| Literature DB >> 28340841 |
S Acar1, G Gencdal2, M Tokac3, E Eren3, U Alkara4, G Tellioglu3, A Dinckan3, M Akyildiz5.
Abstract
Polycystic liver disease is characterized by multiple cystic lesions on the liver. It is an uncommon autosomal dominant disease. The cysts' diameters range from 20 to 30 cm to small microscopic nodules. Generally, more than half of the liver parenchyma is covered. The mass effect of the liver created by the large cysts can cause life-threatening symptoms such as weight loss, reduction of oral intake, and malnutrition. Liver transplantation is the best treatment option in symptomatic patients. We present a patient who had polycystic liver and kidney disease, and we performed liver transplantation because of his life-threatening symptoms.Entities:
Mesh：
Year: 2017 PMID： 28340841 DOI： 10.1016/j.transproceed.2017.01.033
Source DB: PubMed Journal: Transplant Proc ISSN： 0041-1345 Impact factor: 1.066