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Benign Multicystic Peritoneal Mesothelioma: A Rare Condition in an Uncommon Gender
Muhammad S Khurram1, Hamadullah Shaikh2, Uqba Khan1
1St. John Hospital and Medical Center, Detroit, MI 48236, USA.
Abstract:
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).
Insights
Benign Multicystic Peritoneal Mesothelioma (BMPM) is rare, typically affecting women. This study presents three male cases treated successfully with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC).
Area of Science:
- Oncology
- Gastroenterology
- Surgical Pathology
Background:
- Benign Multicystic Peritoneal Mesothelioma (BMPM) is a rare neoplastic condition originating in the abdominal peritoneum.
- Fewer than 200 cases globally, predominantly affecting premenopausal women, with rarity in males.
- Potential contributing factors include prior surgery, endometriosis, and familial Mediterranean fever.
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