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Aorto-Pulmonary Window, an Unrecognized Cause of Heart Failure in Infants: A Case Report

机译:主动脉 - 肺窗,婴幼儿未识别的心力衰竭原因:案例报告

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Introduction : The aorto-pulmonary window is a rare congenital heart disease. It is a defect between the ascending aorta and the trunk of the pulmonary artery upstream of the pulmonary bifurcation. Once the diagnosis is made, surgery must be performed quickly to avoid progression to pulmonary arteriolitis. We report the case of a 4-month-old infant in whom we made the diagnosis of aorto-pulmonary window type I. He was able to benefit from an open heart surgery at FES with an excellent result after closing the window. Conclusion : The aorto-pulmonary window is a rare congenital heart defect, the diagnosis of which must be made as early as possible in order to avoid the progression to pulmonary hypetension and heart failure.
机译:简介:主动脉肺窗是一种罕见的先天性心脏病。它是肺部分叉上游肺动脉的升序与肺动脉的躯干之间的缺陷。一旦进行了诊断,必须快速进行手术以避免进展到肺动脉炎。我们举报了一个4个月大的婴儿,我们诊断了主动脉曲线窗口的诊断I.他能够在关闭窗户后的出色结果中受益于FES的开放性心脏手术。 结论:主动脉肺窗是一种罕见的先天性心脏缺损,其诊断必须尽早制作,以避免肺脓性和心力衰竭的进展。

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