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Inhibin and CD99 (MIC2) expression in uterine stromal neoplasms with sex-cord-like elements

Uterine mesenchymal neoplasms with sex-cord-like elements are designated as endometrial stromal tumor with sex-cord-like elements (ESTSCLE) or uterine tumor resembling ovarian sex-cord tumor (UTROSCT), depending on the extent of sex-cord-like differentiation. Occasionally, sex-cord elements similar...

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Published in:Human pathology 1999-06, Vol.30 (6), p.671-679
Main Authors: Baker, Robin J, Hildebrandt, Richard H, Rouse, Robert V, Hendrickson, Michael R, Longacre, Teri A
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description Uterine mesenchymal neoplasms with sex-cord-like elements are designated as endometrial stromal tumor with sex-cord-like elements (ESTSCLE) or uterine tumor resembling ovarian sex-cord tumor (UTROSCT), depending on the extent of sex-cord-like differentiation. Occasionally, sex-cord elements similar to those in ESTSCLE and UTROSCT occur in uterine adenosarcomas. To determine whether the sex-cord-like elements in these tumors show immunohistological evidence of sex-cord differentiation, we studied a series of uterine neoplasms for expression of inhibin, a peptide hormone expressed by normal ovarian granulosa cells and ovarian sex-cord neoplasms, and CD99, a protein also expressed by granulosa cells, Sertoli cells, and some ovarian sex-cord tumors. Thirty uterine mesenchymal neoplasms (five epithelioid or plexiform smooth muscle tumors, three endometrial stromal tumors, two mixed endometrial stromal and smooth muscle tumors, 10 ESTSCLE, five UTROSCT, and five miscellaneous stromal processes) and five epithelial neoplasms were evaluated for expression of CD99 (clone 12E7) and inhibin (clone R1) in formalin-fixed, paraffin-embedded tissue. Three of 10 (30%) ESTSCLE and five of five (100%) UTROSCT were inhibin and CD99 immunoreactive. Inhibin staining was confined to the areas with sex-cord-like differentation, and staining was generally much stronger and more extensive in areas featuring prominent foam cells. There were no differences in the degree or intensity of staining for inhibin in premenopausal and postmenopausal women. CD99 expression tended to correlate with inhibin and was typically confined to similar cell types in the individual neoplasms. Weak CD99 immunoreactivity was seen in one additional epithelioid smooth muscle tumor, whereas all other mesenchymal and epithelial neoplasms studied for inhibin and CD99 were negative. These results provide further immunohistological support for true sex-cord differentiation within uterine mesenchymal proliferations and suggest that the degree of sex-cord differentiation may correlate with the expression of these markers.
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Andrology. Obstetrics</topic><topic>Humans</topic><topic>inhibin</topic><topic>Inhibins - biosynthesis</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Sex Cord-Gonadal Stromal Tumors - metabolism</topic><topic>sex-cord-like elements</topic><topic>Tumors</topic><topic>Uterine Neoplasms - metabolism</topic><topic>uterine stromal neoplasms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baker, Robin J</creatorcontrib><creatorcontrib>Hildebrandt, Richard H</creatorcontrib><creatorcontrib>Rouse, Robert V</creatorcontrib><creatorcontrib>Hendrickson, Michael R</creatorcontrib><creatorcontrib>Longacre, Teri A</creatorcontrib><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>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baker, Robin J</au><au>Hildebrandt, Richard H</au><au>Rouse, Robert V</au><au>Hendrickson, Michael R</au><au>Longacre, Teri A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibin and CD99 (MIC2) expression in uterine stromal neoplasms with sex-cord-like elements</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>1999-06-01</date><risdate>1999</risdate><volume>30</volume><issue>6</issue><spage>671</spage><epage>679</epage><pages>671-679</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><coden>HPCQA4</coden><abstract>Uterine mesenchymal neoplasms with sex-cord-like elements are designated as endometrial stromal tumor with sex-cord-like elements (ESTSCLE) or uterine tumor resembling ovarian sex-cord tumor (UTROSCT), depending on the extent of sex-cord-like differentiation. Occasionally, sex-cord elements similar to those in ESTSCLE and UTROSCT occur in uterine adenosarcomas. To determine whether the sex-cord-like elements in these tumors show immunohistological evidence of sex-cord differentiation, we studied a series of uterine neoplasms for expression of inhibin, a peptide hormone expressed by normal ovarian granulosa cells and ovarian sex-cord neoplasms, and CD99, a protein also expressed by granulosa cells, Sertoli cells, and some ovarian sex-cord tumors. Thirty uterine mesenchymal neoplasms (five epithelioid or plexiform smooth muscle tumors, three endometrial stromal tumors, two mixed endometrial stromal and smooth muscle tumors, 10 ESTSCLE, five UTROSCT, and five miscellaneous stromal processes) and five epithelial neoplasms were evaluated for expression of CD99 (clone 12E7) and inhibin (clone R1) in formalin-fixed, paraffin-embedded tissue. Three of 10 (30%) ESTSCLE and five of five (100%) UTROSCT were inhibin and CD99 immunoreactive. Inhibin staining was confined to the areas with sex-cord-like differentation, and staining was generally much stronger and more extensive in areas featuring prominent foam cells. There were no differences in the degree or intensity of staining for inhibin in premenopausal and postmenopausal women. CD99 expression tended to correlate with inhibin and was typically confined to similar cell types in the individual neoplasms. Weak CD99 immunoreactivity was seen in one additional epithelioid smooth muscle tumor, whereas all other mesenchymal and epithelial neoplasms studied for inhibin and CD99 were negative. 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subjects 12E7 Antigen
Adult
Aged
Antigens, CD - biosynthesis
Biological and medical sciences
CD99
Cell Adhesion Molecules - biosynthesis
Female
Female genital diseases
Gynecology. Andrology. Obstetrics
Humans
inhibin
Inhibins - biosynthesis
Medical sciences
Middle Aged
Sex Cord-Gonadal Stromal Tumors - metabolism
sex-cord-like elements
Tumors
Uterine Neoplasms - metabolism
uterine stromal neoplasms
title Inhibin and CD99 (MIC2) expression in uterine stromal neoplasms with sex-cord-like elements
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