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Aortic arch uncrossing using a tracheal resection procedure
1Cardiac Surgery Division, Gaslini Children's Hospitals, Genova, Italy.
Multimedia Manual of Cardiothoracic Surgery : MMCTS
|June 22, 2021
Summary
A rare right aortic arch with Kommerell's diverticulum caused severe tracheal compression and tracheomalacia. Surgical repair involving tracheal resection and aortic arch translocation effectively relieved symptoms in a pediatric patient.
Area of Science:
- Cardiovascular Surgery
- Pediatric Surgery
- Thoracic Surgery
Background:
- Right aortic arch with Kommerell's diverticulum is a rare congenital anomaly causing vascular rings.
- These anomalies can lead to significant compression of the trachea and esophagus, resulting in respiratory and swallowing difficulties.
Observation:
- A 10-month-old patient presented with recurrent respiratory symptoms due to residual compression from a right aortic arch and Kommerell's diverticulum after initial surgery.
- CT scans and airway endoscopy revealed persistent tracheal compression and tracheomalacia in the affected segment.
Findings:
- Initial surgical intervention (anterior arch division and posterior aortopexy) provided only temporary relief.
- A second surgical procedure involving resection of the tracheomalacic trachea and anterior translocation of the aortic arch was performed.
Implications:
- This case highlights the complexity of managing symptomatic vascular rings, particularly those with associated tracheomalacia.
- Surgical translocation of the aortic arch anterior to the airway may be a viable option for relieving persistent compression and improving outcomes in select pediatric patients.
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