Autosomal Dominant Polycystic Kidney Disease with Liver and Pancreatic Involvement.
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Date
2020-05
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Publisher
Akshantala Enterprises Private Limited
Abstract
Autosomal dominant polycystic kidney disease (adult polycystic kidney disease, Potter Type III disease) is the fourth-most common cause of end-stage renal disease.(1) Polycystic Liver Disease, the most common extrarenal manifestations of Polycystic Kidney Disease is seen in 75-90% of cases, characterized by multiple biliary cystic lesions localized in over 50% of the hepatic parenchyma. In Polycystic kidney disease, hepatic cysts develop later than the renal cysts.(2) It is associated with hypertension in about 70% of cases, cyst in pancreas in 9%, saccular berry aneurysm of cerebral arteries in 3-13%, and mitral valve prolapse.
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Soumya Jain, Suresh V. Phatak, Amruta Varma, Rajasbala P. Dhande
Citation
Jain Soumya, Phatak Suresh V., Varma Amruta, Dhande Rajasbala P.. Autosomal Dominant Polycystic Kidney Disease with Liver and Pancreatic Involvement.. Journal of Evolution of Medical and Dental Sciences. 2020 May; 9(20): 1625-1626