Patch aortoplasty for supravalvular aortic stenosis with bicuspid aortic valve associated with Williams syndrome

M. Tiwari, A. Verma, A. Hooda, R. Yadav, Ranjendra Mohan Mathur, C. Shrivastava
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Abstract

We experienced a case in which a 7-year-old boy with a characteristic elfin face, heart murmur, and mental retardation, underwent extended patch aortoplasty using diamond shaped dacron patch for congenital supravalvular aortic stenosis. The aortography performed before operation demonstrated diffuse stenosis just above the aortic valve, which was a typical hourglass type. The preoperative peak systolic pressure gradient between the left ventricle and ascending aorta was 86 mmHg, and was improved postoperatively. In this procedure no cusp was incised, resulting in no deformity of the aortic valve and no obstruction of coronary arteries. In conclusion this method was excellent for the diffuse type of supravalvular aortic stenosis.
瓣上主动脉瓣狭窄伴二尖瓣主动脉瓣成形术治疗威廉姆斯综合征
我们经历了一个7岁的男孩,他有一个典型的小精灵脸,心脏杂音和智力低下,使用钻石形状的涤纶补片进行了先天性瓣上主动脉狭窄的扩展修补术。术前主动脉造影显示主动脉瓣上方弥漫性狭窄,为典型的沙漏型。术前左心室与升主动脉间收缩压梯度峰值为86 mmHg,术后有所改善。在这个过程中,没有切尖,没有导致主动脉瓣畸形和冠状动脉阻塞。结论:该方法对弥漫性瓣上主动脉狭窄有较好的疗效。
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