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A Case of Congenital Common Bile Duct Web Treated with Balloon Dilation under Endoscopic Retrograde Cholangiopancreatography in a Young Childopen access

Authors
Park, Ji SookKim, Hong JunSeo, Ji-HyunYoun, Hee-Shang
Issue Date
Mar-2021
Publisher
KOREAN SOC GASTROINTESTINAL ENDOSCOPY
Keywords
Common bile duct; Congenital; Endoscopic retrograde cholangiopancreatography; Web
Citation
CLINICAL ENDOSCOPY, v.54, no.2, pp 285 - 288
Pages
4
Indexed
SCOPUS
ESCI
KCI
Journal Title
CLINICAL ENDOSCOPY
Volume
54
Number
2
Start Page
285
End Page
288
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/4005
DOI
10.5946/ce.2020.167
ISSN
2234-2400
2234-2443
Abstract
Web in common bile duct (CBD web) is very rare. It is usually asymptomatic and detected incidentally during surgery for other causes in adults. It can be congenital or acquired, however congenital CBD web is extremely rare. Currently, despite its invasiveness and complications, endoscopic retrograde cholangiopancreatography (ERCP) is considered as a useful diagnostic and therapeutic modality in children with hepatobiliary pancreatic diseases as in adults. Herein we report a case of congenital CBD web presenting with acute pancreatitis and choledocholithiasis in a 4-year-old girl which was diagnosed and treated using balloon dilation under ERCP. After balloon dilation of the web, a common pancreatobiliary channel was observed. To the best of our knowledge, a case of congenital CBD web with pancreatobiliary junctional abnormality treated using ERCP in a child has not been reported to date.
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