Shrestha R, Durham J D, Wachs M, Bilir B M, Kam I, Trouillot T, Everson G T
Division of Gastroenterology/Hepatology, University of Colorado School of Medicine, Denver 80262, USA.
Am J Gastroenterol. 1997 Dec;92(12):2304-6.
We report a case of fulminant hepatic failure in a 55-yr-old man due to Budd-Chiari syndrome in the setting of polycythemia rubra vera. The patient presented with acute hepatic failure, which rapidly progressed to grade IV hepatic encephalopathy. Placement of a transjugular intrahepatic portosystemic shunt resulted in marked improvement of the encephalopathy and stabilized the liver failure. Subsequently, he underwent successful nonemergent orthotopic liver transplantation. Transjugular intrahepatic portosystemic shunt placement is a safe, effective, therapeutic option to bridge patients with fulminant Budd-Chiari to liver transplantation.
我们报告一例55岁男性因真性红细胞增多症并发布加综合征导致暴发性肝衰竭的病例。患者表现为急性肝衰竭,并迅速进展为IV级肝性脑病。经颈静脉肝内门体分流术的实施使脑病明显改善,肝衰竭得以稳定。随后,他成功接受了非急诊原位肝移植。经颈静脉肝内门体分流术是一种安全、有效的治疗选择,可作为暴发性布加综合征患者肝移植的桥梁。