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Cystic Bile Duct Dilatations and Caroli’s Disease

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Benign Tumors of the Liver

Abstract

Bile duct dilatations (BDD) are rare congenital anomalies of the biliary tree characterized by cystic dilatation of the common bile duct (CBD) and/or intrahepatic bile ducts. Despite the etiology is not fully understood, the presence of an anomalous biliopancreatic junction (ABPJ) is the most widely accepted etiopathogenic hypothesis. BDD are associated with cholangitis, biliary lithiasis, and risk of cholangiocarcinoma. Cholangiography in magnetic resonance is to date the most accurate preoperative imaging technique to classify the disease according to the Todani classification. Complete cyst excision with cholecystectomy followed by Roux-en-Y hepaticojejunostomy represents the gold standard treatment for the CBD component of the disease (type I and IV BDD). A cysto-enteric anastomosis is currently thought to be a dangerous and incomplete treatment. The treatment of intrahepatic bile duct dilatations remains controversial (type IVA and V BDD). A liver resection should be considered for patients in whom the impaired intrahepatic bile ducts can be completely resected after a careful evaluation of presence and severity of underlying chronic liver and kidney disease. Liver transplantation is recommended in patients with diffuse bilobar forms of the disease complicated by repeated sepsis or to patients with cirrhosis or portal hypertension. For type II BDD a limited cyst excision is recommended; CBD resection is not routinely indicated. For type III BDD the transduodenal excision is currently replaced by conservative endoscopic sphincterotomy. The risk of development of cholangiocarcinoma that can occur even after complete cyst excision justifies a careful long-term follow-up.

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Correspondence to Felice Giuliante .

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Giuliante, F., De Rose, A.M., Nuzzo, G. (2015). Cystic Bile Duct Dilatations and Caroli’s Disease. In: Aldrighetti, L., Cetta, F., Ferla, G. (eds) Benign Tumors of the Liver. Springer, Cham. https://doi.org/10.1007/978-3-319-12985-3_9

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  • DOI: https://doi.org/10.1007/978-3-319-12985-3_9

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-12984-6

  • Online ISBN: 978-3-319-12985-3

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