A case of right sided aortic arch combined with atrial septal defect
Geun Jin Ha1, Myeung Joon Sung, Young Soo Lee
1Department of Cardiology, Catholic University of Daegu School of Medicine, Daegu, Korea.
Insights
Right-sided aortic arch, a rare congenital condition, can coexist with heart defects. This case highlights successful surgical repair in an 18-year-old female with an atrial septal defect and associated conditions.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Vascular Anomalies
Background:
- Right-sided aortic arch (RSAA) is a rare congenital anomaly with varied classifications based on aortic arch degeneration and great vessel branching.
- RSAA can be associated with significant congenital heart disease, with prevalence and type dependent on the specific RSAA classification.
- Understanding these associations is crucial for diagnosis and management.
Observation:
- A case report of an 18-year-old female presenting with a right-sided aortic arch.
- The patient exhibited an aberrant left subclavian artery, an atrial septal defect (ASD) of the ostium secundum type, moderate tricuspid regurgitation, and pulmonary hypertension.
- These findings represent a complex constellation of cardiovascular anomalies.
Findings:
- The patient's right-sided aortic arch was associated with an atrial septal defect (ostium secundum) and moderate tricuspid regurgitation.
- Pulmonary hypertension was noted, indicating significant hemodynamic impact.
- Surgical intervention involved successful patch closure of the ASD and tricuspid valve annuloplasty.
Implications:
- This case underscores the importance of recognizing the potential for associated cardiac defects in patients with right-sided aortic arch.
- Timely diagnosis and surgical correction of congenital heart disease, such as ASD, in the context of RSAA can lead to favorable outcomes.
- The successful management highlights the efficacy of surgical repair in improving patient prognosis.
Abstract:
Right sided aortic arch is an uncommon congenital anomaly. It can be classified into three types, depending on the left aortic arch's degenerating pattern and the branching pattern of the great vessels. It can be associated with major congenital heart disease, depending on the type of right sided aortic arch. We report a case of an 18-years-old female who has right sided aortic arch with atrial septal defect (ASD). In our case, the patient had a right sided aortic arch and aberrant left subclavian artery, also she had ASD (ostium secundum) and moderate tricuspid regurgitation with pulmonary hypertension. The patient was successfully performed patch closure of ASD and tricuspid valve annuloplasty via midline sternotomy. The patient had uneventful postoperative course.
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