Torres E A, Altieri A, Tellado M
Department of Medicine, University of Puerto Rico School of Medicine.
Bol Asoc Med P R. 1990 Jun;82(6):266-8.
A 21 y/o female presented with fulminant hepatic failure and hemolysis. On the basis of the clinical presentation, levels of ceruloplasmin and serum copper a presumptive diagnosis of Wilson's disease was made. In spite of supportive measures and hemodialysis, the patient died one week after admission. Postmortem examination showed cirrhosis and increased copper stores in the liver, corroborating the clinical diagnosis of Wilson's disease. Study of the four siblings revealed that two are carriers, one is healthy and one may have the disease. Wilson's disease is a rare cause of fulminant hepatic failure that must be suspected specially when hemolysis is associated to the clinical picture. This mode of presentation is virtually fatal and early liver transplantation is the best form of therapy.
一名21岁女性出现暴发性肝衰竭和溶血。根据临床表现、血浆铜蓝蛋白水平和血清铜,初步诊断为威尔逊病。尽管采取了支持措施和血液透析,患者在入院一周后死亡。尸检显示肝硬化和肝脏铜储存增加,证实了威尔逊病的临床诊断。对其四个兄弟姐妹的研究发现,两人为携带者,一人健康,一人可能患有该病。威尔逊病是暴发性肝衰竭的罕见病因,特别是当溶血与临床表现相关时必须怀疑该病。这种表现形式几乎是致命的,早期肝移植是最佳治疗方式。