopericytoma demonstrate diffuse staining for all pericyte markers, including immunohistochemical reactivity for αSMA, CD146, and PDGFRβ. Malignant glomus tumors all showed some degree of pericyte marker immunoreactivity, although it was significantly reduced. Angioleiomyoma shared a similar αSMA + CD146 + PDGFRβ+ immunophenotype; however, this was predominantly seen in the areas of perivascular tumor growth. Solitary fibrous tumors showed patchy PDGFRβ immunoreactivity only. Discussion. In summary, pericyte marker expression is a ubiquitous finding in glomus tumor, myopericytoma, and angioleiomyoma. Malignant glomus tumor shows a comparative reduction in pericyte marker expression, which may represent partial loss of pericytic differentiation. Pericyte markers are essentially not seen in solitary fibrous tumor. The combination of αSMA, CD146, and PDGFRβ immunohistochemical stainings may be of utility for the evaluation of pericytic differentiation in soft tissue tumors.</description><identifier>ISSN: 1066-8969</identifier><identifier>EISSN: 1940-2465</identifier><identifier>DOI: 10.1177/1066896915591272</identifier><identifier>PMID: 26085647</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Antigens, Neoplasm - analysis ; Antigens, Neoplasm - biosynthesis ; Biomarkers, Tumor - analysis ; Humans ; Immunohistochemistry ; Pericytes - metabolism ; Pericytes - pathology ; Retrospective Studies ; Soft Tissue Neoplasms - metabolism ; Soft Tissue Neoplasms - pathology</subject><ispartof>International journal of surgical pathology, 2015-12, Vol.23 (8), p.638-648</ispartof><rights>The Author(s) 2015</rights><rights>The Author(s) 2015.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c500t-306263ace2f0ae6ebd317f58c96a399c564fb4533a7b709121bec06a67a203c93</citedby><cites>FETCH-LOGICAL-c500t-306263ace2f0ae6ebd317f58c96a399c564fb4533a7b709121bec06a67a203c93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26085647$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shen, Jia</creatorcontrib><creatorcontrib>Shrestha, Swati</creatorcontrib><creatorcontrib>Yen, Yu-Hsin</creatorcontrib><creatorcontrib>Asatrian, Greg</creatorcontrib><creatorcontrib>Mravic, Marco</creatorcontrib><creatorcontrib>Soo, Chia</creatorcontrib><creatorcontrib>Ting, Kang</creatorcontrib><creatorcontrib>Dry, Sarah M.</creatorcontrib><creatorcontrib>Peault, Bruno</creatorcontrib><creatorcontrib>James, Aaron W.</creatorcontrib><title>Pericyte Antigens in Perivascular Soft Tissue Tumors</title><title>International journal of surgical pathology</title><addtitle>Int J Surg Pathol</addtitle><description>Introduction. Perivascular soft tissue tumors are relatively uncommon neoplasms of unclear line of differentiation, although most are presumed to originate from pericytes or modified perivascular cells. Among these, glomus tumor, myopericytoma, and angioleiomyoma share a spectrum of histologic findings and a perivascular growth pattern. In contrast, solitary fibrous tumor (previously termed hemangiopericytoma) was once hypothesized to have pericytic differentiation. Methods. Here, we systematically examine pericyte immunohistochemical markers among glomus tumor (including malignant glomus tumor), myopericytoma, angioleiomyoma, and solitary fibrous tumor. Immunohistochemical staining and semiquantification was performed using well-defined pericyte antigens, including αSMA, CD146, and PDGFRβ. Results. Glomus tumor and myopericytoma demonstrate diffuse staining for all pericyte markers, including immunohistochemical reactivity for αSMA, CD146, and PDGFRβ. Malignant glomus tumors all showed some degree of pericyte marker immunoreactivity, although it