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[威廉姆斯综合征合并主动脉瓣上狭窄的扩大主动脉成形术]

[Extended aortoplasty for supravalvular aortic stenosis with Williams syndrome].

作者信息

Nagasaka S, Taniguchi S, Kawata T, Mizuguchi K, Kawachi K, Kitamura S

机构信息

Department of Surgery III, Nara Medical College, Japan.

出版信息

Nihon Kyobu Geka Gakkai Zasshi. 1997 Apr;45(4):601-6.

PMID:9155132
Abstract

We report a male case of supravalvular aortic stenosis associated with Williams syndrome requiring surgery at age 11. At 5 years of age, this boy presented with a harsh systolic heart murmur and was diagnosed as having a supravalvular aortic stenosis. In association with mental retardation, elfin face and bilateral inguinal hernias, he was diagnosed as a Williams syndrome confirmed by the chromosomal analysis revealing the deletion of 7q11.23. The pressure gradient across the stenotic lesion of the ascending aorta, which had been 35 mmHg at age 5, progressed to 80 mmHg at age 11 years. Extended aortoplasty was performed using a patch of 20 mm Hemashield graft prosthesis. Postoperative cardiac catheterization confirmed that the pressure gradient in the ascending aorta completely disappeared following surgery.

摘要

我们报告一例患有威廉姆斯综合征的男性主动脉瓣上狭窄病例,该患者11岁时需要接受手术治疗。该男孩5岁时出现粗糙的收缩期心脏杂音,被诊断为主动脉瓣上狭窄。伴有智力发育迟缓、小精灵面容和双侧腹股沟疝,经染色体分析显示7q11.23缺失,确诊为威廉姆斯综合征。升主动脉狭窄病变处的压力阶差在5岁时为35 mmHg,到11岁时进展至80 mmHg。使用一片20 mm的Hemashield移植人工血管进行了扩大主动脉成形术。术后心导管检查证实,术后升主动脉的压力阶差完全消失。

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