Mar 18, 2025 · Caroli syndrome, also known as type 2 Caroli disease, is defined by intrahepatic ductal dilatation and congenital hepatic fibrosis, and is classified as type V in the Todani …

Caroli disease (communicating cavernous ectasia, or congenital cystic dilatation of the intrahepatic biliary tree) is a rare inherited disorder characterized by cystic dilatation (or …

This entity is further divided into two subtypes: Simple Caroli's disease and complex type associated with congenital hepatic fibrosis also known as Caroli's syndrome. It has an …

Jun 26, 2015 · Caroli's disease is a rare autosomal-recessive disorder caused by malformation of the ductal plate during embryonic development. Although it is present at birth, Caroli's disease …

Both Caroli disease (CD) and autosomal recessive polycystic kidney disease (ARPKD) are autosomal recessive disorders, which are more commonly found in infants and children, for …

Caroli syndrome, also known as type 2 Caroli disease, is de-fined by intrahepatic ductal dilatation and congenital hepatic fibrosis, and is classified as type V in the Todani classification of …

Mar 20, 2020 · Three-dimensional reconstructions from T2-weighted magnetic resonance images of 35-week fetus diagnosed with Caroli's disease with autosomal recessive polycystic kidney …

Dec 26, 2024 · Coronal MRI T2-weighted fat-saturated (c) images show T2-weighted hyperintense lesion (arrow) infiltrating along the bile ducts. MR cholangiopancreatography …

We under-took this study to reevaluate the radiologic features of Caroli’s disease, with an empha-sis on reporting the spectrum of the features of the disease and the correlation with gross and …

Caroli disease (CD) is a condition in which there are multiple cystic dilations of the bile ducts within the liver that are present from birth. In this case report, we present the imaging findings …