ArticleInternational journal of surgery case reports2025
A case report of a rare etiology of an abdominal cystic lesion in adults: Peritoneal inclusion cysts.
Article in International journal of surgery case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Peritoneal Inclusion Cyst in an Unusual Location in a "Virgin" Abdomen: A Diagnostic Dilemma Expanding the Clinical Spectrum.Annals of African medicine · 2026Article
- Clinical Outcomes of Retained Plastic Biliary Stents: A Targeted Narrative Review.Digestive diseases and sciences · 2026Review
- Peritoneal inclusion cyst presenting as a rectocele after sacrohysteropexy: A case report.Case reports in women's health · 2025Article
- A large peritoneal inclusion cyst in a postmenopausal female without risk factors.Radiology case reports · 2025Article
- Peritoneal Inclusion Cyst Mimicking Adrenal Pathology in a Young Man: A Rare Case Report.Case reports in endocrinology · 2025Article
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6 authors.
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Abstract
introduction and importancePeritoneal inclusion cysts (PICs), also known as peritoneal mesothelial cysts, are rare, benign cystic lesions primarily occurring in the abdominopelvic cavity of premenopausal women with histories of pelvic surgery or inflammation. These cysts can present with nonspecific symptoms and may mimic other abdominal pathologies, making diagnosis challenging. CASE PRESENTATION: A 41-year-old male with no significant medical history, who experienced progressive nonspecific abdominal pain over several months. Clinical examination revealed a poorly defined mass in the right hemi-abdomen. Imaging studies, including CT and MRI, identified an elongated subhepatic cystic lesion, suggesting a peritoneal inclusion cyst or mesenteric cyst. Surgical intervention was decided following multidisciplinary team consultation. Intraoperative findings revealed a 13 cm intraperitoneal cyst with clear fluid content in the right hemi-abdomen, adherent to adjacent structures. Monobloc cystectomy was performed, and a histopathological examination confirmed the diagnosis of a peritoneal inclusion cyst. CLINICAL DISCUSSION: PICs are rare and typically affect females, with only limited cases reported in males. These cysts can be asymptomatic or present with non-specific symptoms such as abdominal pain or distension, often requiring imaging and, occasionally, surgical exploration for diagnosis. The differential diagnosis includes other cystic abdominal lesions, emphasizing the need for thorough clinical and imaging assessment. The preferred management of PICs is surgical excision, as it provides histological confirmation and minimizes recurrence risk.
conclusionThis case highlights a rare presentation of a PIC in a male patient, underscoring the importance of considering PICs within the differential diagnosis of abdominal cystic lesions regardless of patient gender. Surgical resection remains the primary management approach, but further research is needed to establish standardized guidelines for diagnosis and treatment.
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