Single coronary artery anomaly: a report of three cases
Alper Canbay1, Ozlem Ozcan, Sinan Aydoğdu
1Department of Cardiology, Ankara Numune Training and Research Hospital, Ankara, Turkey.
Insights
Anomalous single coronary artery, a rare congenital heart variation, can present with varied symptoms and requires careful diagnosis. This study highlights three cases, emphasizing the importance of coronary angiography in identifying this condition.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Diagnostic Imaging
Background:
- Congenital coronary artery anomalies are rare but can lead to significant cardiovascular events.
- A single coronary artery is a rare anomaly where the entire heart is supplied by one vessel.
- Incidental detection during routine procedures necessitates understanding of varied presentations.
Purpose of the Study:
- To present three distinct cases of anomalous single coronary artery.
- To illustrate the diagnostic approach and clinical implications of this anomaly.
- To discuss management strategies based on anatomical variations and patient symptoms.
Main Methods:
- Retrospective case series.
- Review of coronary angiography findings.
- Clinical correlation of symptoms and outcomes.
Main Results:
- Three patients with anomalous single coronary artery were identified during routine coronary angiography.
- Case 1: Type L-I anomaly with non-cardiac chest pain, resolved without intervention.
- Case 2: Type R-I anomaly with significant stenosis, successfully treated with bypass surgery.
- Case 3: Type R-II-B anomaly with high-risk anatomical course, surgery recommended but refused.
Conclusions:
- Anomalous single coronary artery can present with diverse clinical scenarios, from asymptomatic to requiring surgical intervention.
- Coronary angiography is crucial for diagnosing and characterizing single coronary artery anomalies.
- Management should be individualized based on the specific anomaly, associated pathologies, and patient presentation.
Abstract:
We presented three cases of anomalous single coronary artery detected incidentally during routine coronary angiography. The presenting symptoms were chest pain, angina pectoris, and exertional chest pain, respectively. In one case (male, 69 years), the single coronary artery gave off branches to the left anterior descending artery, left circumflex (LCx) artery, and right coronary artery (RCA) (type L-I). There were no atherosclerotic lesions. The patient's chest pain was thought to have a noncardiac origin and it did not recur during a 12-month follow-up. In another case (male, 65 years), the single coronary artery originated from the right sinus of Valsalva, and gave off branches to the RCA and the left coronary system (type R-I). The patient underwent coronary artery bypass surgery for significant stenotic lesions in the LCx and RCA. He was free of angina pectoris within 12 months after surgery. In the third case (female, 48 years), a single coronary ostium gave branches to the right and left coronary systems (type R-II-B). As the course of the coronary artery was between the aorta and pulmonary artery, surgery was recommended, but the patient refused surgery.
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