Imaging of ARPKD
Autosomal recessive polycystic kidney disease (ARPKD) is often first suspected at prenatal or neonatal ultrasound. Imaging features include enlarged, echogenic kidneys, with poor corticomedullary differentiation, often without discretely discernible cysts. If a linear (high frequency) probe is used, small tubular cysts can be seen, which are the ectatic collecting ducts.
Hepatic fibrosis and biliary abnormalities are associated with ARPKD, and these can also be seen on ultrasound. In patients with severe hepatic fibrosis, splenomegaly and portosystemic varices may also be present.
Case courtesy of Dr Alexandra Stanislavsky, Radiopaedia.org, rID: 14079. Enlarged, echogenic kidneys with poor corticomedullary differentiation in a neonate who had previously had oligohydramnios on prenatal ultrasound. A few discrete cysts are present.












