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A functioning double aortic arch in an infant: a case report

F Machiels1, M de Maeseneer, B Desprechins

  • 1Department of Pediatric Radiology, Academic Hospital, Free University of Brussels, Belgium.

Pediatric Radiology
|January 1, 1994
PubMed
Summary
This summary is machine-generated.

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A rare double aortic arch in an infant caused breathing issues and feeding difficulties. Imaging revealed typical findings of this congenital vascular anomaly.

Area of Science:

  • Cardiology
  • Pediatric Surgery
  • Medical Imaging

Background:

  • Congenital vascular anomalies, such as a double aortic arch, are rare but can cause significant clinical symptoms in infants.
  • Early diagnosis and characterization of vascular rings are crucial for timely intervention.

Observation:

  • A 4-month-old boy presented with recurrent respiratory infections and poor feeding, suggestive of an underlying structural abnormality.
  • Diagnostic imaging modalities including esophagogram, Doppler echocardiography, and aortography were employed.

Findings:

  • The diagnostic workup confirmed a functioning double aortic arch, a rare congenital condition.
  • The study details the characteristic imaging findings associated with this specific vascular anomaly.

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Implications:

  • Accurate identification of a double aortic arch through imaging is essential for pediatricians and surgeons.
  • Understanding the typical presentation aids in the prompt diagnosis and management of symptomatic infants with this rare disorder.