Autosomal Recessive Polycystic Kidney Disease with Caroli Syndrome Emmanuel C. Obusez, Unni Udayasankar  The Journal of Urology  Volume 193, Issue 2, Pages 679-680 (February 2015) DOI: 10.1016/j.juro.2014.11.013 Copyright © 2015 American Urological Association Education and Research, Inc. Terms and Conditions

Figure 1 Ultrasound in 8-year-old boy with ARPKD and Caroli syndrome. A, multiple cystic lesions of varying sizes in liver consistent with saccular dilated ducts (arrows). B, enlarged left kidney (arrows) with hyperechoic central renal sinus. The Journal of Urology 2015 193, 679-680DOI: (10.1016/j.juro.2014.11.013) Copyright © 2015 American Urological Association Education and Research, Inc. Terms and Conditions

Figure 2 Coronal HASTE (half-Fourier acquisition single-shot turbo spin-echo) MRI in 8-year-old boy with ARPKD and Caroli syndrome shows enlarged hyperintense kidneys (open arrows) due to innumerable cysts. Also note saccular and fusiform intrahepatic biliary dilatation (white arrows) typical of Caroli disease. The Journal of Urology 2015 193, 679-680DOI: (10.1016/j.juro.2014.11.013) Copyright © 2015 American Urological Association Education and Research, Inc. Terms and Conditions