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Immunohistochemical profiling of cytokeratin expression by endometrial stroma sarcoma

Summary Endometrial stromal sarcomas can be confused with several neoplasms because of their inconsistent and widely varied morphologic appearance and frequent immunohistochemical expression of a variety of antigens including cytokeratin. The resulting diagnostic challenge becomes problematic partic...

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Published in:Human pathology 2008-10, Vol.39 (10), p.1459-1464
Main Authors: Adegboyega, Patrick A., MD, Qiu, Suimin, MD, PhD
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description Summary Endometrial stromal sarcomas can be confused with several neoplasms because of their inconsistent and widely varied morphologic appearance and frequent immunohistochemical expression of a variety of antigens including cytokeratin. The resulting diagnostic challenge becomes problematic particularly in the diagnosis of metastases resulting from such tumors. Because of the sometime epithelioid appearance of the tumor cells and their expression of cytokeratin, the metastases may be misdiagnosed as poorly differentiated carcinoma. We therefore studied the profile of cytokeratin proteins expression in 17 cases of endometrial stromal sarcomas using a panel of antibodies including cytokeratin cocktail antibody (AE1/AE 3), CK5/6, CK7, CK14, CK16, Cam5.2 (CK8), CK19, CK20, and 34E β 12 (CK1, 5, 10, and 14). Of the 17 cases, 8 (47%) stained positive with the cytokeratin cocktail antibody (AE1/AE 3). Of the 8 cases with cytokeratin expression, 5 (63%) stained positive with CK19, and 3 of them stained positive with Cam5.2. The 3 cases that stained positive with Cam5.2 also expressed CK19. Of the 5 cases with CK19, 1 was focally positive for CK5/6, CK7, and 34E β 12. None of the cases expressed CK14, CK16, or CK20. These results show that CK19 is most commonly expressed cytokeratin in endometrial stromal tumors. Hence, the inclusion of CK19 in the panel of immunostains may help resolve the diagnostic confusion created by keratin expression in endometrial stromal sarcoma and may also help in the correct diagnosis of endometrial stromal sarcoma at extrauterine sites.
doi_str_mv 10.1016/j.humpath.2008.02.008
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The resulting diagnostic challenge becomes problematic particularly in the diagnosis of metastases resulting from such tumors. Because of the sometime epithelioid appearance of the tumor cells and their expression of cytokeratin, the metastases may be misdiagnosed as poorly differentiated carcinoma. We therefore studied the profile of cytokeratin proteins expression in 17 cases of endometrial stromal sarcomas using a panel of antibodies including cytokeratin cocktail antibody (AE1/AE 3), CK5/6, CK7, CK14, CK16, Cam5.2 (CK8), CK19, CK20, and 34E β 12 (CK1, 5, 10, and 14). Of the 17 cases, 8 (47%) stained positive with the cytokeratin cocktail antibody (AE1/AE 3). Of the 8 cases with cytokeratin expression, 5 (63%) stained positive with CK19, and 3 of them stained positive with Cam5.2. The 3 cases that stained positive with Cam5.2 also expressed CK19. Of the 5 cases with CK19, 1 was focally positive for CK5/6, CK7, and 34E β 12. None of the cases expressed CK14, CK16, or CK20. These results show that CK19 is most commonly expressed cytokeratin in endometrial stromal tumors. Hence, the inclusion of CK19 in the panel of immunostains may help resolve the diagnostic confusion created by keratin expression in endometrial stromal sarcoma and may also help in the correct diagnosis of endometrial stromal sarcoma at extrauterine sites.