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A rare and distinct bilateral ovarian tumor: Carcinosarcoma
Carcinosarcomas are aggressive biphasic neoplasms composed of high‐grade, malignant, epithelial, and mesenchymal elements. They usually occur in the uterus and rarely involve the ovaries. Only 10% of them are bilateral. Their diagnosis relies on histological examination coupled with immunohistochemi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643488/ https://www.ncbi.nlm.nih.gov/pubmed/34917375 http://dx.doi.org/10.1002/ccr3.5160 |
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author | Limaiem, Faten Halouani, Ahmed Saffar, Khalil Bouraoui, Saâdia |
author_facet | Limaiem, Faten Halouani, Ahmed Saffar, Khalil Bouraoui, Saâdia |
author_sort | Limaiem, Faten |
collection | PubMed |
description | Carcinosarcomas are aggressive biphasic neoplasms composed of high‐grade, malignant, epithelial, and mesenchymal elements. They usually occur in the uterus and rarely involve the ovaries. Only 10% of them are bilateral. Their diagnosis relies on histological examination coupled with immunohistochemistry. |
format | Online Article Text |
id | pubmed-8643488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86434882021-12-15 A rare and distinct bilateral ovarian tumor: Carcinosarcoma Limaiem, Faten Halouani, Ahmed Saffar, Khalil Bouraoui, Saâdia Clin Case Rep Case Report Carcinosarcomas are aggressive biphasic neoplasms composed of high‐grade, malignant, epithelial, and mesenchymal elements. They usually occur in the uterus and rarely involve the ovaries. Only 10% of them are bilateral. Their diagnosis relies on histological examination coupled with immunohistochemistry. John Wiley and Sons Inc. 2021-12-04 /pmc/articles/PMC8643488/ /pubmed/34917375 http://dx.doi.org/10.1002/ccr3.5160 Text en © 2021 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Limaiem, Faten Halouani, Ahmed Saffar, Khalil Bouraoui, Saâdia A rare and distinct bilateral ovarian tumor: Carcinosarcoma |
title | A rare and distinct bilateral ovarian tumor: Carcinosarcoma |
title_full | A rare and distinct bilateral ovarian tumor: Carcinosarcoma |
title_fullStr | A rare and distinct bilateral ovarian tumor: Carcinosarcoma |
title_full_unstemmed | A rare and distinct bilateral ovarian tumor: Carcinosarcoma |
title_short | A rare and distinct bilateral ovarian tumor: Carcinosarcoma |
title_sort | rare and distinct bilateral ovarian tumor: carcinosarcoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643488/ https://www.ncbi.nlm.nih.gov/pubmed/34917375 http://dx.doi.org/10.1002/ccr3.5160 |
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