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Autosomal dominant polycystic kidney disease and transplantation

Mariusz Niemczyk, Stanisław Niemczyk, Leszek Pączek

Ann Transplant 2009; 14(4): 86-90

ID: 880560

Published: 2009-12-09


Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder affecting 1 in 1,000 people and responsible for 10% of cases of the end stage renal disease (ESRD). Apart from renal manifestations, changes in other organs may be present. In the absence of contraindications, patients with ADPKD and ESRD should be reffered to renal transplantation. The ADPKD patient may also need liver transplantation, or combined liver and kidney transplantation. Also, the patient with ADPKD may become a potential organ donor. The aim of our paper is to review the problems that the physicians deal with in ADPKD patients in pre- and post-transplant period.

Keywords: autosomal dominant polycystic kidney disease, Kidney Transplantation, Liver Transplantation, complications



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