Hassoun Jeremy, Hammer Nathalie, Magini Giulia, Ponte Belen, Ongaro Marie, Rougemont Anne-Laure, Goossens Nicolas, Frossard Jean-Louis, Spahr Laurent
Gastroenterology and Hepatology, University Hospitals of Geneva and Faculty of Medicine, Geneva, Switzerland.
Nephrology, University Hospitals of Geneva and Faculty of Medicine, Geneva, Switzerland.
Case Reports Hepatol. 2021 May 11;2021:5583654. doi: 10.1155/2021/5583654. eCollection 2021.
Wilson's disease is a rare hereditary disorder of copper metabolism leading to progressive accumulation of copper in several organs including the brain and the liver. Acute liver failure is a relatively rare hepatic manifestation of WD which may require urgent liver transplantation if medical treatment fails. We report here the case of a young woman who presented with classic acute Wilsonian hepatitis complicated by liver and renal failure and a severe hemolysis related to massive nonceruloplasmin bound copper accumulation requiring repeated blood transfusions. The early initiation of a combined treatment including conventional chelation therapy and repeated MARS dialysis sessions allowed a rapid control of hemolysis, a progressive decrease of free copper overload, and clinical recompensation without liver transplantation.
威尔逊病是一种罕见的铜代谢遗传性疾病,会导致铜在包括脑和肝脏在内的多个器官中进行性蓄积。急性肝衰竭是威尔逊病相对罕见的肝脏表现,如果药物治疗失败,可能需要紧急进行肝移植。我们在此报告一例年轻女性病例,该患者表现为典型的急性威尔逊氏肝炎,并发肝肾功能衰竭以及与大量非铜蓝蛋白结合铜蓄积相关的严重溶血,需要反复输血。早期启动包括传统螯合疗法和反复进行分子吸附再循环系统(MARS)透析治疗的联合治疗,实现了对溶血的快速控制、游离铜过载的逐渐减轻以及无需肝移植的临床代偿。