Double left anterior descending coronary artery originating from left main coronary stem and right coronary artery
Fariborz Akbarzadeh1, Sepide Shadravan, Maryam Ghorbanian
1Cardiovascular Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Insights
A rare congenital heart anomaly, double left anterior descending coronary artery, was observed. One artery originated normally, while the second arose from the right coronary artery, a unique presentation.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Anatomical Variations
Background:
- Congenital coronary artery anomalies are uncommon, impacting cardiac function and surgical planning.
- The double left anterior descending coronary artery (LAD) is a rare variant, with varying origins reported.
- Understanding these anomalies is crucial for accurate diagnosis and treatment.
Observation:
- A case report details a patient with a double left anterior descending coronary artery.
- One LAD exhibited a typical origin from the left main coronary stem.
- The second LAD anomalously originated from the right coronary artery.
Findings:
- This case presents a unique anatomical variation of the coronary arteries.
- The coexistence of a normally originating LAD and an LAD from the right coronary artery is exceptionally rare.
- Documentation of such cases contributes to the limited existing literature.
Implications:
- Accurate identification of coronary anomalies is vital for preventing potential complications like myocardial infarction.
- This case highlights the importance of detailed coronary imaging in cardiovascular diagnostics.
- Further research into the embryological basis and clinical significance of such anomalies is warranted.
Abstract:
Double left anterior descending coronary artery originating from left main coronary stem and right coronary artery is a rare congenital coronary anomaly. In this case report, we are describing a patient with double left anterior descending coronary artery, one with normal origin, and the other originating from the right coronary artery. To the best of our knowledge, there are only a few reports resembling such case.
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