Loeys-Dietz 综合征 5 岁男童行保留瓣膜的主动脉根部和主动脉弓置换术。
Valve-sparing aortic root and aortic arch replacement in a 5-year-old boy with Loeys-Dietz syndrome.
机构信息
Department of Pediatrics, Sahloul Teaching Hospital, University of Sousse, Sousse, Tunisia.
Department of Radiology, Sahloul Teaching Hospital, University of Sousse, Sousse, Tunisia.
出版信息
Eur J Cardiothorac Surg. 2019 Aug 1;56(2):409-411. doi: 10.1093/ejcts/ezy446.
PMID:30608517
Abstract
In this study, we describe the case of a 5-year-old boy who presumably presented with Loeys-Dietz syndrome. A huge aneurysm of the ascending aorta and the aortic arch extended beyond the left subclavian artery and was accompanied by a slight narrowing of the aortic isthmus.
摘要
在本研究中，我们描述了一例 5 岁男孩，推测其患有洛伊氏迪茨综合征。升主动脉和主动脉弓的巨大动脉瘤延伸至左锁骨下动脉以外，并伴有主动脉峡部的轻微狭窄。
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