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Primary malignant mixed mullerian tumor of the peritoneum: a case report

Malignant mixed mullerian tumor (MMMT) occurs rarely extragenital sites and generally originates from female genital tracts such as the uterus. Here, we report a patient with a primary MMMT of the peritoneum in a 64-year-old woman, who experienced a discontinuous epigastric pain and an abdominal dis...

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Detalles Bibliográficos
Autores principales: Chen, Haidi, Hu, Peipei, Wu, Fusheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797966/
https://www.ncbi.nlm.nih.gov/pubmed/35116839
http://dx.doi.org/10.21037/tcr.2019.05.07
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author Chen, Haidi
Hu, Peipei
Wu, Fusheng
author_facet Chen, Haidi
Hu, Peipei
Wu, Fusheng
author_sort Chen, Haidi
collection PubMed
description Malignant mixed mullerian tumor (MMMT) occurs rarely extragenital sites and generally originates from female genital tracts such as the uterus. Here, we report a patient with a primary MMMT of the peritoneum in a 64-year-old woman, who experienced a discontinuous epigastric pain and an abdominal distention for 3 months. An ultrasound-guided fine needle aspiration biopsy (FNA) was executed and indicated a highly malignant soft tissue sarcoma. And after that, the patient received a tumor resection (cytoreductive surgery) and postoperative chemotherapy. The postoperative immunohistochemical analysis revealed a MMMT in peritoneum. Up to now, the patient has survived for 5 months.
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spelling pubmed-87979662022-02-02 Primary malignant mixed mullerian tumor of the peritoneum: a case report Chen, Haidi Hu, Peipei Wu, Fusheng Transl Cancer Res Case Report Malignant mixed mullerian tumor (MMMT) occurs rarely extragenital sites and generally originates from female genital tracts such as the uterus. Here, we report a patient with a primary MMMT of the peritoneum in a 64-year-old woman, who experienced a discontinuous epigastric pain and an abdominal distention for 3 months. An ultrasound-guided fine needle aspiration biopsy (FNA) was executed and indicated a highly malignant soft tissue sarcoma. And after that, the patient received a tumor resection (cytoreductive surgery) and postoperative chemotherapy. The postoperative immunohistochemical analysis revealed a MMMT in peritoneum. Up to now, the patient has survived for 5 months. AME Publishing Company 2019-06 /pmc/articles/PMC8797966/ /pubmed/35116839 http://dx.doi.org/10.21037/tcr.2019.05.07 Text en 2019 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Case Report
Chen, Haidi
Hu, Peipei
Wu, Fusheng
Primary malignant mixed mullerian tumor of the peritoneum: a case report
title Primary malignant mixed mullerian tumor of the peritoneum: a case report
title_full Primary malignant mixed mullerian tumor of the peritoneum: a case report
title_fullStr Primary malignant mixed mullerian tumor of the peritoneum: a case report
title_full_unstemmed Primary malignant mixed mullerian tumor of the peritoneum: a case report
title_short Primary malignant mixed mullerian tumor of the peritoneum: a case report
title_sort primary malignant mixed mullerian tumor of the peritoneum: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797966/
https://www.ncbi.nlm.nih.gov/pubmed/35116839
http://dx.doi.org/10.21037/tcr.2019.05.07
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