Anomalous origin of left pulmonary artery branch from the aorta with Fallot's tetralogy:one case report

我们报导经常与呼吸窘迫介绍了的一个十岁的男孩的案例后来出生。胸 X 光检查显示出一个扩大右室。Echocardiography 证明 Fallot 的四联剧和左肺的动脉的典型特征不能被设想。然而，心导管插入术透露左肺的动脉在上升主动脉有异常起源。病人经历了缺点的全部的外科的修正。九天以后，他被解除。我们在场发生的文学评论的结果， physiopathological，这稀罕疾病的临床、诊断、外科的特征。

We report the case of a ten-year-old boy who had often presented with respiratory distress since born. Chest X-ray showed an enlarged right ventricle. Echocardiography demonstrated characteristic features of Fallot＇s tetralogy and the left pulmonary artery could not be visualized. However, cardiac catheterization disclosed that the left pulmonary artery had an anomalous origin in the ascending aorta. The patient underwent total surgical correction of the defects. Nine days later, he was discharged. We present the results of a literature review of the incidence, physiopathological, clinical, diagnostic, and surgical characteristics of this rare disease.