Liver transplantation for metabolic liver diseases in adults: indications and outcome

被引:10
作者
Weiss, Karl Heinz
Gotthardt, Daniel
Schmidt, Jan
Schemmer, Peter
Encke, Jens
Riediger, Carina
Stremmel, Wolfgang
Sauer, Peter
Merle, Uta
机构
[1] Univ Hosp Heidelberg, Dept Gastroenterol, D-69120 Heidelberg, Germany
[2] Univ Hosp Heidelberg, Dept Surg, D-69120 Heidelberg, Germany
关键词
haemochromatosis; liver transplantation; metabolic diseases; Wilson's disease; HEPATIC IRON OVERLOAD; WILSONS-DISEASE; HEREDITARY HEMOCHROMATOSIS; CLINICAL PRESENTATION; DIAGNOSIS; FAILURE; EXPERIENCE; SURVIVAL; MANAGEMENT; CIRRHOSIS;
D O I
10.1093/ndt/gfm658
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Orthotopic liver transplantation is the preferred treatment for many patients with complications of end-stage liver disease. For metabolic liver diseases liver transplantation does not only replace the diseased organ, but also can potentially correct the metabolic defect. Results of liver transplantation for metabolic diseases have been encouraging. In Wilson's disease liver transplantation is considered an effective treatment for the fulminant form and for end-stage liver disease, associated with an excellent long-term outcome. However, it is still a matter of controversy whether liver transplantation should be considered in Wilson's disease patients with severe neurological impairment. Liver transplantation for hereditary haemochromatosis is relatively uncommon and is associated with a decreased post-transplantation patient survival, most likely due to infections and cardiac complications. Reduction of iron overload prior to liver transplantation in patients with hereditary haemochromatosis might be associated with a better outcome.
引用
收藏
页码:9 / 12
页数:4
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