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Two Cases of Intraluminal “Windsock” Diverticula Resulting in Partial Duodenal Obstruction

An intraluminal duodenal diverticulum (IDD) is a rare congenital anomaly that is the result of incomplete recanalization of the embryologic foregut leaving a fenestrated membrane within the lumen of the duodenum. Years of peristalsis acting on the membrane result in the formation of a diverticulum....

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Detalles Bibliográficos
Autores principales: Anand, Vikram, Provost, Justin, Bakr, Maged, Bach, Christopher, Merchant, Prakriti, Brown, Christopher, Gruss, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American College of Gastroenterology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062679/
https://www.ncbi.nlm.nih.gov/pubmed/27807587
http://dx.doi.org/10.14309/crj.2016.108
Descripción
Sumario:An intraluminal duodenal diverticulum (IDD) is a rare congenital anomaly that is the result of incomplete recanalization of the embryologic foregut leaving a fenestrated membrane within the lumen of the duodenum. Years of peristalsis acting on the membrane result in the formation of a diverticulum. Most patients are asymptomatic, while some may have abdominal pain, bloating, or fullness. Rare complications include gastrointestinal bleeding, obstruction, pancreatitis, and cholangitis. We present 2 cases with endoscopic findings consistent with partially obstructing symptomatic IDD.