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2021
Caroli’s disease (CD) is a rare autosomic recessive congenital pathology that belongs to the spectrum of fibro-polycystic liver disease, a group of entities caused by an abnormal embryologic development of the ductal plate. CD is characterized by non-obstructive dilatations of the large intrahepatic bile ducts that communicate with the biliary system ...
Raffaella Motta +4 more
openaire +1 more source
Caroli’s disease (CD) is a rare autosomic recessive congenital pathology that belongs to the spectrum of fibro-polycystic liver disease, a group of entities caused by an abnormal embryologic development of the ductal plate. CD is characterized by non-obstructive dilatations of the large intrahepatic bile ducts that communicate with the biliary system ...
Raffaella Motta +4 more
openaire +1 more source
Acta medica Croatica : casopis Hravatske akademije medicinskih znanosti, 2003
Caroli's disease is a rare condition characterized by congenital polycystic dilatation of the intrahepatic bile ducts. The most frequent clinical presentation of a simple type (Caroli's disease) is recurrent cholangitis, gallstone with pain, obstructive jaundice and episodes of pancreatitis in childhood and early adulthood.
Marko, Duvnjak +4 more
openaire +1 more source
Caroli's disease is a rare condition characterized by congenital polycystic dilatation of the intrahepatic bile ducts. The most frequent clinical presentation of a simple type (Caroli's disease) is recurrent cholangitis, gallstone with pain, obstructive jaundice and episodes of pancreatitis in childhood and early adulthood.
Marko, Duvnjak +4 more
openaire +1 more source
Ugeskrift for laeger, 1996
Caroli's disease (CS) is a rare malformation of the bile duct with multiple segmental communicating dilatations of intrahepatic bile ducts affecting the whole of or parts of the liver. The disease is presumably of autosomal recessive hereditary character.
F M, Johnsen +3 more
openaire +1 more source
Caroli's disease (CS) is a rare malformation of the bile duct with multiple segmental communicating dilatations of intrahepatic bile ducts affecting the whole of or parts of the liver. The disease is presumably of autosomal recessive hereditary character.
F M, Johnsen +3 more
openaire +1 more source
Surgical Management of Caroli’s Disease: Single Center Experience and Review of the Literature
Journal of Gastrointestinal Surgery, 2015Michael Cruise +2 more
exaly
Liver transplantation in patients with Caroli's disease and recurrent cholangitis
Transplant International, 1997A Rimola
exaly