Abstract
In children with biliary atresia, hepatoportoenterostomy (HP) is recommended to improve bile flow. Biliary strictures are known potential complications after HP, which can again impair bile flow often leading to biliary cirrhosis and liver transplantation. In patients who are status post HP and have biliary strictures, nonsurgical therapeutic options such as endoscopic dilation can pose technical difficulties due to altered anatomy. Percutaneous transhepatic cholangiography with cholangioplasty is a valuable tool for obstructive cholangiopathies, but to our knowledge this has not been previously demonstrated to be successful in patients with multiple intrahepatic biliary strictures status post HP. Herein, we present 3 patients status post HP who presented with multiple intrahepatic biliary strictures and underwent successful percutaneous transhepatic cholangiography with cholangioplasty.
Original language | English (US) |
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Pages (from-to) | 200-202 |
Number of pages | 3 |
Journal | Journal of pediatric gastroenterology and nutrition |
Volume | 64 |
Issue number | 2 |
DOIs | |
State | Published - Feb 1 2017 |
Keywords
- biliary atresia
- cholangitis
- choledochal cyst
- hepatoportoenterostomy
- intrahepatic biliary strictures
- percutaneous transhepatic cholangioplasty
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Gastroenterology