High Risk Features of an Anomalous Origin of the Right Coronary Artery
Dre Eleonore Campiche1, Jean-Paul Vallée2, David Carballo1
1Cardiology Department, University Hospitals of Geneva, 1205 Geneva, Switzerland.
Insights
Anomalous aortic origin of the coronary arteries (AAOCA) is a rare congenital heart defect. This case highlights a high-risk AAOCA presenting with sudden cardiac death symptoms, successfully treated with bypass surgery.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Cardiac Surgery
Background:
- Anomalous aortic origin of the coronary arteries (AAOCA) is a rare congenital abnormality.
- It is often asymptomatic, found incidentally, but can cause sudden cardiac death (SCD), especially in young athletes.
- AAOCA is the second most common cause of SCD in young athletes.
Observation:
- A 39-year-old patient presented with life-threatening symptoms suggestive of SCD.
- Initial diagnostics including ECG, echocardiography, and cardiac markers were normal.
- Coronary CT revealed a left-sided right coronary anomaly with hypoplasic origin and high-risk course between the aorta and pulmonary artery.
Findings:
- The anomalous coronary artery originated from the left sinus of Valsalva.
- It had a hypoplastic origin and a dangerous intramural path.
- The patient exhibited multiple high-risk features for SCD.
Implications:
- This case underscores the importance of advanced imaging like coronary CT in diagnosing high-risk AAOCA.
- Surgical management, such as coronary artery bypass, can be effective in preventing SCD in symptomatic patients.
- Early identification and intervention are crucial for patients with symptomatic AAOCA.
Abstract:
Anomalous aortic origin of the coronary arteries (AAOCA) is a rare congenital abnormality. It is usually asymptomatic and often found incidentally during coronary angiography. However, it can also be discovered during the autopsy of young healthy adults who have suffered from sudden cardiac death (SCD). AAOCA represents the second most common cause of SCD in young athletes. Herein, we report a case of a 39-year-old patient with left-sided right coronary anomaly with multiple high-risk features who presented with life-threatening symptoms for SCD but normal electrocardiography, echocardiography, and cardiac markers. The coronary computed tomography revealed an anomalous coronary artery from the left sinus of Valsalva with a hypoplasic origin and a high-risk path between the aorta and the pulmonary artery with a short intramural path. He was surgically managed with a coronary artery bypass with an uneventful follow-up.
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