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一名儿童因下腔静脉膜状蹼导致布加综合征,经全身及局部重组组织型纤溶酶原激活剂治疗后痊愈。

Budd-Chiari syndrome in a child due to a membranous web of the inferior vena cava resolved by systemic and local recombinant tissue plasminogen activator treatment.

作者信息

Alioğlu Bülent, Avci Zekai, Aytekin Cüneyt, Mercan Sükrü, Ozçay Figen, Kürekçi Emin, Ozbek Namk

机构信息

Department of Pediatric Hematology, Baskent University Faculty of Medicine, Ankara, Turkey.

出版信息

Blood Coagul Fibrinolysis. 2006 Apr;17(3):209-12. doi: 10.1097/01.mbc.0000220244.12412.0b.

Abstract

Budd-Chiari syndrome is a heterogeneous group of disorders characterized by hepatic venous outflow obstruction. Although there are no guidelines for treatment of patients with Budd-Chiari syndrome, thrombolytic therapy may be useful in patients with acute Budd-Chiari syndrome. In this report, a boy with Budd-Chiari syndrome due to membranous obstruction of the inferior vena cava treated with systemic and local administration of recombinant tissue plasminogen activator is described. We would like to emphasize the role of systemic and local fibrinolytic treatment in these patients.

摘要

布加综合征是一组以肝静脉流出道梗阻为特征的异质性疾病。尽管目前尚无布加综合征患者的治疗指南,但溶栓治疗可能对急性布加综合征患者有用。在本报告中,描述了一名因下腔静脉膜性梗阻导致布加综合征的男孩,接受了重组组织型纤溶酶原激活剂的全身和局部给药治疗。我们想强调全身和局部纤溶治疗在这些患者中的作用。

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