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Case Reports
. 2024 Aug 22;17(8):e260759.
doi: 10.1136/bcr-2024-260759.

Pseudomyxoma peritonei peritonitis

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Case Reports

Pseudomyxoma peritonei peritonitis

Pranathi Yannamani et al. BMJ Case Rep. .

Abstract

Pseudomyxoma peritonei (PMP) is a rare neoplastic condition characterised by gelatinous ascites, which generally arise from mucin-producing appendiceal tumours. Presentation is variable but requires prompt recognition to ensure appropriate specialist management due to risk of malignancy.A male in his 40s presented with a 1-day history of sudden onset, non-migratory abdominal pain, worse in the right iliac fossa. He had no significant medical history nor known drug allergies. Examination revealed right iliac fossa peritonism and blood tests revealed raised inflammatory markers. CT scan showed a right-sided abdominal collection. Intraoperatively, a diagnostic laparoscopy was performed, which revealed extensive mucin in the abdominal cavity. This was washed out and a laparoscopic appendectomy was performed; histopathology confirmed PMP from the ruptured appendix.

Keywords: Gastrointestinal surgery; General surgery; Surgical oncology.

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Conflict of interest statement

Competing interests: None declared.

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