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Published on: March 14, 2017
Noninvasive imaging of isolated persistent fifth aortic arch
S-G Yang1, M A Fogel, P Stephens
1Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
A rare congenital heart defect, persistent fifth aortic arch, was identified in an infant using echocardiography and confirmed with magnetic resonance imaging (MRI). This case highlights a very uncommon anomaly in pediatric cardiology.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Medical Imaging
Background:
- Congenital heart defects represent a significant area of pediatric cardiovascular research.
- The persistent fifth aortic arch is an exceedingly rare congenital anomaly with limited documented cases.
- Accurate diagnosis of rare cardiac malformations is crucial for appropriate management.
Observation:
- Echocardiography initially suggested the presence of a persistent fifth aortic arch in an infant presenting with a heart murmur.
- Magnetic resonance imaging (MRI) provided definitive confirmation of this rare congenital anomaly.
- The infant's clinical presentation included a notable heart murmur, prompting diagnostic investigation.
Findings:
- The study successfully confirmed a diagnosis of persistent fifth aortic arch.
- Magnetic resonance imaging (MRI) was instrumental in visualizing and confirming the anomaly.
- Three-dimensional reconstructions from MRI data offered detailed anatomical insights.
Implications:
- This case contributes to the limited literature on persistent fifth aortic arch, enhancing understanding of its presentation.
- Advanced imaging techniques like MRI are vital for diagnosing rare and complex congenital heart diseases.
- Increased awareness of such rare anomalies can improve early detection and clinical management in infants.
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