Case Report and Literature Review of an Anomalous Course of the Left Main Coronary Artery (LMCA) Arising From the Right Sinus of Valsalva (RSV) Presenting as Takotsubo Cardiomyopathy

被引:0
|
作者
Gaddameedi, Sai Rakshith [1 ]
Thapa, Milan [1 ]
Arty, Fnu [1 ]
Atreya, Suryansh [1 ]
Ravilla, Jayasree
Panchal, Pratik [2 ]
Du, Doantrang [1 ]
机构
[1] Rutgers Hlth Monmouth Med Ctr, Internal Med, Long Branch, NJ 07740 USA
[2] Rutgers Hlth Monmouth Med Ctr, Cardiol, Long Branch, NJ USA
关键词
coronary artery anomaly (caa); takotsubo-like cardiomyopathy; takotsubo cardiomyopathy; left circumflex artery; left main coronary artery; right sinus of valsalva; left coronary artery anomaly; congenital coronary artery anomaly; embryological coronary artery anomaly;
D O I
10.7759/cureus.63028
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Takotsubo cardiomyopathy (TC) mimics myocardial infarction with symptoms like chest pain, electrocardiogram (EKG) changes, and elevated troponin levels, although it typically features normal coronary arteries upon angiography. While often asymptomatic, coronary artery anomalies (CAAs) can cause intermittent vasospasm and endothelial dysfunction, potentially inducing TC. We report the case of a 74year-old female with a history of hypertension, hyperlipidemia, and peripheral artery disease, who presented with sudden onset chest pain. Initial EKG and elevated troponin suggested myocardial infarction. However, coronary angiography revealed an anomalous left main coronary artery (LMCA) originating from the right coronary artery (RCA), with no significant stenosis. Subsequent transthoracic echocardiography indicated TC, with the left ventricular ejection fraction improving from 35-40% to 60-65% within days. Cardiac computed tomography angiography (CCTA) revealed that the anomalous LMCA originated from the common trunk at the right sinus of Valsalva (RSV), which further continued as a large, dominant RCA. The LMCA branched into a small to moderate left anterior descending artery (LAD) and a non -dominant left circumflex artery (LCx). The LMCA followed a prepulmonic/anterior course, while the LCx took an interarterial course between the aorta and pulmonary artery. The patient was referred for further surgical evaluation. We conclude that the CAA was an incidental finding and was not related to underlying TC. Although rare, this case suggests a possible correlation between CAAs and a predisposition to stress-induced cardiomyopathy, warranting further investigation.
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