was significantly reduced. Angioleiomyoma shared a similar αSMA + CD146 + PDGFRβ+ immunophenotype; however, this was predominantly seen in the areas of perivascular tumor growth. Solitary fibrous tumors showed patchy PDGFRβ immunoreactivity only. Discussion. In summary, pericyte marker expression is a ubiquitous finding in glomus tumor, myopericytoma, and angioleiomyoma. Malignant glomus tumor shows a comparative reduction in pericyte marker expression, which may represent partial loss of pericytic differentiation. Pericyte markers are essentially not seen in solitary fibrous tumor. The combination of αSMA, CD146, and PDGFRβ immunohistochemical stainings may be of utility for the evaluation of pericytic differentiation in soft tissue tumors.</description><subject>Antigens, Neoplasm - analysis</subject><subject>Antigens, Neoplasm - biosynthesis</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Pericytes - metabolism</subject><subject>Pericytes - pathology</subject><subject>Retrospective Studies</subject><subject>Soft Tissue Neoplasms - metabolism</subject><subject>Soft Tissue Neoplasms - pathology</subject><issn>1066-8969</issn><issn>1940-2465</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp1UE1LAzEQDaLYWr17kj16WZ0km2RzEUrxCwoK1nPIptmash812S3035vSWlRwLjPMe_Nm5iF0ieEGYyFuMXCeSy4xYxITQY7QEMsMUpJxdhzrCKdbfIDOQlgCAOEEn6IB4ZAznokhyl6td2bT2WTcdG5hm5C4Jtk21zqYvtI-eWvLLpm5EHqbzPq69eEcnZS6CvZin0fo_eF-NnlKpy-Pz5PxNDUMoEspcMKpNpaUoC23xZxiUbLcSK6plCZeUBYZo1SLQkB8ABfWANdcaALUSDpCdzvdVV_Udm5s03ldqZV3tfYb1WqnfiON-1CLdq0ynmGR8yhwvRfw7WdvQ6dqF4ytKt3Ytg8KC0qYjEEiFXZU49sQvC0PazCordnqr9lx5OrneYeBb3cjId0Rgl5YtWx730S7_hf8Aq5ThuI</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Shen, Jia</creator><creator>Shrestha, Swati</creator><creator>Yen, Yu-Hsin</creator><creator>Asatrian, Greg</creator><creator>Mravic, Marco</creator><creator>Soo, Chia</creator><creator>Ting, Kang</creator><creator>Dry, Sarah M.</creator><creator>Peault, Bruno</creator><creator>James, Aaron W.</creator><general>SAGE Publications</general><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><scope>5PM</scope></search><sort><creationdate>20151201</creationdate><title>Pericyte Antigens in Perivascular Soft Tissue Tumors</title><author>Shen, Jia ; Shrestha, Swati ; Yen, Yu-Hsin ; Asatrian, Greg ; Mravic, Marco ; Soo, Chia ; Ting, Kang ; Dry, Sarah M. ; Peault, Bruno ; James, Aaron W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-306263ace2f0ae6ebd317f58c96a399c564fb4533a7b709121bec06a67a203c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Antigens, Neoplasm - analysis</topic><topic>Antigens, Neoplasm - biosynthesis</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Pericytes - metabolism</topic><topic>Pericytes - pathology</topic><topic>Retrospective Studies</topic><topic>Soft Tissue Neoplasms - metabolism</topic><topic>Soft Tissue Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Jia</creatorcontrib><creatorcontrib>Shrestha, Swati</creatorcontrib><creatorcontrib>Yen, Yu-Hsin</creatorcontrib><creatorcontrib>Asatrian, Greg</creatorcontrib><creatorcontrib>Mravic, Marco</creatorcontrib><creatorcontrib>Soo, Chia</creatorcontrib><creatorcontrib>Ting, Kang</creatorcontrib><creatorcontrib>Dry, Sarah M.</creatorcontrib><creatorcontrib>Peault, Bruno</creatorcontrib><creatorcontrib>James, Aaron W.</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of surgical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Jia</au><au>Shrestha, Swati</au><au>Yen, Yu-Hsin</au><au>Asatrian, Greg</au><au>Mravic, Marco</au><au>Soo, Chia</au><au>Ting, Kang</au><au>Dry, Sarah M.