Oldhafer K J, Frerker M, Prokop M, Lang H, Böker K, Pichlmayr R
Division of Abdominal and Transplantation Surgery, Hannover Medical School, Germany.
Am J Gastroenterol. 1998 Jul;93(7):1165-6. doi: 10.1111/j.1572-0241.1998.363_u.x.
Budd-Chiari syndrome is characterized by hepatic venous outflow obstruction, which often leads to death as a result of portal hypertension and liver failure. Venous decompressive shunt surgery and liver transplantation represent efficient surgical treatments of Budd-Chiari syndrome. In the case presented here, severe intrahepatic compression of the inferior vena cava (IVC) was caused by the hypertrophic caudate lobe. A mere portocaval shunt was not feasible because of a large pressure gradient across the intrahepatic stenosis. A two-step procedure with preoperative radiological dilation and stenting of the intrahepatic IVC followed by a portocaval shunt was successfully performed. Consequently, liver transplantation and its subsequent immunosuppression could be avoided.
布加综合征的特征是肝静脉流出道梗阻,常因门静脉高压和肝衰竭导致死亡。静脉减压分流手术和肝移植是布加综合征有效的外科治疗方法。在本文所述病例中,肥大的尾状叶导致下腔静脉严重肝内受压。由于肝内狭窄两端存在较大压力梯度,单纯的门腔分流术不可行。成功实施了两步手术,即术前对肝内下腔静脉进行放射学扩张和支架置入,随后进行门腔分流术。因此,避免了肝移植及其后续的免疫抑制治疗。