抗凝血酶III缺乏所致的布加综合征
Budd-Chiari syndrome due to antithrombin III deficiency.
作者信息
Jagtap Amit, Shanbag Preeti, Vaidya Mamta
机构信息
Department of Pediatrics, Lokmanya Tilak Medical College & General Hospital, Sion, Mumbai, India.
出版信息
Indian J Pediatr. 2003 Dec;70(12):1003-5. doi: 10.1007/BF02723831.
PMID:14719794
Abstract
Budd-Chiari syndrome is a disease complex with varied etiology and is one of the causes of post-hepatic portal hypertension. We report a 2 year-old boy who presented with Budd-Chiari syndrome due to congenital antithrombin III deficiency, who was managed with an expandable metal stent placed in the inferior vena cava and oral anticoagulation.
摘要
布加综合征是一种病因多样的疾病复合体，是肝后性门静脉高压的病因之一。我们报告一名2岁男孩，因先天性抗凝血酶III缺乏而出现布加综合征，通过在下腔静脉放置可扩张金属支架及口服抗凝药物进行治疗。
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