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Clear Cell Adenocarcinoma Arising from Abdominal Wall Endometriosis

Endometriosis is a frequent benign disorder. Malignancy arising in extraovarian endometriosis is a rare event. A 49-year-old woman is presented with a large painful abdominal wall mass. She underwent a myomectomy, 20 years before, for uterus leiomyoma. Computed tomography suggested that this was a d...

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Autores principales: Achach, Thouraya, Rammeh, Soumaya, Trabelsi, Amel, Ltaief, Rached, Ben Abdelkrim, Soumaya, Mokni, Moncef, Korbi, Sadok
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648644/
https://www.ncbi.nlm.nih.gov/pubmed/19266089
http://dx.doi.org/10.1155/2008/478325
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author Achach, Thouraya
Rammeh, Soumaya
Trabelsi, Amel
Ltaief, Rached
Ben Abdelkrim, Soumaya
Mokni, Moncef
Korbi, Sadok
author_facet Achach, Thouraya
Rammeh, Soumaya
Trabelsi, Amel
Ltaief, Rached
Ben Abdelkrim, Soumaya
Mokni, Moncef
Korbi, Sadok
author_sort Achach, Thouraya
collection PubMed
description Endometriosis is a frequent benign disorder. Malignancy arising in extraovarian endometriosis is a rare event. A 49-year-old woman is presented with a large painful abdominal wall mass. She underwent a myomectomy, 20 years before, for uterus leiomyoma. Computed tomography suggested that this was a desmoid tumor and she underwent surgery. Histological examination showed a clear cell adenocarcinoma associated with endometriosis foci. Pelvic ultrasound, computed tomography, and endometrial curettage did not show any malignancy or endometriosis in the uterus and ovaries. Adjuvant chemotherapy was recommended, but the patient was lost to follow up. Six months later, she returned with a recurrence of the abdominal wall mass. She was given chemotherapy and then she was reoperated.
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spelling pubmed-26486442009-03-05 Clear Cell Adenocarcinoma Arising from Abdominal Wall Endometriosis Achach, Thouraya Rammeh, Soumaya Trabelsi, Amel Ltaief, Rached Ben Abdelkrim, Soumaya Mokni, Moncef Korbi, Sadok J Oncol Case Report Endometriosis is a frequent benign disorder. Malignancy arising in extraovarian endometriosis is a rare event. A 49-year-old woman is presented with a large painful abdominal wall mass. She underwent a myomectomy, 20 years before, for uterus leiomyoma. Computed tomography suggested that this was a desmoid tumor and she underwent surgery. Histological examination showed a clear cell adenocarcinoma associated with endometriosis foci. Pelvic ultrasound, computed tomography, and endometrial curettage did not show any malignancy or endometriosis in the uterus and ovaries. Adjuvant chemotherapy was recommended, but the patient was lost to follow up. Six months later, she returned with a recurrence of the abdominal wall mass. She was given chemotherapy and then she was reoperated. Hindawi Publishing Corporation 2008 2008-12-21 /pmc/articles/PMC2648644/ /pubmed/19266089 http://dx.doi.org/10.1155/2008/478325 Text en Copyright © 2008 Thouraya Achach et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Achach, Thouraya
Rammeh, Soumaya
Trabelsi, Amel
Ltaief, Rached
Ben Abdelkrim, Soumaya
Mokni, Moncef
Korbi, Sadok
Clear Cell Adenocarcinoma Arising from Abdominal Wall Endometriosis
title Clear Cell Adenocarcinoma Arising from Abdominal Wall Endometriosis
title_full Clear Cell Adenocarcinoma Arising from Abdominal Wall Endometriosis
title_fullStr Clear Cell Adenocarcinoma Arising from Abdominal Wall Endometriosis
title_full_unstemmed Clear Cell Adenocarcinoma Arising from Abdominal Wall Endometriosis
title_short Clear Cell Adenocarcinoma Arising from Abdominal Wall Endometriosis
title_sort clear cell adenocarcinoma arising from abdominal wall endometriosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648644/
https://www.ncbi.nlm.nih.gov/pubmed/19266089
http://dx.doi.org/10.1155/2008/478325
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