Copyright
©The Author(s) 2022.
World J Gastrointest Pharmacol Ther. Jul 5, 2022; 13(4): 33-46
Published online Jul 5, 2022. doi: 10.4292/wjgpt.v13.i4.33
Published online Jul 5, 2022. doi: 10.4292/wjgpt.v13.i4.33
Type | Description |
Type I | Cystic dilatation of the common bile duct. Also cysts there may be at extrahepatic right and left hepatic ducts and at common hepatic ducts. Intrahepatic bile ducts are unaffected |
Type Ia | Large saccular cystic dilatation of the common bile duct, with dilatation of the common hepatic duct and the right and left hepatic duct |
Type Ib | Focal and segmental dilation of the common bile duct |
Type Ic | Diffuse fusiform dilation of the common bile duct |
Type II | Common bile duct diverticulum |
Type III | Cysts in the intraduodenal part of the common bile duct – known as choledochocele |
Type IV | Multiple extrahepatic alone, or multiple extrahepatic and intrahepatic cysts together |
Type IVa | Extrahepatic and intrahepatic cysts |
Type IVb | Multiple extrahepatic cysts (common hepatic duct, common bile duct and intraduodenal common bile duct) |
Type V | One or more cystic dilatation of the intrahepatic bile duct. Multiple intrahepatic bile duct cysts are defined as Caroli disease |
- Citation: Islek A, Tumgor G. Biliary atresia and congenital disorders of the extrahepatic bile ducts. World J Gastrointest Pharmacol Ther 2022; 13(4): 33-46
- URL: https://www.wjgnet.com/2150-5349/full/v13/i4/33.htm
- DOI: https://dx.doi.org/10.4292/wjgpt.v13.i4.33