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Mass-like extragonadal endometriosis associated malignant transformation in the pelvis: A rare case report

BACKGROUND: Endometriosis affects approximately 10% of reproductive-age women, however, endometriosis associated malignant transformation is rare and is often report as a rare case. CASE SUMMARY: Herein, we report of a 49-year-old female patient who suffered from severe left lower abdominal pain and...

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Autores principales: Chen, Ping, Deng, Ya, Wang, Qiao-Qiao, Xu, Hong-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649542/
https://www.ncbi.nlm.nih.gov/pubmed/36387794
http://dx.doi.org/10.12998/wjcc.v10.i31.11567
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author Chen, Ping
Deng, Ya
Wang, Qiao-Qiao
Xu, Hong-Wei
author_facet Chen, Ping
Deng, Ya
Wang, Qiao-Qiao
Xu, Hong-Wei
author_sort Chen, Ping
collection PubMed
description BACKGROUND: Endometriosis affects approximately 10% of reproductive-age women, however, endometriosis associated malignant transformation is rare and is often report as a rare case. CASE SUMMARY: Herein, we report of a 49-year-old female patient who suffered from severe left lower abdominal pain and imaging examination revealed an irregular mass in the left iliac fossa. Histopathological examination revealed main undifferentiated adenocarcinoma with a few typical endometrial epithelial and stromal tissues in the adjacent area. Combined with the immunohistochemical staining and the negative intra- or postoperative results from exploratory laparotomy, gastroscopy, enteroscopy and positron emission tomography, the tumor was considered to be derived from endometriosis. The patient underwent hysterectomy, bilateral salpingectomy, bilateral ovariectomy, and multipoint biopsy of the pelvic peritoneum. Subsequent radiotherapy and chemotherapy were performed. The patient recovered well post-operation and there was no evidence of recurrence after 10 mo of follow-up via computed tomography and magnetic resonance imaging. CONCLUSION: This case highlights a rare presentation of mass-like extragonadal endometriosis associated malignant transformation in the pelvis. Endometriosis associated malignant transformation is rare and difficult to diagnose in clinical settings, with diagnoses depending on pathological results and the exclusion of metastasis from other organs. Fortunately, patients are often diagnosed at younger ages, as well as at early stages; thus they generally have relatively favorable prognoses.
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spelling pubmed-96495422022-11-15 Mass-like extragonadal endometriosis associated malignant transformation in the pelvis: A rare case report Chen, Ping Deng, Ya Wang, Qiao-Qiao Xu, Hong-Wei World J Clin Cases Case Report BACKGROUND: Endometriosis affects approximately 10% of reproductive-age women, however, endometriosis associated malignant transformation is rare and is often report as a rare case. CASE SUMMARY: Herein, we report of a 49-year-old female patient who suffered from severe left lower abdominal pain and imaging examination revealed an irregular mass in the left iliac fossa. Histopathological examination revealed main undifferentiated adenocarcinoma with a few typical endometrial epithelial and stromal tissues in the adjacent area. Combined with the immunohistochemical staining and the negative intra- or postoperative results from exploratory laparotomy, gastroscopy, enteroscopy and positron emission tomography, the tumor was considered to be derived from endometriosis. The patient underwent hysterectomy, bilateral salpingectomy, bilateral ovariectomy, and multipoint biopsy of the pelvic peritoneum. Subsequent radiotherapy and chemotherapy were performed. The patient recovered well post-operation and there was no evidence of recurrence after 10 mo of follow-up via computed tomography and magnetic resonance imaging. CONCLUSION: This case highlights a rare presentation of mass-like extragonadal endometriosis associated malignant transformation in the pelvis. Endometriosis associated malignant transformation is rare and difficult to diagnose in clinical settings, with diagnoses depending on pathological results and the exclusion of metastasis from other organs. Fortunately, patients are often diagnosed at younger ages, as well as at early stages; thus they generally have relatively favorable prognoses. Baishideng Publishing Group Inc 2022-11-06 2022-11-06 /pmc/articles/PMC9649542/ /pubmed/36387794 http://dx.doi.org/10.12998/wjcc.v10.i31.11567 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Report
Chen, Ping
Deng, Ya
Wang, Qiao-Qiao
Xu, Hong-Wei
Mass-like extragonadal endometriosis associated malignant transformation in the pelvis: A rare case report
title Mass-like extragonadal endometriosis associated malignant transformation in the pelvis: A rare case report
title_full Mass-like extragonadal endometriosis associated malignant transformation in the pelvis: A rare case report
title_fullStr Mass-like extragonadal endometriosis associated malignant transformation in the pelvis: A rare case report
title_full_unstemmed Mass-like extragonadal endometriosis associated malignant transformation in the pelvis: A rare case report
title_short Mass-like extragonadal endometriosis associated malignant transformation in the pelvis: A rare case report
title_sort mass-like extragonadal endometriosis associated malignant transformation in the pelvis: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649542/
https://www.ncbi.nlm.nih.gov/pubmed/36387794
http://dx.doi.org/10.12998/wjcc.v10.i31.11567
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