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Endometrial stromal sarcomas : Immunohistochemical, electron microscopical and cytogenetic findings in two cases
Uterine sarcomas are approximately 3% of all malignant uterine corpus tumours. Of these, the tumours that originate solely in the stromal elements of the uterine wall are infrequent and have not been well characterized cytogenetically. We report two cases of endometrial stromal sarcomas (ESS), one l...
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Published in: | Virchows Archiv : an international journal of pathology 1999-04, Vol.434 (4), p.307-314 |
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container_title | Virchows Archiv : an international journal of pathology |
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creator | GIL-BENSO, R LOPEZ-GINES, C NAVARRO, S CARDA, C LLOMBART-BOSCH, A |
description | Uterine sarcomas are approximately 3% of all malignant uterine corpus tumours. Of these, the tumours that originate solely in the stromal elements of the uterine wall are infrequent and have not been well characterized cytogenetically. We report two cases of endometrial stromal sarcomas (ESS), one low grade and one high grade, diagnosed by conventional histology, immunocytochemistry, electron microscopy and cytogenetics. Morphologically clear-cut differential structures were seen at optical, immunohistochemical, and electron microscopic levels, permitting a clear differential diagnosis. The low-grade ESS expressed hormonal receptors and vimentin, whereas the high-grade ESS showed no hormone receptors, high Ki-67 activity, and occasional cytokeratin-positive cells. Ultrastructurally, no malignant epithelial differentiation was seen in the tumour cells, but cilia were found in both cases. Cytogenetic study of the low-grade ESS showed pseudodiploid karyotype with chromosomes 6 and 20 rearranged. The high-grade ESS showed a complex karyotype with clonal numerical and structural anomalies. The chromosomes involved in the structural rearrangements were 1, 3, 6, 7, 13, 14, 15, 17, 19, and 21. |
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Obstetrics ; Humans ; Immunoenzyme Techniques ; Karyotyping ; Medical sciences ; Microscopy, Electron ; Middle Aged ; Sarcoma, Endometrial Stromal - chemistry ; Sarcoma, Endometrial Stromal - genetics ; Sarcoma, Endometrial Stromal - pathology ; Sarcoma, Endometrial Stromal - therapy ; Tumors</subject><ispartof>Virchows Archiv : an international journal of pathology, 1999-04, Vol.434 (4), p.307-314</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c318t-2be622c3ed85e9de9189c27c8a0d0ea8b7a9bc68edc5f40a73849c275138541b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1773570$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10335941$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GIL-BENSO, R</creatorcontrib><creatorcontrib>LOPEZ-GINES, C</creatorcontrib><creatorcontrib>NAVARRO, S</creatorcontrib><creatorcontrib>CARDA, C</creatorcontrib><creatorcontrib>LLOMBART-BOSCH, A</creatorcontrib><title>Endometrial stromal sarcomas : Immunohistochemical, electron microscopical and cytogenetic findings in two cases</title><title>Virchows Archiv : an international journal of pathology</title><addtitle>Virchows Arch</addtitle><description>Uterine sarcomas are approximately 3% of all malignant uterine corpus tumours. Of these, the tumours that originate solely in the stromal elements of the uterine wall are infrequent and have not been well characterized cytogenetically. We report two cases of endometrial stromal sarcomas (ESS), one low grade and one high grade, diagnosed by conventional histology, immunocytochemistry, electron microscopy and cytogenetics. Morphologically clear-cut differential structures were seen at optical, immunohistochemical, and electron microscopic levels, permitting a clear differential diagnosis. The low-grade ESS expressed hormonal receptors and vimentin, whereas the high-grade ESS showed no hormone receptors, high Ki-67 activity, and occasional cytokeratin-positive cells. Ultrastructurally, no malignant epithelial differentiation was seen in the tumour cells, but cilia were found in both cases. Cytogenetic study of the low-grade ESS showed pseudodiploid karyotype with chromosomes 6 and 20 rearranged. The high-grade ESS showed a complex karyotype with clonal numerical and structural anomalies. The chromosomes involved in the structural rearrangements were 1, 3, 6, 7, 13, 14, 15, 17, 19, and 21.