Benign multicystic peritoneal mesothelioma as a rare disease in an incidental imaging finding in a middle-aged woman: case report and literature review

Benign multicystic peritoneal mesothelioma (BMPM) is a rare, benign cystic neoplasm arising from the peritoneum, most frequently diagnosed in premenopausal women. Fewer than 200 cases have been reported worldwide. Risk factors include endometriosis and pelvic inflammatory disease in women, and prior abdominal surgery in both sexes. Due to its rarity and lack of specific clinical presentation, preoperative diagnosis is challenging, with most cases discovered incidentally. Diagnosis is confirmed through surgical sampling and histopathological analysis. Several treatment strategies have been proposed, with cytoreductive surgery being the standard approach. Long-term follow-up is essential due to the high recurrence rate and the rare possibility of malignant transformation.

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Publication Details

Journal
International Surgery Journal
Published
2026-10-27
DOI
https://doi.org/10.18203/2349-2902.isj20263863
Primary Topic
Intraperitoneal and Appendiceal Malignancies
Type
article
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article

Benign multicystic peritoneal mesothelioma as a rare disease in an incidental imaging finding in a middle-aged woman: case report and literature review

Patrícia Bárbara, Paulo Clara, Alexandra Rocha, Rita R. Banza et al.
2 links
International Surgery Journal
Intraperitoneal and Appendiceal Malignancies
article

Benign multicystic peritoneal mesothelioma as a rare disease in an incidental imaging finding in a middle-aged woman: case report and literature review

Patrícia Bárbara, Paulo Clara, Alexandra Rocha, Rita R. Banza, Sandra Amado, Maria Inês Coelho, Miguel C. Santos, João Nobre
article en

Abstract

Benign multicystic peritoneal mesothelioma (BMPM) is a rare, benign cystic neoplasm arising from the peritoneum, most frequently diagnosed in premenopausal women. Fewer than 200 cases have been reported worldwide. Risk factors include endometriosis and pelvic inflammatory disease in women, and prior abdominal surgery in both sexes. Due to its rarity and lack of specific clinical presentation, preoperative diagnosis is challenging, with most cases discovered incidentally. Diagnosis is confirmed through surgical sampling and histopathological analysis. Several treatment strategies have been proposed, with cytoreductive surgery being the standard approach. Long-term follow-up is essential due to the high recurrence rate and the rare possibility of malignant transformation.

International Surgery JournalVol. 13(11)
Unidade Local de Saúde da Região de Leiria (PT)
Good health and well-being
Openalex Percentile: Top 10%
Intraperitoneal and Appendiceal Malignancies
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