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Published on: September 13, 2020
Aberrant right subclavian artery intervention can provide relief of dysphagia
Cathlyn K Medina1, John A Kucera1, Berk Aykut1
1Congenital Heart Surgery Research and Training Laboratory, Duke University, Durham, NC, USA.
Insights
Aberrant right subclavian artery (ARSA) can rarely cause severe dysphagia in children. Surgical correction through subclavian reimplantation effectively resolved swallowing difficulties and improved weight gain in a small patient cohort.
Area of Science:
- Cardiovascular Surgery
- Pediatric Surgery
- Vascular Anomalies
Background:
- Aberrant right subclavian artery (ARSA) is the most common aortic arch vascular anomaly.
- Traditionally, ARSA is not considered a cause of dysphagia.
- This study challenges conventional wisdom by presenting cases where ARSA caused significant swallowing issues.
Purpose of the Study:
- To investigate the potential link between ARSA and dysphagia in pediatric patients.
- To present a series of cases where ARSA was the cause of debilitating dysphagia.
- To evaluate the efficacy of surgical intervention for ARSA-induced dysphagia.
Main Methods:
- A cohort of four children with dysphagia attributed to ARSA was studied.
- Surgical intervention involved subclavian reimplantation.
- The surgical approach utilized was a right posterolateral thoracotomy.
Main Results:
- All four patients experienced complete resolution of dysphagia postoperatively.
- Patients were able to transition to a normal diet and achieve appropriate weight gain.
- Clinical follow-up indicated sustained positive outcomes.
Conclusions:
- ARSA should be considered a rare but potential cause of dysphagia in children.
- Surgical management, specifically subclavian reimplantation, can lead to dramatic symptom resolution.
- This case series highlights the importance of considering ARSA in the differential diagnosis of pediatric dysphagia.
Background:
An aberrant right subclavian artery represents the most common aortic arch vascular anomaly. Conventional wisdom states that these anomalies do not result in dysphagia, but rather serve as "red herrings". Clearly, in the vast majority of cases, this holds true. Nonetheless, one should never say never.
Methods:
Herein, we present a cohort of four children with debilitating dysphagia resulting from an aberrant right subclavian artery. Subclavian reimplantation via a right posterolateral thoracotomy was performed successfully in all cases.
Results:
Dysphagia resolved postoperatively, and all patients were able to advance to a normal diet. They were able to gain appropriate weight postoperatively and continue to do well at most recent clinical follow-up.
Conclusions:
This case series suggests that aberrant right subclavian artery anatomy should be considered a potential aetiology of dysphagia, albeit rarely. Surgical intervention for select patients can provide dramatic resolution of symptoms.
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