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Published on: August 18, 2016
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.
Abstract:
We presented a case of anomalous single-coronary artery detected incidentally during routine coronary angiography. A 32-year-old male Chinese patient presented with recurrent pre-syncope and six episodes of syncope. Coronary angiography and coronary-computed tomography (CT)-angiography performed by a dual-source computed tomography (DSCT) revealed that the patient had a single large right coronary artery. A moderately large branch originated from the proximal part of the single right coronary artery and extended to the left, passing the anterior to the pulmonary artery, and divided into the anterior descending artery branch and circumflex branch at the base of the left auricular appendage. The episodes of the syncope were suspected to be caused by coronary arterial spasm, so this patient was on a regimen of 30 mg of diltiazem every 6 h and had no recurrence of syncope during follow-up.
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