</au><au>Peault, Bruno</au><au>James, Aaron W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pericyte Antigens in Perivascular Soft Tissue Tumors</atitle><jtitle>International journal of surgical pathology</jtitle><addtitle>Int J Surg Pathol</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>23</volume><issue>8</issue><spage>638</spage><epage>648</epage><pages>638-648</pages><issn>1066-8969</issn><eissn>1940-2465</eissn><abstract>Introduction. Perivascular soft tissue tumors are relatively uncommon neoplasms of unclear line of differentiation, although most are presumed to originate from pericytes or modified perivascular cells. Among these, glomus tumor, myopericytoma, and angioleiomyoma share a spectrum of histologic findings and a perivascular growth pattern. In contrast, solitary fibrous tumor (previously termed hemangiopericytoma) was once hypothesized to have pericytic differentiation. Methods. Here, we systematically examine pericyte immunohistochemical markers among glomus tumor (including malignant glomus tumor), myopericytoma, angioleiomyoma, and solitary fibrous tumor. Immunohistochemical staining and semiquantification was performed using well-defined pericyte antigens, including αSMA, CD146, and PDGFRβ. Results. Glomus tumor and myopericytoma demonstrate diffuse staining for all pericyte markers, including immunohistochemical reactivity for αSMA, CD146, and PDGFRβ. Malignant glomus tumors all showed some degree of pericyte marker immunoreactivity, although it was significantly reduced. Angioleiomyoma shared a similar αSMA + CD146 + PDGFRβ+ immunophenotype; however, this was predominantly seen in the areas of perivascular tumor growth. Solitary fibrous tumors showed patchy PDGFRβ immunoreactivity only. Discussion. In summary, pericyte marker expression is a ubiquitous finding in glomus tumor, myopericytoma, and angioleiomyoma. Malignant glomus tumor shows a comparative reduction in pericyte marker expression, which may represent partial loss of pericytic differentiation. Pericyte markers are essentially not seen in solitary fibrous tumor. The combination of αSMA, CD146, and PDGFRβ immunohistochemical stainings may be of utility for the evaluation of pericytic differentiation in soft tissue tumors.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>26085647</pmid><doi>10.1177/1066896915591272</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1066-8969
ispartof International journal of surgical pathology, 2015-12, Vol.23 (8), p.638-648
issn 1066-8969
1940-2465
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4641786
source SAGE:Jisc Collections:SAGE Journals Read and Publish 2023-2024:2025 extension (reading list)
subjects Antigens, Neoplasm - analysis
Antigens, Neoplasm - biosynthesis
Biomarkers, Tumor - analysis
Humans
Immunohistochemistry
Pericytes - metabolism
Pericytes - pathology
Retrospective Studies
Soft Tissue Neoplasms - metabolism
Soft Tissue Neoplasms - pathology
title Pericyte Antigens in Perivascular Soft Tissue Tumors
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T07%3A36%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pericyte%20Antigens%20in%20Perivascular%20Soft%20Tissue%20Tumors&rft.jtitle=International%20journal%20of%20surgical%20pathology&rft.au=Shen,%20Jia&rft.date=2015-12-01&rft.volume=23&rft.issue=8&rft.spage=638&rft.epage=648&rft.pages=638-648&rft.issn=1066-8969&rft.eissn=1940-2465&rft_id=info:doi/10.1177/1066896915591272&rft_dat=%3Cproquest_pubme%3E1732599992%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c500t-306263ace2f0ae6ebd317f58c96a399c564fb4533a7b709121bec06a67a203c93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1732599992&rft_id=info:pmid/26085647&rft_sage_id=10.1177_1066896915591272&rfr_iscdi=true