Rare Mechanism of Anterior Myocardial Infarction Secondary to Aortic Dissection

Q4 Medicine
Isa Khan MD , Kevin Rajakariar MBBS , Yuvaraj Malaiapan MBBS, MD
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引用次数: 0

Abstract

A 76-year-old woman presented with anterolateral ST-segment elevation myocardial infarction complicated by incessant ventricular arrhythmia. Angiography did not find obstructive coronary disease. Echocardiography demonstrated “double valve sign,” pathognomonic of aortic dissection, which was subsequently confirmed on computed tomography. The coronary arteries arose from the true lumen; thus, it was understood that her presentation was caused by external coronary ostia compression by the growing false aortic lumen. It has long been understood that when aortic dissection involves the coronary arteries, it typically affects the right artery. This case highlights a rare complication of aortic dissection affecting the left coronary artery.
主动脉夹层继发于前壁心肌梗死的罕见机制。
一位76岁女性,以st段前外侧抬高型心肌梗死合并不间断室性心律失常。血管造影未发现阻塞性冠状动脉疾病。超声心动图显示“双瓣征”,主动脉夹层的典型症状,随后在计算机断层扫描上证实。冠状动脉起源于真管腔;因此,可以理解的是,她的表现是由生长的假主动脉腔压迫冠状动脉外口引起的。人们早就知道,当主动脉夹层累及冠状动脉时,它通常会影响右动脉。这个病例强调了一个罕见的并发症主动脉夹层影响左冠状动脉。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JACC. Case reports
JACC. Case reports Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.30
自引率
0.00%
发文量
404
审稿时长
17 weeks
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