Colonic duplication is a rare abnormality, comprising only 6�7 of all gastrointestinal duplications and usually present during the first decade of life. Tubular duplications of the sigmoid colon are extremely rare and only a few cases have been reported in the literature. In this study, we report the case of a 27-year-old rural man visited our hospital with symptom of repeated episodes of abdominal pain in epigastric region that radiated to right flank and back. An abdominal computed tomography (CT) scan with oral and intravenous contrast revealed an extremely dilated and air-filled loop related to sigmoid colon. An exploratory laparotomy was performed and tubular sigmoid colon duplication was found intraoperatively. The postoperative p...
Copyright © 2012 Abhishek Shah et al. This is an open access article distributed under the Creative ...
Complete colonic duplication is rare and frequently asymptomatic. We present an interesting case of ...
Journal Article;We report the case of a 6-month-old infant who presented with a complete duplication...
Gastrointestinal tract duplication is a rare congenital anomaly that can occur anywhere along the al...
Background: Intestinal duplications are rare congenital developmental anomalies with an incidence of...
Total colonic duplications are rare. This case is reported here in order to discuss the treatment of...
Colonic duplication is a rare congenital anomaly of the alimentary tract. In most cases, symptomatic...
Gatrointestinal duplications are rare congenital anomalies, usually detected prenatally or in the fi...
Gatrointestinal duplications are rare congenital anomalies, usually detected prenatally or in the fi...
Enteric duplications (EDs) are rare congenital anomalies that result from defect during embryonic de...
Tubular duplication of the colon is very rare especially in adulthood, because it is frequently symp...
Alimentary tract duplications are rare congenital malformations that occur most commonly in the jeju...
Complete colonic duplication is a very rare congenital anomaly that may have different presentations...
BackgroundDuplication of the transverse colon is a rare gastrointestinal malformation. Its pathogene...
Intestinal duplication in an adult is an uncommon congenital abnormality because only minority of ca...
Copyright © 2012 Abhishek Shah et al. This is an open access article distributed under the Creative ...
Complete colonic duplication is rare and frequently asymptomatic. We present an interesting case of ...
Journal Article;We report the case of a 6-month-old infant who presented with a complete duplication...
Gastrointestinal tract duplication is a rare congenital anomaly that can occur anywhere along the al...
Background: Intestinal duplications are rare congenital developmental anomalies with an incidence of...
Total colonic duplications are rare. This case is reported here in order to discuss the treatment of...
Colonic duplication is a rare congenital anomaly of the alimentary tract. In most cases, symptomatic...
Gatrointestinal duplications are rare congenital anomalies, usually detected prenatally or in the fi...
Gatrointestinal duplications are rare congenital anomalies, usually detected prenatally or in the fi...
Enteric duplications (EDs) are rare congenital anomalies that result from defect during embryonic de...
Tubular duplication of the colon is very rare especially in adulthood, because it is frequently symp...
Alimentary tract duplications are rare congenital malformations that occur most commonly in the jeju...
Complete colonic duplication is a very rare congenital anomaly that may have different presentations...
BackgroundDuplication of the transverse colon is a rare gastrointestinal malformation. Its pathogene...
Intestinal duplication in an adult is an uncommon congenital abnormality because only minority of ca...
Copyright © 2012 Abhishek Shah et al. This is an open access article distributed under the Creative ...
Complete colonic duplication is rare and frequently asymptomatic. We present an interesting case of ...
Journal Article;We report the case of a 6-month-old infant who presented with a complete duplication...