先天性冠状动脉扩张合并室间隔缺损一例罕见

T. Huang, W. Lu, K. Chien
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摘要

特发性或先天性冠状动脉扩张(CAE)是一种罕见的冠状动脉疾病。在成人中,冠状动脉扩张通常与动脉粥样硬化改变有关,是心导管插入术中常见的临床症状。小儿冠状动脉扩张通常与川崎病的后遗症有关。先天性冠状动脉扩张是罕见的,很少报道在儿童。我们提出一个病例的婴儿谁有冠状动脉扩张,她也有室间隔缺损(VSD)和心力衰竭谁接受了室间隔修复婴儿期。没有阻塞性冠状动脉疾病,也没有确定病变的原因。这些患者的预后和最佳治疗仍然未知。抗血小板治疗可能是必要的,以保持患者免于心肌缺血。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Occurrence of Congenital Coronary Ectasia Combined with Ventricular Septal Defect
Idiopathic or congenital coronary artery ectasia (CAE) is an uncommon form of coronary artery disease. In adults, coronary artery ectasia is usually associated with atherosclerotic change and is well recognized clinical entity encountered during cardiac catheterization. Coronary artery dilatation in pediatric is usually associated with the sequelae of Kawasaki disease. Congenital coronary artery ectasia is uncommon and rarely reported in children. We present a case of an infant who have dilated coronary artery, she also had ventricular septal defect (VSD) and heart failure who had received VSD repair at infancy. There was no obstructive coronary artery disease, and no cause for the lesions could be identified. The prognosis and optimal management of such patients remains unknown. Antiplatelet therapy might be necessary for the patient to remain free of myocardiac ischemia.
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