A CASE REPORT OF CONGENITAL CYSTIC DILATATION OF INTRAHEPATIC BILIARY TREE (CAROLI’S DISEASE)
Journal Title: INTERNATIONAL ACADEMY JOURNAL "Web of Scholar" - Year 2017, Vol 1, Issue 8
Abstract
Caroli’s disease is a rare autosomal recessive congenital disorder characterized by multifocal, non-obstructive, saccular or fusiform dilatation of the large-sized intrahepatic bile ducts, which communicate with the biliary tree. . The estimated incidence of Caroli’s disease is 1 in 1 000 000 population, males and females are equally affected. The disease usually remains asymptomatic during the first 20 years, and may also remain so throughout life. The diagnosis is radiological and relies on the demonstration of continuity between the cystic lesions and the biliary tree. We report a case of Caroli’s disease, which was revealed at male patient of 44 years old.
Authors and Affiliations
Abdelalim Goher, Ya. A. Milyushina
Keywords
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