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Severe form of persistent thebesian veins presenting as ischemic heart disease
Younghee Jung1, Hyun-Jin Kim, Chang-Hwan Yoon
1Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Insights
Persistent Thebesian veins, a rare coronary artery anomaly, can cause myocardial ischemia. This case highlights the importance of recognizing these fistulae for effective patient management and treatment.
Area of Science:
- Cardiology
- Congenital Heart Disease
Background:
- Coronary artery fistula is a rare congenital anomaly.
- While often asymptomatic, it can lead to heart failure, myocardial ischemia, or arrhythmias.
Purpose of the Study:
- To report a case of myocardial ischemia caused by persistent Thebesian veins.
- To describe the diagnostic findings and management of this rare condition.
Main Methods:
- Case report presentation.
- Diagnostic coronary angiography to visualize the fistula and its drainage.
Main Results:
- The patient presented with myocardial ischemia.
- Coronary angiography revealed multiple microfistulae draining into the left ventricle via persistent Thebesian veins.
- The patient improved with medical management.
Conclusions:
- Persistent Thebesian veins can be a cause of myocardial ischemia.
- Medical management with beta-blockers and ACE inhibitors can be effective.
- Coronary angiography is crucial for diagnosis.
Abstract:
Coronary artery fistula is a rare congenital anomaly. Most patients with this anomaly are asymptomatic, but some may develop heart failure, myocardial ischemia or arrhythmias. We report a case of a patient who presented with myocardial ischemia secondary to persistent Thebesian veins. Coronary angiography demonstrated a marked capillary blush draining into the left ventricular cavity through multiple microfistulae from the left anterior descending artery, left circumflex artery and right coronary artery. The patient was discharged without chest pain and was medically maintained with a beta-blocker and angiotensin converting enzyme inhibitor.
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