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Benign Multicystic Peritoneal Mesothelioma: A Rare Condition in an Uncommon Gender

Benign Multicystic Peritoneal Mesothelioma (BMPM) is a rare condition that arises from the abdominal peritoneum. Fewer than 200 cases have been reported worldwide. BMPM usually affects premenopausal women and is extremely rare in men. Many factors are suspected to contribute to its development, such...

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Autores principales: Khurram, Muhammad S., Shaikh, Hamadullah, Khan, Uqba, Edens, Jacob, Ibrar, Warda, Hamza, Ameer, Zaka, Awais, Bano, Roohi, Hadid, Tarik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451755/
https://www.ncbi.nlm.nih.gov/pubmed/28607791
http://dx.doi.org/10.1155/2017/9752908
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author Khurram, Muhammad S.
Shaikh, Hamadullah
Khan, Uqba
Edens, Jacob
Ibrar, Warda
Hamza, Ameer
Zaka, Awais
Bano, Roohi
Hadid, Tarik
author_facet Khurram, Muhammad S.
Shaikh, Hamadullah
Khan, Uqba
Edens, Jacob
Ibrar, Warda
Hamza, Ameer
Zaka, Awais
Bano, Roohi
Hadid, Tarik
author_sort Khurram, Muhammad S.
collection PubMed
description Benign Multicystic Peritoneal Mesothelioma (BMPM) is a rare condition that arises from the abdominal peritoneum. Fewer than 200 cases have been reported worldwide. BMPM usually affects premenopausal women and is extremely rare in men. Many factors are suspected to contribute to its development, such as previous surgery, endometriosis, and familial Mediterranean fever. The main management is surgical resection; however, it is estimated that the recurrence rate is up to 50%. Malignant transformation is rare. We report a case series of three male patients who were diagnosed with BMPM and were treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC).
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spelling pubmed-54517552017-06-12 Benign Multicystic Peritoneal Mesothelioma: A Rare Condition in an Uncommon Gender Khurram, Muhammad S. Shaikh, Hamadullah Khan, Uqba Edens, Jacob Ibrar, Warda Hamza, Ameer Zaka, Awais Bano, Roohi Hadid, Tarik Case Rep Pathol Case Report Benign Multicystic Peritoneal Mesothelioma (BMPM) is a rare condition that arises from the abdominal peritoneum. Fewer than 200 cases have been reported worldwide. BMPM usually affects premenopausal women and is extremely rare in men. Many factors are suspected to contribute to its development, such as previous surgery, endometriosis, and familial Mediterranean fever. The main management is surgical resection; however, it is estimated that the recurrence rate is up to 50%. Malignant transformation is rare. We report a case series of three male patients who were diagnosed with BMPM and were treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC). Hindawi 2017 2017-05-18 /pmc/articles/PMC5451755/ /pubmed/28607791 http://dx.doi.org/10.1155/2017/9752908 Text en Copyright © 2017 Muhammad S. Khurram et al. https://creativecommons.org/licenses/by/4.0/ 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
Khurram, Muhammad S.
Shaikh, Hamadullah
Khan, Uqba
Edens, Jacob
Ibrar, Warda
Hamza, Ameer
Zaka, Awais
Bano, Roohi
Hadid, Tarik
Benign Multicystic Peritoneal Mesothelioma: A Rare Condition in an Uncommon Gender
title Benign Multicystic Peritoneal Mesothelioma: A Rare Condition in an Uncommon Gender
title_full Benign Multicystic Peritoneal Mesothelioma: A Rare Condition in an Uncommon Gender
title_fullStr Benign Multicystic Peritoneal Mesothelioma: A Rare Condition in an Uncommon Gender
title_full_unstemmed Benign Multicystic Peritoneal Mesothelioma: A Rare Condition in an Uncommon Gender
title_short Benign Multicystic Peritoneal Mesothelioma: A Rare Condition in an Uncommon Gender
title_sort benign multicystic peritoneal mesothelioma: a rare condition in an uncommon gender
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451755/
https://www.ncbi.nlm.nih.gov/pubmed/28607791
http://dx.doi.org/10.1155/2017/9752908
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