Coronary Artery Anomalies: A Short Case Series and Current Review
Md Mashiul Alam1, Tasniem Tasha2, Ammy S Ghosh3
1Internal Medicine, Bridgeport Hospital/Yale University, Bridgeport, USA.
Insights
Coronary artery anomalies (CAAs), rare congenital heart defects, can cause serious issues including sudden cardiac death (SCD) in athletes. This study reviews CAA cases, diagnostic methods, and treatments for better patient management.
Area of Science:
- Cardiology
- Congenital Cardiovascular Defects
Background:
- Coronary artery anomalies (CAAs) are uncommon congenital cardiovascular defects.
- Their presentation varies based on the abnormal coronary artery fistula's origin, course, and termination.
- CAAs are often incidentally discovered during coronary angiography or autopsies.
Observation:
- While many adults with CAAs are asymptomatic, some may develop symptoms like angina, heart failure, myocardial infarction, cardiomyopathy, or ventricular aneurysms.
- Coronary artery anomalies are the second leading cause of sudden cardiac death (SCD) in young athletes.
- This series presents five illustrative cases of CAAs, highlighting diverse clinical manifestations.
Findings:
- The study reviews various types of coronary artery anomalies.
- It discusses current diagnostic tools and therapeutic strategies for managing CAAs.
- Case examples demonstrate the wide spectrum of CAA presentations and potential complications.
Implications:
- Increased awareness and further research are crucial for efficient management of patients with CAAs.
- Understanding the varied presentations of CAAs can improve early diagnosis and intervention.
- This review provides valuable insights for clinicians dealing with rare congenital coronary artery anomalies.
Abstract:
Coronary artery anomalies (CAAs) are rare congenital cardiovascular defects that can present in various ways depending on the origin, course, and termination of the abnormal coronary artery fistula. It is sometimes detected incidentally during procedures such as coronary angiography or autopsies. While adults with this condition are often asymptomatic, some may experience angina, congestive heart failure, myocardial infarction, cardiomyopathy, ventricular aneurysms, or sudden cardiac death (SCD). In fact, it is the second leading cause of SCD among young athletes and requires more studies to handle such patients efficiently. To illustrate the many possible manifestations of this unusual diagnosis, we present a series of five cases. We have also reviewed the different varieties of this rare congenital anomaly and discussed the latest diagnostic tests and treatment plans.
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