马方综合征患儿扩张性主动脉根部的外科治疗。
Surgical treatment of the dilated aortic root in a child with Marfan's syndrome.
作者信息
Modry D L, Limacher J, Dobell A R
出版信息
Can J Surg. 1981 Sep;24(5):500-2.
PMID:7284912
Abstract
Life-threatening cardiovascular manifestations of Marfan's syndrome are rare in young children. The authors report the case of a 4 1/2-year-old girl with Marfan's syndrome who had a large aneurysm of the ascending aortic valve replaced and both coronary arteries implanted into a prosthetic graft (Bentall's procedure). Other published reports of children with aortic aneurysms due to Marfan's syndrome are reviewed.
摘要
马方综合征危及生命的心血管表现在幼儿中较为罕见。作者报告了一例4岁半患马方综合征的女孩，其升主动脉瓣巨大动脉瘤进行了置换，两条冠状动脉植入人工血管（Bentall手术）。本文还回顾了其他已发表的关于马方综合征所致儿童主动脉瘤的报告。
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