First living donor liver transplantation for congenital hepatic fi brosis in Azerbaijan
https://doi.org/10.23873/2074-0506-2017-9-2-113-117
Abstract
Congenital hepatic fibrosis is a rare autosomal recessive disease. Only a few such cases have been described worldwide, but the exact incidence of the disease is unknown. The diagnosis is sometimes difficult to establish and one of the main diagnostic method is the histological evaluation. The management and prognosis of congenital hepatic fibrosis is dependent on alimentary tract bleeding secondary to portal hypertension. In late childhood, the abdominal pain, cholangitis, and features of hypersplenism complicate the problem. Herein we present the case report of patient with congenital hepatic fibrosis. Our choice of treatment was the living donor liver transplantation. This procedure is very difficult but it is the only life-saving option for the patients with congenital hepatic fibrosis.
About the Authors
R. A. MamedovAzerbaijan
Cand. Med. Sci., Head of the Transplantology Department at Teaching Surgical Clinic of Azerbaijan Medical University, Baku, Republic of Azerbaijan
N. Yu. Bayramov
Azerbaijan
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Review
For citations:
Mamedov R.A., Bayramov N.Yu. First living donor liver transplantation for congenital hepatic fi brosis in Azerbaijan. Transplantologiya. The Russian Journal of Transplantation. 2017;9(2):113-117. (In Russ.) https://doi.org/10.23873/2074-0506-2017-9-2-113-117