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Published on: October 28, 2020
Quadricuspid aortic valve visualized by three-dimensional transthoracic echocardiography
Eser Acar1, Tayfun Sahin1, Irem Yılmaz1
1Department of Cardiology, School of Medicine, Kocaeli University, 41380 Kocaeli, Turkey.
A rare quadricuspid aortic valve, a congenital heart defect, can lead to aortic regurgitation. This case highlights its diagnosis in a patient presenting with angina pectoris using advanced echocardiography.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Medical Imaging
Background:
- Quadricuspid aortic valve (QAV) is a rare congenital anomaly.
- It can lead to significant cardiovascular complications, including aortic regurgitation.
- Early diagnosis is crucial for effective management.
Observation:
- A 77-year-old male presented with symptoms of stable angina pectoris.
- The patient was referred for further cardiac evaluation.
- Clinical presentation suggested potential underlying cardiac pathology.
Findings:
- Three-dimensional transthoracic echocardiography revealed a quadricuspid aortic valve.
- The imaging modality provided detailed anatomical visualization.
- The diagnosis of QAV was confirmed.
Implications:
- This case underscores the importance of considering rare congenital anomalies in adult patients with cardiac symptoms.
- Advanced echocardiography techniques are vital for accurate diagnosis of complex valve abnormalities.
- Understanding QAV is essential for appropriate clinical management and patient outcomes.
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