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.

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