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布加综合征:经皮腔内血管成形术成功治疗

Budd-Chiari syndrome: successful treatment by percutaneous transluminal angioplasty.

作者信息

Fock K M, Chan C C, Khoo T K

机构信息

Department of Medicine, Toa Payoh Hospital, Singapore.

出版信息

Australas Radiol. 1993 Feb;37(1):108-10. doi: 10.1111/j.1440-1673.1993.tb00028.x.

Abstract

Budd Chiari syndrome is a rare disorder. It is caused by obstruction of the hepatic veins. The prognosis is usually dismal, except in the rare case where the obstruction is due to either webs in the hepatic veins or membranous obstruction of the inferior vena cava. Such cases, more common in the Orient, can be treated by percutaneous transluminal angioplasty. We report a case of Budd Chiari syndrome, due to a membranous obstruction in the right hepatic vein, successfully treated by percutaneous transluminal angioplasty.

摘要

布加综合征是一种罕见的疾病。它是由肝静脉阻塞引起的。除了罕见的因肝静脉内的隔膜或下腔静脉膜性阻塞导致的阻塞情况外,其预后通常很差。这种情况在东方更为常见,可通过经皮腔内血管成形术进行治疗。我们报告一例因右肝静脉膜性阻塞导致的布加综合征病例,经皮腔内血管成形术治疗成功。

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