威廉姆斯综合征患儿的颈动脉支架移位

Carotid artery stent migration in a child with Williams syndrome.

作者信息

Yan Bryan P, Rosenfield Kenneth, Garasic Joseph M, de Moor Michael

机构信息

Cardiology Division, Section of Vascular Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

出版信息

Pediatr Cardiol. 2009 May;30(4):551-2. doi: 10.1007/s00246-009-9400-y. Epub 2009 Mar 18.

DOI:10.1007/s00246-009-9400-y

PMID:19294459

Abstract

We report a case of distal migration of a stent from the brachiocephalic artery to the distal right common carotid artery 7 months after implantation in a 5-year-old child with Williams syndrome. There were no neurological sequelae and the migrated stent remained widely patent 5 years following implantation.

摘要

我们报告了一例5岁威廉姆斯综合征患儿，在支架植入7个月后，支架从头臂动脉向右侧颈总动脉远端迁移。没有神经后遗症，且支架迁移后在植入5年时仍保持广泛通畅。