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2008.02.008</identifier><identifier>PMID: 18619644</identifier><identifier>CODEN: HPCQA4</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adenocarcinoma - diagnosis ; Biological and medical sciences ; Biomarkers, Tumor - metabolism ; Cancer ; Cytokeratin ; Diagnosis, Differential ; Endometrial ; Endometrial Neoplasms - metabolism ; Endometrial Neoplasms - pathology ; Female ; Humans ; Immunohistochemistry - methods ; Investigative techniques, diagnostic techniques (general aspects) ; Keratin-19 - metabolism ; Keratins - metabolism ; Medical sciences ; Neoplasm Metastasis - diagnosis ; Pathology ; Pathology. Cytology. Biochemistry. Spectrometry. 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The resulting diagnostic challenge becomes problematic particularly in the diagnosis of metastases resulting from such tumors. Because of the sometime epithelioid appearance of the tumor cells and their expression of cytokeratin, the metastases may be misdiagnosed as poorly differentiated carcinoma. We therefore studied the profile of cytokeratin proteins expression in 17 cases of endometrial stromal sarcomas using a panel of antibodies including cytokeratin cocktail antibody (AE1/AE 3), CK5/6, CK7, CK14, CK16, Cam5.2 (CK8), CK19, CK20, and 34E β 12 (CK1, 5, 10, and 14). Of the 17 cases, 8 (47%) stained positive with the cytokeratin cocktail antibody (AE1/AE 3). Of the 8 cases with cytokeratin expression, 5 (63%) stained positive with CK19, and 3 of them stained positive with Cam5.2. The 3 cases that stained positive with Cam5.2 also expressed CK19. Of the 5 cases with CK19, 1 was focally positive for CK5/6, CK7, and 34E β 12. None of the cases expressed CK14, CK16, or CK20. These results show that CK19 is most commonly expressed cytokeratin in endometrial stromal tumors. Hence, the inclusion of CK19 in the panel of immunostains may help resolve the diagnostic confusion created by keratin expression in endometrial stromal sarcoma and may also help in the correct diagnosis of endometrial stromal sarcoma at extrauterine sites.</description><subject>Adenocarcinoma - diagnosis</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cancer</subject><subject>Cytokeratin</subject><subject>Diagnosis, Differential</subject><subject>Endometrial</subject><subject>Endometrial Neoplasms - metabolism</subject><subject>Endometrial Neoplasms - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry - methods</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Keratin-19 - metabolism</subject><subject>Keratins - metabolism</subject><subject>Medical sciences</subject><subject>Neoplasm Metastasis - diagnosis</subject><subject>Pathology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Proteins</subject><subject>Sarcoma, Endometrial Stromal - metabolism</subject><subject>Sarcoma, Endometrial Stromal - secondary</subject><subject>Smooth muscle</subject><subject>Stromal Sarcoma</subject><subject>Tissue Array Analysis</subject><subject>Tumors</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkkFv1DAQhS0EokvhJ4AiIXpLasd27FyoUFVopUo9QCVuluNMWG-TeLETxP57JtqISr309A7zvdHMmyHkPaMFo6w63xXbedjbaVuUlOqClgXKC7Jhkpe55nX5kmwoFVWumVIn5E1KO0oZk0K-JidMV6yuhNiQ-5thmMew9WkKbguDd7bP9jF0vvfjryx0mTtM4QGinfyYwd99hJR8GLPmkMHYhgGm6NGSphgGmyUbHepb8qqzfYJ3q56S-69XPy6v89u7bzeXX25zJ1Q15UJ1mjvQ1rUKtGh0LUWjJHPQcqidw6ps2say0jlgTceB245yxCQthWX8lJwd--LEv2dIkxl8ctD3doQwJ1PVErevNIIfn4C7MMcRZzOMcqEVl_VCySPlYkgpQmf20Q82HhAyS-pmZ9bUzZK6oaVBQd-HtfvcDNA-utaYEfi0AjZhwF20o_PpP1fSSgnFFu7iyAGG9sdDNMl5GDEPH8FNpg3-2VE-P-ng8JDLVR_gAOlxa5PQYL4vL7J8CNX4HVT95P8Ag0G54w</recordid><startdate>20081001</startdate><enddate>20081001</enddate><creator>Adegboyega, Patrick A., MD</creator><creator>Qiu, Suimin, MD, PhD</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier Limited</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>20081001</creationdate><title>Immunohistochemical profiling of cytokeratin expression by endometrial stroma sarcoma</title><author>Adegboyega, Patrick A., MD ; Qiu, Suimin, MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-47f83ce8acd7e84b8954b751ced3e9ccf835bdba12cce1bf3e3af038955024a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adenocarcinoma - diagnosis</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cancer</topic><topic>Cytokeratin</topic><topic>Diagnosis, Differential</topic><topic>Endometrial</topic><topic>Endometrial Neoplasms - metabolism</topic><topic>Endometrial Neoplasms - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry - methods</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Keratin-19 - metabolism</topic><topic>Keratins - metabolism</topic><topic>Medical sciences</topic><topic>Neoplasm Metastasis - diagnosis</topic><topic>Pathology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Proteins</topic><topic>Sarcoma, Endometrial Stromal - metabolism</topic><topic>Sarcoma, Endometrial Stromal - secondary</topic><topic>Smooth muscle</topic><topic>Stromal Sarcoma</topic><topic>Tissue Array Analysis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Adegboyega, Patrick A., MD</creatorcontrib><creatorcontrib>Qiu, Suimin, MD, PhD</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>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Adegboyega, Patrick A., MD</au><au>Qiu, Suimin, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunohistochemical profiling of cytokeratin expression by endometrial stroma sarcoma</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>2008-10-01</date><risdate>2008</risdate><volume>39</volume><issue>10</issue><spage>1459</spage><epage>1464</epage><pages>1459-1464</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><coden>HPCQA4</coden><abstract>Summary Endometrial stromal sarcomas can be confused with several neoplasms because of their inconsistent and widely varied morphologic appearance and frequent immunohistochemical expression of a variety of antigens including cytokeratin. The resulting diagnostic challenge becomes problematic particularly in the diagnosis of metastases resulting from such tumors. Because of the sometime epithelioid appearance of the tumor cells and their expression of cytokeratin, the metastases may be misdiagnosed as poorly differentiated carcinoma. We therefore studied the profile of cytokeratin proteins expression in 17 cases of endometrial stromal sarcomas using a panel of antibodies including cytokeratin cocktail antibody (AE1/AE 3), CK5/6, CK7, CK14, CK16, Cam5.2 (CK8), CK19, CK20, and 34E β 12 (CK1, 5, 10, and 14). Of the 17 cases, 8 (47%) stained positive with the cytokeratin cocktail antibody (AE1/AE 3). Of the 8 cases with cytokeratin expression, 5 (63%) stained positive with CK19, and 3 of them stained positive with Cam5.2. The 3 cases that stained positive with Cam5.2 also expressed CK19. Of the 5 cases with CK19, 1 was focally positive for CK5/6, CK7, and 34E β 12. None of the cases expressed CK14, CK16, or CK20. These results show that CK19 is most commonly expressed cytokeratin in endometrial stromal tumors. Hence, the inclusion of CK19 in the panel of immunostains may help resolve the diagnostic confusion created by keratin expression in endometrial stromal sarcoma and may also help in the correct diagnosis of endometrial stromal sarcoma at extrauterine sites.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>18619644</pmid><doi>10.1016/j.humpath.2008.02.008</doi><tpages>6</tpages></addata></record>
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subjects Adenocarcinoma - diagnosis
Biological and medical sciences
Biomarkers, Tumor - metabolism
Cancer
Cytokeratin
Diagnosis, Differential
Endometrial
Endometrial Neoplasms - metabolism
Endometrial Neoplasms - pathology
Female
Humans
Immunohistochemistry - methods
Investigative techniques, diagnostic techniques (general aspects)
Keratin-19 - metabolism
Keratins - metabolism
Medical sciences
Neoplasm Metastasis - diagnosis
Pathology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Proteins
Sarcoma, Endometrial Stromal - metabolism
Sarcoma, Endometrial Stromal - secondary
Smooth muscle
Stromal Sarcoma
Tissue Array Analysis
Tumors
title Immunohistochemical profiling of cytokeratin expression by endometrial stroma sarcoma
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