Small Bowel Congenital Anomalies: a Review and Update.
Publication/Presentation Date
4-1-2016
Abstract
The small intestine is a complex organ system that is vital to the life of the individual. There are a number of congenital anomalies that occur and present most commonly in infancy; however, some may not present until adulthood. Most congenital anomalies of the small intestine will present with obstructive symptoms while some may present with vomiting, abdominal pain, and/or gastrointestinal bleeding. Various radiologic procedures can aid in the diagnosis of these lesions that vary depending on the particular anomaly. Definitive therapy for these congenial anomalies is surgical, and in some cases, surgery needs to be performed urgently. The overall prognosis of congenital anomalies of the small intestine is very good and has improved with improved medical management and the advent of newer surgical modalities. The congenital anomalies of the small intestine reviewed in this article include malrotation, Meckel's diverticulum, duodenal web, duodenal atresia, jejunoileal atresia, and duplications.
Volume
18
Issue
4
First Page
16
Last Page
16
ISSN
1534-312X
Published In/Presented At
Morris, G., Kennedy, A., Jr, & Cochran, W. (2016). Small Bowel Congenital Anomalies: a Review and Update. Current gastroenterology reports, 18(4), 16. https://doi.org/10.1007/s11894-016-0490-4
Disciplines
Medicine and Health Sciences | Pediatrics
PubMedID
26951229
Department(s)
Department of Pediatrics
Document Type
Article