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复杂先天性主动脉瓣狭窄的外科治疗。左心室流出道三级梗阻合并二尖瓣关闭不全、主动脉缩窄及预激综合征。

Surgical treatment for a complicated congenital aortic stenosis. The association of a three-level obstruction of the left ventricular outflow tract with mitral incompetence, coarctation of the aorta, and the Wolff-Parkinson-White syndrome.

作者信息

Vanetti A, Donzeau-Gouge P, Frank R, Fourati M, Evans J, Ismail M B, Daumet P

出版信息

J Thorac Cardiovasc Surg. 1979 Feb;77(2):230-3.

PMID:762963
Abstract

We report a case of complex congenital aortic stenosis with obstruction at all three levels of the left ventricular outflow tract (subaortic, aortic, and supravalvular aortic stenoses) associated with a mitral malformation, coarctation of the aorta, and the Wolff-Parkinson-White syndrome. The subaortic stenosis was corrected by excision and myotomy, and the supravalvular stenosis by a widening prosthetic operation with a Dacron patch extending as far as the aortic ring, at which level a Björk-Shiley No. 17 aortic prosthesis was inserted. The mitral valve was replaced by a Lillehei-Kaster prosthesis. The coarctation of the aorta was not significant and was left alone. Permanent pacing was needed because of peroperative surgical section of the bundle of His. Reviews of the literature and the various techniques used to widen the left ventricular outflow tract are included.

摘要

我们报告了一例复杂的先天性主动脉狭窄病例,其左心室流出道的三个层面(主动脉瓣下、主动脉瓣及主动脉瓣上狭窄)均存在梗阻,并伴有二尖瓣畸形、主动脉缩窄及预激综合征。主动脉瓣下狭窄通过切除和心肌切开术矫正,主动脉瓣上狭窄则采用加宽修复手术,用涤纶补片一直延伸至主动脉环,在此处植入了一枚型号为17的Björk-Shiley主动脉瓣假体。二尖瓣被Lillehei-Kaster假体所置换。主动脉缩窄不严重,未作处理。由于术中希氏束被切断,因此需要进行永久性起搏。文中还包括了对文献的综述以及用于加宽左心室流出道的各种技术。

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