Rebuttal: aortic coarctation and concomitant anomalies - left circumflex fistula, persistent left SVC and ventricular
1Imaging Insititute, Cleveland Clinic Abu Dhabi, Abu Dhabi, Abu Dhabi, UAE.
Insights
Coarctation of the aorta (COA) is a common congenital heart defect. This case highlights a rare combination of COA with multiple cardiovascular anomalies, emphasizing the complexity of managing such conditions.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Medical Case Reports
Background:
- Coarctation of the aorta (COA) is a significant congenital cardiovascular anomaly affecting up to 6 per 1000 live births.
- Associated rare cardiovascular anomalies can complicate COA management.
- Hypertension in adolescents can be an indicator of underlying COA.
Purpose of the Study:
- To report a rare case of coarctation of the aorta in an adolescent male.
- To describe the incidental diagnosis of hypertension leading to COA detection.
- To document an unprecedented association of COA with specific rare anomalies.
Main Methods:
- Case presentation of an adolescent male with incidental hypertension.
- Diagnostic imaging to confirm coarctation of the aorta.
- Literature review to assess the novelty of associated anomalies.
Main Results:
- Coarctation of the aorta was confirmed via imaging.
- The patient presented with multiple, rarely associated cardiovascular anomalies.
- The specific combination of COA with left circumflex to coronary sinus fistula, ventricular diverticulum, and persistent left superior vena cava appears to be previously unreported.
Conclusions:
- This case underscores the importance of investigating hypertension in adolescents.
- The co-occurrence of COA with these specific anomalies presents a unique clinical scenario.
- Further research may be needed to understand the implications of such complex congenital heart defect associations.
Abstract:
Coarctation of the aorta (COA) is a relatively common cardiovascular congenital anomaly. It can be seen in up to 6 per 1000 live births. Rare cardiovascular anomalies have been found to be associated with COA, which may complicate management. We present a case of an adolescent male, incidentally found to be hypertensive. COA was confirmed on imaging, however, with multiple anomalies with an incidence in the general population as common as 0.4 per cent to as rare as 7 cases ever reported in the literature. The association of COA with left circumflex to coronary sinus fistula, ventricular diverticulum and persistent left superior vena cava has never been reported to our knowledge.
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