Unsuspected bile duct paucity in donors for living-related liver transplantation: Two case reports

被引:23
作者
Gurkan, A
Emre, S
Fishbein, TM
Brady, L
Millis, M
Birnbaum, A
Kim-Schluger, L
Sheiner, PA
机构
[1] Mt Sinai Med Ctr, Recanati Miller Transplantat Inst, New York, NY 10029 USA
[2] Univ Chicago, Childrens Hosp, Dept Pediat, Chicago, IL 60637 USA
[3] Univ Chicago, Childrens Hosp, Dept Surg, Chicago, IL 60637 USA
关键词
D O I
10.1097/00007890-199902150-00013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Alagille's syndrome is a common cause of liver dis ease in children and may lead to the need for orthotopic liver transplantation Alagille's syndrome is inherited in an autosomal dominant manner, with variable penetration, and may also be present in patients' parents, who may be considered potential donors for living-related transplantation We report here on two cases in which the living-related donors for children with Alagille's syndrome had no Liver function abnormalities or characteristic features of Alagille's syndrome. In both cases, the operation for living-related donation had to be aborted because of a paucity of bile ducts discovered intraoperatively. Given the variable presentation of Alagille's syndrome, we believe that it is necessary preoperatively to evaluate the biliary system of family members who are potential living-related donors for patients with this condition.
引用
收藏
页码:416 / 418
页数:3
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