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Early Detection of Anomalous Origin of Left Coronary Artery from the Right Pulmonary Artery After Successful Repair of Critical Coarctation of the Aorta

机译:成功修复主动脉缩窄后,从右肺动脉早期发现左冠状动脉异常起源

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摘要

Left ventricular (LV) function is impaired by increased afterload in neonates with severe coarctation of the aorta, which may result in endocardial fibroelastosis. Repair of the coarctation usually solves the problem, with LV function normalizing after a few weeks. This report describes a patient who underwent successful repair of critical coarctation with normalization of LV function despite signs of endocardial fibroelastosis but with persisting elevation of cardiac troponin T. Cardiac catheterization showed the rare coincidence of anomalous origin of left coronary artery from the right pulmonary artery (ALCAPA) and coronary sinus orifice atresia with left superior vena cava. Keywords ALCAPA - Cardiac troponin T - Coarctation of the aorta - Coronary sinus orifice atresia
机译:新生儿后负荷增加,主动脉严重缩窄会损害左心室(LV)功能,这可能导致心内膜纤维弹性。缩窄的修复通常可以解决问题,几周后LV功能恢复正常。本报告描述了一名患者,尽管有心内膜纤维弹性增生的迹象,但心脏功能肌钙蛋白T持续升高,但LV功能正常化但仍成功修复了严重的缩窄症。 ALCAPA)和冠状窦口闭锁伴左上腔静脉。关键词ALCAPA-心肌肌钙蛋白T-主动脉缩窄-冠状窦口闭锁

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