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"Heart Sign" with Double Aortic Arch
Michael Scott Binder1, David Majdalany1
1Mayo Clinic, Rochester, NY 55901, USA.
Diagnostics (Basel, Switzerland)
|July 28, 2026
Summary
Double aortic arches are rare congenital vascular malformations. Surgical resection of the nondominant arch is typically recommended to alleviate symptoms caused by vascular rings.
Area of Science:
- Cardiology
- Congenital Malformations
- Vascular Surgery
Background:
- Double aortic arches are rare congenital malformations.
- Persistence of both right and left aortic arches leads to vascular rings.
- These rings can compress the trachea and esophagus, causing dysphagia and respiratory issues.
Purpose of the Study:
- To summarize the presentation and management of double aortic arches.
- To highlight the surgical approach for symptomatic patients.
Main Methods:
- Review of congenital vascular malformation cases.
- Description of surgical resection techniques for double aortic arches.
- Intraoperative monitoring of carotid and subclavian arteries.
Main Results:
- Double aortic arches can present in childhood or adulthood.
- Surgical resection of the nondominant arch effectively releases the vascular ring.
- Intraoperative monitoring ensures adequate distal perfusion post-surgery.
Conclusions:
- Double aortic arches are a treatable cause of dysphagia and respiratory distress.
- Surgical intervention is the standard treatment for symptomatic individuals.
- Careful surgical planning and monitoring are crucial for successful outcomes.
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