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Pseudomyxoma peritonei peritonitis.
- Source :
-
BMJ case reports [BMJ Case Rep] 2024 Aug 22; Vol. 17 (8). Date of Electronic Publication: 2024 Aug 22. - Publication Year :
- 2024
-
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.<br />Competing Interests: Competing interests: None declared.<br /> (© BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ.)
- Subjects :
- Humans
Male
Adult
Appendectomy
Laparoscopy
Abdominal Pain etiology
Appendiceal Neoplasms diagnosis
Appendiceal Neoplasms surgery
Appendiceal Neoplasms complications
Diagnosis, Differential
Pseudomyxoma Peritonei diagnosis
Pseudomyxoma Peritonei surgery
Pseudomyxoma Peritonei complications
Peritonitis diagnosis
Peritonitis surgery
Peritonitis etiology
Peritoneal Neoplasms diagnosis
Peritoneal Neoplasms surgery
Peritoneal Neoplasms complications
Tomography, X-Ray Computed
Subjects
Details
- Language :
- English
- ISSN :
- 1757-790X
- Volume :
- 17
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- BMJ case reports
- Publication Type :
- Academic Journal
- Accession number :
- 39179264
- Full Text :
- https://doi.org/10.1136/bcr-2024-260759