Pseudomyxoma peritonei peritonitis.


Journal

BMJ case reports
ISSN: 1757-790X
Titre abrégé: BMJ Case Rep
Pays: England
ID NLM: 101526291

Informations de publication

Date de publication:
22 Aug 2024
Historique:
medline: 24 8 2024
pubmed: 24 8 2024
entrez: 23 8 2024
Statut: epublish

Résumé

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.

Identifiants

pubmed: 39179264
pii: 17/8/e260759
doi: 10.1136/bcr-2024-260759
pii:
doi:

Types de publication

Journal Article Case Reports

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Pranathi Yannamani (P)

Wye Valley NHS Trust, Hereford, Herefordshire, UK pranathiyannamani@gmail.com.

Lillian Chungu (L)

Wye Valley NHS Trust, Hereford, Herefordshire, UK.

Rajesh Shetty (R)

Wye Valley NHS Trust, Hereford, Herefordshire, UK.

Bankole Oyewole (B)

Wye Valley NHS Trust, Hereford, Herefordshire, UK.

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Classifications MeSH