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Updated: Jul 6, 2026

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults

Published on: February 28, 2025

[Hereditary angioedema causing colocolic intussusception].

A Sanchez¹, A Ecochard, M Maestracci

¹Pédiatrie III, CHU Arnaud-de-Villeneuve, 371, avenue du Doyen-Gaston-Giraud, 34295 Montpellier, France. tony.jose@caramail.com

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie

|March 11, 2008

Summary

This summary is machine-generated.

Hereditary angioedema, a rare genetic disorder, can manifest as severe digestive issues like intestinal intussusception in children. This case highlights the importance of recognizing this rare complication and its management.

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Last Updated: Jul 6, 2026

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults

Published on: February 28, 2025

Area of Science:

Genetics
Immunology
Pediatrics

Background:

Hereditary angioedema (HAE) is a rare autosomal dominant disorder caused by C1 inhibitor deficiency.
HAE presents with recurrent swelling, often affecting the skin, airways, and gastrointestinal tract.
Digestive manifestations, particularly intestinal intussusception, are infrequently reported in pediatric HAE cases.

Observation:

A 15-year-old female with a history of hereditary angioedema presented with symptoms suggestive of intestinal intussusception.
The patient's clinical presentation included severe abdominal pain and vomiting, consistent with a gastrointestinal emergency.
Diagnostic evaluation confirmed intestinal intussusception in the context of known HAE.

Findings:

This case represents a rare occurrence of intestinal intussusception as a manifestation of hereditary angioedema in a pediatric patient.
Literature review indicates limited data on the association between HAE and pediatric intestinal intussusception.
Prompt diagnosis and management are crucial for favorable outcomes in such cases.

Implications:

Highlights the need for increased awareness among clinicians regarding the potential for gastrointestinal complications, including intussusception, in pediatric patients with HAE.
Emphasizes the importance of considering HAE in the differential diagnosis of unexplained abdominal emergencies in children.
Suggests a need for further research into the pathophysiology and optimal management strategies for gastrointestinal crises in pediatric HAE.