Caroli's Syndrome with Autosomal Recessive Polycystic Kidney Disease in a Two Month Old Infant

نویسندگان

  • Jeong Tae Kim
  • Yoon Jeong Hur
  • Jee Min Park
  • Myung Joon Kim
  • Young Nyun Park
  • Jae Seung Lee
چکیده

Caroli's syndrome is a rare congenital disorder that involves intrahepatic bile duct ectasia and congenital hepatic fibrosis, frequently seen with concomitant autosomal recessive polycystic kidney disease (ARPKD). Literature on infants with ARPKD is rare. Here, we present a case of a two month old boy who was diagnosed with Caroli's syndrome and ARPKD.

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منابع مشابه

Caroli's Syndrome in a Post Renal Transplant Patient: Case Report and Review of the Literature

Caroli's syndrome is characterized by bile duct ectasia in association with hepatic fibrosis. It is usually transmitted in an autosomal recessive fashion and has been well documented to be associated with autosomal recessive polycystic kidney disease and occasionally with autosomal dominant polycystic kidney disease. However, there has been only few case reports published with Caroli's syndrome...

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Liver Cysts and Abscesses

Ductal cysts. Choledochal cysts: a congenital dilatation of part or whole of the common bile duct. See separate article Choledochal Cysts. Cysts related to Caroli's disease: Caroli's disease is the combination of cystic dilatation of the intrahepatic bile ducts and infantile polycystic kidney disease. It has autosomal recessive inheritance. It can present with fever, abdominal pain and recurren...

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عنوان ژورنال:

دوره 47  شماره 

صفحات  -

تاریخ انتشار 2006