Living donor liver transplantation for more than 30-year survived patients with native liver after Kasai operation for biliary atresia
نویسندگان
چکیده
منابع مشابه
Living donor liver transplantation for biliary atresia.
Biliary atresia is the most common cause of chronic cholestasis in infants and children. The incidence is estimated at 3.7:10,000 among Taiwanese infants. Kasai hepatoportoenterostomy helps children survive beyond infancy. Liver transplantation is indicated when the Kasai procedure fails to work or when patients develop progressive deterioration of liver function despite an initially successful...
متن کاملPortal vein thrombosis in biliary atresia patients after living donor liver transplantation.
BACKGROUND Vascular complications are major complications after living donor liver transplantation (LDLT), especially in biliary atresia (BA). Early diagnosis and treatment of portal vein thrombosis (PVT) may ensure optimal graft function and good recipient survival. Our aim was to find any association between pre- and post-transplant anatomic characteristics and hemodynamics, and the occurrenc...
متن کاملLiver transplantation for biliary atresia.
Biliary atresia is the most common indication for liver transplantation (OLT) in children. We present our experience with OLT as a treatment for end-stage liver disease in children with biliary atresia. We performed a retrospective review of 20 biliary atresia patients (11 male, 9 female patients; mean age, 21.4 months; range, 6 to 84 months) who had undergone OLT. Mean preoperative weight and ...
متن کاملLiver Transplantation for Biliary Atresia*
tried, but with little success, and many do not recommend it because even in adult cases where carcinoma is the underlying obstructive factor, the result obtained with the Longmire procedure is invariably poor and short-lived. The final cure will ultimately be in the hands of the geneticist, who must prophylactically reduce the number of congenital atresia cases that come before the surgeon. Fi...
متن کاملLiving donor liver transplantation for biliary atresia: a single-center experience with first 100 cases.
The aim of this study is to present our institutional experience in living donor liver transplantation (LDLT) as a treatment for end-stage liver disease in children with biliary atresia (BA). A retrospective review of transplant records was performed. One hundred BA patients (52 males and 48 females) underwent LDLT. The mean follow-up period was 85.5 months. The mean age was 2.4 years. The mean...
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ژورنال
عنوان ژورنال: Transplantation Reports
سال: 2020
ISSN: 2451-9596
DOI: 10.1016/j.tpr.2020.100052