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Shadowed Horizons: The Congenital Crisis of Aortic Arch Discontinuity
Jiao Peng1,2, Jie Wang3, Xiaojing Ma1
1Department of Ultrasound, Wuhan Asia Heart Hospital Affiliated to Wuhan University of Science and Technology, Wuhan Clinical Medical Research Center of Cardiovascular Imaging, Wuhan, China.
Insights
A rare case of dual ductal-dependent systemic perfusion in type C interrupted aortic arch highlights the need for early prenatal diagnosis. Timely intervention is crucial for managing this critical congenital heart defect.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Interrupted aortic arch is a severe congenital heart defect.
- Type C interrupted aortic arch presents unique challenges in systemic perfusion.
- Ductal-dependent systemic perfusion is a critical physiological state in neonates.
Abstract:
We report a rare case of dual ductal-dependent systemic perfusion in type C interrupted aortic arch. Despite imaging confirmation, ductal closure led to cardiopulmonary failure, and surgery was declined. This case underscores the critical need for prenatal diagnosis and coordinated perinatal management to enable timely intervention.
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