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Published on: July 11, 2013
A rare complication of Meckel's diverticulum: a fistula between Meckel's diverticulum and the appendix
Ping-Fu Yang1, Chau-Yun Chen, Fang-Jung Yu
1Division of Gastroenterology and General Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Abstract:
Meckel diverticulum is the most common congenital anomaly of the small intestine, occurring in about 2%-4% of the population. Meckel diverticulum results from incomplete closure of the omphalomesenteric duct. The presentation of symptomatic Meckel diverticulum includes gastrointestinal hemorrhage, intestinal obstruction, volvulus, intussusception, diverticulitis, and neoplasms. The development of fistula is an extremely rare complication. Previous literature has even shown an enterocolonic fistula, a vesicodiverticular fistula, ileorectal fistula, and fistula-in-ano. To the best of our knowledge, we present the first case of the fistula complicated between Meckel diverticulum and the appendix in a review of the English literature.
Insights
Meckel diverticulum, a common congenital anomaly, can rarely form a fistula. This study reports the first known case of a fistula between Meckel diverticulum and the appendix.
Area of Science:
- Gastroenterology
- Surgical Anatomy
Background:
- Meckel diverticulum is the most frequent congenital malformation of the small intestine, affecting 2%-4% of individuals.
- It arises from the incomplete obliteration of the omphalomesenteric duct.
Observation:
- Symptomatic Meckel diverticulum presents with various complications like hemorrhage, obstruction, and diverticulitis.
- Fistula formation is an exceptionally rare complication, with documented cases including enterocolonic, vesicodiverticular, ileorectal, and fistula-in-ano.
Findings:
- This paper documents the first reported instance of a fistula developing between Meckel diverticulum and the appendix.
- This unique case expands the spectrum of known Meckel diverticulum-associated fistulas.
Implications:
- Understanding this rare complication is crucial for accurate diagnosis and surgical management of Meckel diverticulum.
- This finding contributes to the anatomical and clinical knowledge of congenital gastrointestinal anomalies.
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