Delayed presentation of multiple congenital intestinal webs.
BMJ Case Rep 2026 Apr 24; 19(4).

Abstract

Congenital intestinal webs of the bowel are an exceedingly rare cause of mechanical bowel obstruction in adults. Their presentation beyond the neonatal period is rare and may represent a diagnostic challenge. We report a case of multiple intestinal webs in an adolescent patient who initially presented with chronic abdominal pain, constipation and iron deficiency anaemia refractory to oral supplementation. The patient underwent evaluation for multiple gastrointestinal pathologies, including coeliac disease, eosinophilic gastrointestinal disorders and inflammatory bowel disease. As part of the evaluation, the patient underwent wireless capsule endoscopy. However, the capsule failed to progress beyond the small bowel. Laparoscopic-assisted retrieval revealed 18 intestinal webs which were surgically resected with subsequent resolution of symptoms. Although rare, failure of progression of a wireless capsule endoscope should raise concerns of possible intestinal webs in children as an underlying aetiology. Intestinal strictures should be further investigated and multiple webs must always be ruled out.

Authors+Show Affiliations

El-Gohary Y0000-0002-8655-0948Division of Pediatric General, Thoracic and Fetal Surgery, Chidren's Hospital Univeristy of Missouri, Columbia, Missouri, USA yousef.gohary@health.missouri.edu.
Chung CDivision of Pediatric General, Thoracic and Fetal Surgery, Chidren's Hospital Univeristy of Missouri, Columbia, Missouri, USA.
Hammoud GMDivision of Gastroenterology and Hepatology, University of Missouri System, Columbia, Missouri, USA.
Chen CBDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, University of Missouri System, Columbia, Missouri, USA.
Severance TDivision of Pediatric Hematology Oncology, University of Missouri System, Columbia, Missouri, USA.
Marwan AIDivision of Pediatric General, Thoracic and Fetal Surgery, Chidren's Hospital Univeristy of Missouri, Columbia, Missouri, USA.

Pub Type(s)

Journal Article
Case Reports

Language

eng

PubMed ID

42031383