Kumada Y, Yasuda H, Sasaki E, Murakawa S, Mori Y, Hirose H
First Department of Surgery, Gifu University, Japan.
Jpn J Thorac Cardiovasc Surg. 1998 Oct;46(10):1061-4. doi: 10.1007/BF03217875.
A case of diffuse supravalvular aortic stenosis (SVAS) with Williams syndrome is reported. In this case of severe diffuse SVAS, we performed the diamond-patch aortoplasty in a child. However he has been suffering from residual SVAS. At 9-years old, the myocardial injury was noted by myocardial scintigraphy. Preoperative cardiac catheterization and angiography revealed the hypoplastic ascending aorta and arch with a pressure gradient of 89 mmHg at the distal site from the left subclavian artery. Through only a median stenotomy, an extended patch aortoplasty between the valsalva sinus and distal arch was performed and an extraanatomic bypass from the ascending aorta to the descending aorta was employed using a 10 mm tube graft. We realize this technique is available because this method can relieve the left ventriculus of the pressure load and operate via only median sternotomy.
报告了一例患有威廉姆斯综合征的弥漫性主动脉瓣上狭窄(SVAS)病例。在这个严重弥漫性SVAS病例中,我们为一名儿童实施了菱形补片主动脉成形术。然而,他仍患有残余的SVAS。9岁时,心肌闪烁显像显示有心肌损伤。术前心脏导管检查和血管造影显示升主动脉和主动脉弓发育不全,在左锁骨下动脉远端部位的压力梯度为89 mmHg。仅通过正中胸骨切开术,在主动脉窦和远端主动脉弓之间进行了扩大补片主动脉成形术,并使用10 mm人工血管从升主动脉到降主动脉进行了解剖外旁路移植。我们认识到这种技术是可行的,因为这种方法可以减轻左心室的压力负荷,并且仅通过正中胸骨切开术进行手术。