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A History of Kawasaki Disease From Childhood and Coronary Artery Ectasia With Recurrent ST Elevation Myocardial Infarction: A Therapeutic Challenge

机译:小儿和冠状动脉蜕膜炎合并ST段抬高心肌梗死的川崎病史:治疗上的挑战

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摘要

Coronary artery ectasia (CAE) is an uncommon anomaly, usually found in 1.2-2% of patients undergoing coronary angiography, defined as a segment of the coronary artery that has a diameter of more than 1.5 times the normal adjacent segments. Atherosclerosis is considered as the cause of half of the CAE cases. We herein present a 65-year-old Asian male with past medical history of Kawasaki disease (KD) who developed recurrent episodes of inferior wall ST-elevation myocardial infarction (STEMI) despite treatment with dual antiplatelet therapy (DAPT). Repeat coronary angiogram showed severely ectatic and tortuous coronary arteries more predominant on the right coronary artery (RCA) with diffuse thrombus in its mid segment. Given his unfavorable vascular anatomy, the condition was managed medically with the addition of warfarin to his DAPT with target international normalized ratio (INR) 2 - 3. This case highlights the association of CAE with a prior history of KD and its therapeutic challenge.
机译:冠状动脉扩张(CAE)是一种罕见的异常,通常在进行冠状动脉造影的患者中占1.2-2%,定义为冠状动脉的一个部分,其直径超过正常相邻部分的1.5倍。动脉粥样硬化被认为​​是一半的CAE病例的原因。我们在此介绍了一位65岁的亚洲男性,具有川崎病(KD)的既往病史,尽管接受了双重抗血小板治疗(DAPT)治疗,但其复发性下壁ST抬高型心肌梗死(STEMI)发作。重复冠状动脉造影显示,右冠状动脉(RCA)上主要存在严重的直肠和曲折冠状动脉,中段弥漫性血栓。由于他的血管解剖结构不利,因此在医学上通过在他的DAPT中加入华法林(目标国际归一化比率(INR)2-3)来治疗该病。该病例强调了CAE与KD既往病史及其治疗挑战的关联。

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