The Case | Atypical cysts in a patient with autosomal dominant polycystic kidney disease

A 41-year-old female patient from Afghanistan was referred to our hospital because of multiple cysts in both liver and kidneys accompanied by recurrent left flank pain and hematuria. Despite inconclusive family history, the patient was suspected of suffering from autosomal dominant polycystic kidney disease (ADPKD) on the basis of a medical history of adult-onset polycystic kidneys. Abdominal ultrasound revealed multicystic liver and kidneys...