Pseudomyxoma peritonei peritonitis
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.
Authors
- Bankole Oyewole (ORCID: https://orcid.org/0000-0001-7933-0472)
- Pranathi Yannamani (ORCID: https://orcid.org/0009-0004-8279-7005)
- Lillian Chungu
- Rajesh Shetty
Institutions
- Wye Valley NHS Trust (GB)
Publication Details
- Journal
- BMJ Case Reports
- Published
- 2024-08-01
- DOI
- https://doi.org/10.1136/bcr-2024-260759
- Primary Topic
- Intraperitoneal and Appendiceal Malignancies
- Type
- article
- Field-Weighted Citation Impact
- 0.00