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The place of liver transplantation in Caroli's disease and syndrome

✍ Scribed by Laurent De Kerckhove; Martine De Meyer; Catherine Verbaandert; Michel Mourad; Etienne Sokal; Pierre Goffette; Andre Geubel; Vincent Karam; Rene Adam; Jan Lerut

Book ID
110916664
Publisher
Springer
Year
2006
Tongue
English
Weight
282 KB
Volume
19
Category
Article
ISSN
0934-0874

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Caroli's disease is a rare indication for liver transplantation that accounts for 0.13% of all liver transplants performed in the United States. 1 It was first described in 1958 by the French physician Jacques Caroli (1902-1979). 2 The disease is characterized by segmental dilatation of the intrahep

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Caroli's disease is a rare congenital hepatic disease, characterized by segmental dilatation of the biliary tree. Patients who have recurrent bouts of biliary infection, particularly those with complications related to portal hypertension, may require orthotopic liver transplantation (OLT). Few case

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Caroli's disease is a rare autosomal recessive disorder characterized by intrahepatic cystic dilatation of the bile ducts that, when progressive, leads to intrahepatic stones, recurrent cholangitis, portal hypertension, cholangiocarcinoma, and liver failure. Liver transplantation is a promising cura