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Chromosome Aberrations - genetics</subject><subject>Chromosome Banding</subject><subject>Chromosome Disorders</subject><subject>Chromosomes, Human, Pair 20 - genetics</subject><subject>Chromosomes, Human, Pair 6 - genetics</subject><subject>Combined Modality Therapy</subject><subject>Endometrial Neoplasms - chemistry</subject><subject>Endometrial Neoplasms - genetics</subject><subject>Endometrial Neoplasms - pathology</subject><subject>Endometrial Neoplasms - therapy</subject><subject>Fatal Outcome</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Gynecology. Andrology. 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Andrology. Obstetrics</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Karyotyping</topic><topic>Medical sciences</topic><topic>Microscopy, Electron</topic><topic>Middle Aged</topic><topic>Sarcoma, Endometrial Stromal - chemistry</topic><topic>Sarcoma, Endometrial Stromal - genetics</topic><topic>Sarcoma, Endometrial Stromal - pathology</topic><topic>Sarcoma, Endometrial Stromal - therapy</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GIL-BENSO, R</creatorcontrib><creatorcontrib>LOPEZ-GINES, C</creatorcontrib><creatorcontrib>NAVARRO, S</creatorcontrib><creatorcontrib>CARDA, C</creatorcontrib><creatorcontrib>LLOMBART-BOSCH, 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>Virchows Archiv : an international journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GIL-BENSO, R</au><au>LOPEZ-GINES, C</au><au>NAVARRO, S</au><au>CARDA, C</au><au>LLOMBART-BOSCH, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endometrial stromal sarcomas : Immunohistochemical, electron microscopical and cytogenetic findings in two cases</atitle><jtitle>Virchows Archiv : an international journal of pathology</jtitle><addtitle>Virchows Arch</addtitle><date>1999-04-01</date><risdate>1999</risdate><volume>434</volume><issue>4</issue><spage>307</spage><epage>314</epage><pages>307-314</pages><issn>0945-6317</issn><eissn>1432-2307</eissn><abstract>Uterine sarcomas are approximately 3% of all malignant uterine corpus tumours. Of these, the tumours that originate solely in the stromal elements of the uterine wall are infrequent and have not been well characterized cytogenetically. We report two cases of endometrial stromal sarcomas (ESS), one low grade and one high grade, diagnosed by conventional histology, immunocytochemistry, electron microscopy and cytogenetics. Morphologically clear-cut differential structures were seen at optical, immunohistochemical, and electron microscopic levels, permitting a clear differential diagnosis. The low-grade ESS expressed hormonal receptors and vimentin, whereas the high-grade ESS showed no hormone receptors, high Ki-67 activity, and occasional cytokeratin-positive cells. Ultrastructurally, no malignant epithelial differentiation was seen in the tumour cells, but cilia were found in both cases. Cytogenetic study of the low-grade ESS showed pseudodiploid karyotype with chromosomes 6 and 20 rearranged. The high-grade ESS showed a complex karyotype with clonal numerical and structural anomalies. The chromosomes involved in the structural rearrangements were 1, 3, 6, 7, 13, 14, 15, 17, 19, and 21.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>10335941</pmid><doi>10.1007/s004280050346</doi><tpages>8</tpages></addata></record> |
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subjects | Aged Biological and medical sciences Biomarkers, Tumor - analysis Chromosome Aberrations - genetics Chromosome Banding Chromosome Disorders Chromosomes, Human, Pair 20 - genetics Chromosomes, Human, Pair 6 - genetics Combined Modality Therapy Endometrial Neoplasms - chemistry Endometrial Neoplasms - genetics Endometrial Neoplasms - pathology Endometrial Neoplasms - therapy Fatal Outcome Female Female genital diseases Gynecology. Andrology. Obstetrics Humans Immunoenzyme Techniques Karyotyping Medical sciences Microscopy, Electron Middle Aged Sarcoma, Endometrial Stromal - chemistry Sarcoma, Endometrial Stromal - genetics Sarcoma, Endometrial Stromal - pathology Sarcoma, Endometrial Stromal - therapy Tumors |
title | Endometrial stromal sarcomas : Immunohistochemical, electron microscopical and cytogenetic findings in two cases |
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