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Lipome géant pelvien mimant un liposarcome

Giant lipoma (GL) is a rare ubiquitous tumor. Pelvic lipoma is rare with less than 10 cases reported in the literature. The main differential diagnosis is lipoma-like well differentiated liposarcoma. We report the case of a 50-year old female patient, with a 3-month history of pelvic discomfort, pre...

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Autores principales: Dhouha, Bacha, Maroua, Walha, Seifeddine, Baccouch, Ghofrane, Talbi, Lassaad, Gharbi, Rached, Bayar, Rgaya, Mzabi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615766/
https://www.ncbi.nlm.nih.gov/pubmed/31312336
http://dx.doi.org/10.11604/pamj.2019.33.20.15008
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author Dhouha, Bacha
Maroua, Walha
Seifeddine, Baccouch
Ghofrane, Talbi
Lassaad, Gharbi
Rached, Bayar
Rgaya, Mzabi
author_facet Dhouha, Bacha
Maroua, Walha
Seifeddine, Baccouch
Ghofrane, Talbi
Lassaad, Gharbi
Rached, Bayar
Rgaya, Mzabi
author_sort Dhouha, Bacha
collection PubMed
description Giant lipoma (GL) is a rare ubiquitous tumor. Pelvic lipoma is rare with less than 10 cases reported in the literature. The main differential diagnosis is lipoma-like well differentiated liposarcoma. We report the case of a 50-year old female patient, with a 3-month history of pelvic discomfort, presenting with a mass in the left ischiorectal fossa. Abdominopelvic CT scan showed presacral hypodense homogeneous lipomatous mass measuring 10x18 cm. MRI showed hyperintense lesion on T1 and T2 -weighted images with fine partition walls reaching the 2(nd) sacral vertebra. Total abdominoperineal resection was performed without rupture of tumor capsule. Anatomo-pathological examination confirmed the diagnosis of GL. This study aims to report a new case of giant presacral pelvic lipoma which extends into the left ischiorectal fossa.
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spelling pubmed-66157662019-07-16 Lipome géant pelvien mimant un liposarcome Dhouha, Bacha Maroua, Walha Seifeddine, Baccouch Ghofrane, Talbi Lassaad, Gharbi Rached, Bayar Rgaya, Mzabi Pan Afr Med J Case Report Giant lipoma (GL) is a rare ubiquitous tumor. Pelvic lipoma is rare with less than 10 cases reported in the literature. The main differential diagnosis is lipoma-like well differentiated liposarcoma. We report the case of a 50-year old female patient, with a 3-month history of pelvic discomfort, presenting with a mass in the left ischiorectal fossa. Abdominopelvic CT scan showed presacral hypodense homogeneous lipomatous mass measuring 10x18 cm. MRI showed hyperintense lesion on T1 and T2 -weighted images with fine partition walls reaching the 2(nd) sacral vertebra. Total abdominoperineal resection was performed without rupture of tumor capsule. Anatomo-pathological examination confirmed the diagnosis of GL. This study aims to report a new case of giant presacral pelvic lipoma which extends into the left ischiorectal fossa. The African Field Epidemiology Network 2019-05-14 /pmc/articles/PMC6615766/ /pubmed/31312336 http://dx.doi.org/10.11604/pamj.2019.33.20.15008 Text en © Bacha Dhouha et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. 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 Case Report
Dhouha, Bacha
Maroua, Walha
Seifeddine, Baccouch
Ghofrane, Talbi
Lassaad, Gharbi
Rached, Bayar
Rgaya, Mzabi
Lipome géant pelvien mimant un liposarcome
title Lipome géant pelvien mimant un liposarcome
title_full Lipome géant pelvien mimant un liposarcome
title_fullStr Lipome géant pelvien mimant un liposarcome
title_full_unstemmed Lipome géant pelvien mimant un liposarcome
title_short Lipome géant pelvien mimant un liposarcome
title_sort lipome géant pelvien mimant un liposarcome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615766/
https://www.ncbi.nlm.nih.gov/pubmed/31312336
http://dx.doi.org/10.11604/pamj.2019.33.20.15008
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