Loading…

Peritoneal encapsulation – An unusual cause of acute bowel obstruction: A case report

Peritoneal encapsulation (PE) is a rare congenital anomaly characterised by the presence of an accessory peritoneal membrane which encases part of the small bowel. Typically, this remains asymptomatic, however; in rare cases, a person may present with symptoms suggestive of a small bowel obstruction...

Full description

Saved in:
Bibliographic Details
Published in:International journal of surgery case reports 2024-05, Vol.118, p.109616, Article 109616
Main Authors: Mahmood, Sarah, Srinivasan, Rajkumar, Berney, Christophe
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Peritoneal encapsulation (PE) is a rare congenital anomaly characterised by the presence of an accessory peritoneal membrane which encases part of the small bowel. Typically, this remains asymptomatic, however; in rare cases, a person may present with symptoms suggestive of a small bowel obstruction. Here we present a case of a 58 year old gentleman with congenital PE causing a bowel obstruction which was revealed on commuted tomography scan. He required a laparotomy and excision of the accessory sac. Pre-operative diagnosis of PE can be challenging. It can present as a bowel obstruction with unique features including asymmetric distension of the abdomen on clinical exam and cocoon-like cluster of small bowel on imaging. Congenital PE is a rare cause of bowel obstruction and should be considered early in patients presenting with symptoms of bowel obstruction without previous abdominal surgery. •Peritoneal encapsulation can present as a rare cause of small bowel obstruction•Unique features include asymmetric distension of the abdomen on examination and cocoon-like cluster of bowel on CT imaging•PE should be suspected as a cause of bowel obstructions in a virgin abdomen as it requires surgical management
ISSN:2210-2612
2210-2612
DOI:10.1016/j.ijscr.2024.109616