Weiss Karl Heinz, Gotthardt Daniel, Schmidt Jan, Schemmer Peter, Encke Jens, Riediger Carina, Stremmel Wolfgang, Sauer Peter, Merle Uta
Department of Gastroenterology, University of Heidelberg, Germany.
Nephrol Dial Transplant. 2007 Sep;22 Suppl 8:viii9-viii12. doi: 10.1093/ndt/gfm658.
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.
原位肝移植是许多终末期肝病并发症患者的首选治疗方法。对于代谢性肝病,肝移植不仅可以替换患病器官,还可能纠正代谢缺陷。代谢性疾病肝移植的结果令人鼓舞。在威尔逊病中,肝移植被认为是暴发性和终末期肝病的有效治疗方法,长期疗效极佳。然而,对于有严重神经功能障碍的威尔逊病患者是否应考虑肝移植仍存在争议。遗传性血色素沉着症的肝移植相对少见,且与移植后患者生存率降低有关,最可能的原因是感染和心脏并发症。遗传性血色素沉着症患者在肝移植前减轻铁过载可能会有更好的预后。