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Myocardial Infarction and Functional Outcome Assessment in Pigs
Published on: April 25, 2014
Double right coronary artery with acute inferior wall myocardial infarction
Manojkumar Rohit1, Shivkumar Bagga, Kewal Krishan Talwar
1Department of Cardiology, Post Graduate Institute of Medical Education and Research, Chandigarh 160012, India. manoj_786@hotmail.com
Insights
A rare double right coronary artery variation originating from one opening was identified. This anomaly led to a heart attack, successfully treated with angioplasty.
Area of Science:
- Cardiology
- Anatomical Variations
- Interventional Cardiology
Background:
- Coronary artery anomalies are uncommon but can lead to significant cardiovascular events.
- A double right coronary artery (DRCA) originating from a single ostium is exceptionally rare.
Observation:
- We present the first reported case of inferior wall myocardial infarction (MI) caused by occlusion in a DRCA.
- The anomaly involved a single ostium in the right sinus of Valsalva with two distinct right coronary arteries.
- A diagnostic challenge was presented by a high takeoff of a large right ventricular branch.
Findings:
- Successful management of the myocardial infarction was achieved using percutaneous coronary intervention (PCI).
- Angiographic diagnosis confirmed the rare DRCA anomaly and its occlusive pathology.
Implications:
- This case highlights the importance of recognizing rare coronary anomalies in the diagnosis and treatment of myocardial infarction.
- Understanding such variations is crucial for interventional cardiologists to ensure optimal patient outcomes.
- The findings emphasize the need for careful angiographic assessment to avoid misdiagnosis of coronary artery origins.
Abstract:
A double right coronary artery arising from a single ostium in the right sinus of Valsalva is an extremely rare coronary artery variation. We report for the first time in the literature a case of inferior wall myocardial infarction due to a double right coronary artery occlusion that was successfully managed with percutaneous coronary intervention. The rarity of this unusual coronary artery anomaly, its angiographic diagnosis and an important diagnostic dilemma of a high takeoff of a large right ventricular branch are discussed here.
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