Jagtap Amit, Shanbag Preeti, Vaidya Mamta
Department of Pediatrics, Lokmanya Tilak Medical College & General Hospital, Sion, Mumbai, India.
Indian J Pediatr. 2003 Dec;70(12):1003-5. doi: 10.1007/BF02723831.
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.
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。
