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Primary Cervical Carcinosarcoma: Report of a Rare Case
Background Carcinosarcomas are malignant mixed Müllerian tumors (MMMT), containing both epithelial and mesenchymal components. Carcinosarcomas of the uterine cervix comprise an extremely rare histopathological entity, with less than 150 cases reported in the literature to date. Materials and Method...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Medical Publishers, Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345680/ https://www.ncbi.nlm.nih.gov/pubmed/35928548 http://dx.doi.org/10.1055/s-0042-1744152 |
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author | Tsatsaris, Georgios Fasoulakis, Zacharias Koutras, Antonios Ntounis, Thomas Samara, Athina A. Syllaios, Athanasios Diamantis, Alexandros Kouroupi, Maria Stamos, Charilaos Kontomanolis, Emmanuel N. |
author_facet | Tsatsaris, Georgios Fasoulakis, Zacharias Koutras, Antonios Ntounis, Thomas Samara, Athina A. Syllaios, Athanasios Diamantis, Alexandros Kouroupi, Maria Stamos, Charilaos Kontomanolis, Emmanuel N. |
author_sort | Tsatsaris, Georgios |
collection | PubMed |
description | Background Carcinosarcomas are malignant mixed Müllerian tumors (MMMT), containing both epithelial and mesenchymal components. Carcinosarcomas of the uterine cervix comprise an extremely rare histopathological entity, with less than 150 cases reported in the literature to date. Materials and Methods A 79-year-old postmenopausal female patient was referred to our gynecological department due to a pelvic mass and vaginal bleeding. A cervical curettage was performed and the histological report revealed a malignant neoplasm with high cellularity consisting of two components; the first was a chondrosarcoma and the latter a adenocarcinoma. A diagnosis of MMMT was confirmed through immunohistochemical (IHC) staining. Neoadjuvant chemotherapy and radiotherapy were implemented, and a year later the patient underwent a radical hysterectomy and oncological pelvic lymph node dissection. She remains disease-free 12 months postoperatively. Conclusion Primary cervical carcinosarcomas are extremely rare tumors demonstrating a bipartite profile. Preoperative diagnosis with appropriate immunochemistry testing of this rare entity is crucial to decision making. |
format | Online Article Text |
id | pubmed-9345680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Thieme Medical Publishers, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93456802022-08-03 Primary Cervical Carcinosarcoma: Report of a Rare Case Tsatsaris, Georgios Fasoulakis, Zacharias Koutras, Antonios Ntounis, Thomas Samara, Athina A. Syllaios, Athanasios Diamantis, Alexandros Kouroupi, Maria Stamos, Charilaos Kontomanolis, Emmanuel N. Surg J (N Y) Background Carcinosarcomas are malignant mixed Müllerian tumors (MMMT), containing both epithelial and mesenchymal components. Carcinosarcomas of the uterine cervix comprise an extremely rare histopathological entity, with less than 150 cases reported in the literature to date. Materials and Methods A 79-year-old postmenopausal female patient was referred to our gynecological department due to a pelvic mass and vaginal bleeding. A cervical curettage was performed and the histological report revealed a malignant neoplasm with high cellularity consisting of two components; the first was a chondrosarcoma and the latter a adenocarcinoma. A diagnosis of MMMT was confirmed through immunohistochemical (IHC) staining. Neoadjuvant chemotherapy and radiotherapy were implemented, and a year later the patient underwent a radical hysterectomy and oncological pelvic lymph node dissection. She remains disease-free 12 months postoperatively. Conclusion Primary cervical carcinosarcomas are extremely rare tumors demonstrating a bipartite profile. Preoperative diagnosis with appropriate immunochemistry testing of this rare entity is crucial to decision making. Thieme Medical Publishers, Inc. 2022-08-02 /pmc/articles/PMC9345680/ /pubmed/35928548 http://dx.doi.org/10.1055/s-0042-1744152 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. ( https://creativecommons.org/licenses/by/4.0/ ) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Tsatsaris, Georgios Fasoulakis, Zacharias Koutras, Antonios Ntounis, Thomas Samara, Athina A. Syllaios, Athanasios Diamantis, Alexandros Kouroupi, Maria Stamos, Charilaos Kontomanolis, Emmanuel N. Primary Cervical Carcinosarcoma: Report of a Rare Case |
title | Primary Cervical Carcinosarcoma: Report of a Rare Case |
title_full | Primary Cervical Carcinosarcoma: Report of a Rare Case |
title_fullStr | Primary Cervical Carcinosarcoma: Report of a Rare Case |
title_full_unstemmed | Primary Cervical Carcinosarcoma: Report of a Rare Case |
title_short | Primary Cervical Carcinosarcoma: Report of a Rare Case |
title_sort | primary cervical carcinosarcoma: report of a rare case |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345680/ https://www.ncbi.nlm.nih.gov/pubmed/35928548 http://dx.doi.org/10.1055/s-0042-1744152 |
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