Presentation
Work up for flank pain.
Patient Data
Age: 25 years
Gender: Male
From the case:
Autosomal dominant polycystic kidney disease
{"current_user":null,"step_through_annotations":true,"access":{"can_edit":false,"can_download":true,"can_toggle_annotations":true,"can_feature":false,"can_examine_pipeline_reports":false,"can_pin":false},"extraPropsURL":"/studies/109644/annotated_viewer_json?lang=us"}
Multiple thin walled non enhanced cortical cysts are seen at both kidneys less than 38 mm; more prominent at left side.
Additionally, a few small cysts less than 5 mm are seen at liver.
The prostate gland is enlarged.
Case Discussion
Features on CT scan are most consistent with autosomal dominant polycystic kidney disease which is a common hereditary form of adult cystic renal disease and by far the most common hereditary cause of end stage renal failure.
Unable to process the form. Check for errors and try again.