[Single coronary artery and right aortic arch]
Efrén Martínez-Quintana1, Fayna Rodríguez-González2
1Servicio de Cardiología, Complejo Hospitalario Universitario Insular-Materno Infantil, Las Palmas de Gran Canaria, España.
Insights
This case report highlights two rare coronary anomalies: a single coronary artery from the right sinus of Valsalva and a right aortic arch. These anomalies, though often asymptomatic, are crucial for diagnosing cardiac events in patients.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Vascular Anatomy
Background:
- Coronary artery anomalies are congenital variations in the origin or course of the coronary arteries.
- Most coronary anomalies are asymptomatic and discovered incidentally.
- However, they can be associated with significant cardiovascular events, including myocardial infarction and sudden cardiac death, particularly in younger individuals.
Observation:
- The study presents a rare case of a 65-year-old patient with concurrent rare coronary anomalies: a single coronary artery originating from the right sinus of Valsalva and a right aortic arch.
- The patient also had atherosclerotic coronary artery disease.
Findings:
- The coexistence of a single coronary artery from the right sinus of Valsalva and a right aortic arch is exceedingly rare.
- This combination of anomalies necessitates careful consideration in the differential diagnosis of various cardiac symptoms.
Implications:
- Recognition of these rare anomalies is critical for accurate diagnosis and management of patients presenting with angina, dyspnea, syncope, or myocardial infarction.
- This case underscores the importance of comprehensive cardiovascular assessment, especially when anatomical variations are suspected.
- Understanding these anomalies aids in preventing misdiagnosis and ensuring appropriate treatment strategies for affected individuals.
Abstract:
Coronary anomalies are mostly asymptomatic and diagnosed incidentally during coronary angiography or echocardiography. However, they must be taken into account in the differential diagnosis of angina, dyspnea, syncope, acute myocardial infarction or sudden death in young patients. The case is presented of two rare anomalies, single coronary artery originating from right sinus of Valsalva and right aortic arch, in a 65 year-old patient with atherosclerotic coronary artery disease treated percutaneously.
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