Coronary arterial spasm in single right coronary artery

En-zhi Jia1, Qi-jun Shan, Zhi-jian Yang

  • 1Department of Cardiovascular Medicine, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China. enzhijia@yahoo.cn

Insights

A rare single right coronary artery anomaly was found in a syncope patient. Treatment for coronary artery spasm prevented further fainting episodes.

Area of Science:

  • Cardiology
  • Radiology
  • Medical Imaging

Background:

  • Coronary artery anomalies are rare congenital conditions that can predispose individuals to various cardiovascular issues.
  • Syncope, or fainting, can be a symptom of underlying cardiac pathology, including coronary artery abnormalities.
  • Advanced imaging techniques like dual-source computed tomography (DSCT) angiography are crucial for diagnosing complex coronary artery variations.

Observation:

  • A 32-year-old male presented with recurrent syncope and pre-syncope.
  • Coronary angiography and DSCT angiography revealed an anomalous single right coronary artery.
  • A significant branch arose from the proximal single right coronary artery, coursed anterior to the pulmonary artery, and bifurcated into the left anterior descending and circumflex arteries.

Findings:

  • The patient exhibited a rare single coronary artery originating as a large right coronary artery.
  • The anomalous vessel supplied territory typically supplied by the left coronary system.
  • Syncope episodes were attributed to potential coronary artery spasm.

Implications:

  • This case highlights the importance of recognizing rare coronary artery anomalies during routine investigations.
  • Early diagnosis and appropriate management, such as anti-spasmodic medication (diltiazem), can effectively treat symptoms like syncope associated with coronary anomalies.
  • DSCT angiography is a valuable tool for delineating complex coronary artery anatomy and guiding clinical management.

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