]> 2026-07-31T09:41:32+00:00 WBR0415 0 en Large hepatic multiacinar regenerative nodules Granulomatous inflammation and skip lesions in a bowel segment Cranial nerve compression by an adjacent structure Autosomal (adult) dominant polycystic kidney disease (ADPKD) is an inherited renal disorder characterized by the development of fluid-filled cysts in both kidneys during adulthood. It is associated with the development of berry aneurysms, which may cause mechanical compression of the nearby CN III in the event of development of posterior communicating artery aneurysm. Granulomatous inflammation of a great vessel Obliteration of the biliary tree Pathology C Renal 2020-10-28T00:29:38Z 2459150.5205787 WBR0415