Çocukluk çağı semptomatik aberran sağ subkavyan arter: Bir olgu sunumu

Purpose: The abberant right subclavian artery, in the existance of left archus aorta, is a common congenital aortic anomaly and has been reported to occur in 0.7% of the population in large autopsy series. However, if the aberrant right subclavian artery does not take place in a vascular ring formation, it is rarely symptomatic at the childhood period. Case report: A fourteen-months-old boy was attempted to the hospital with the complaints of wheezing; difficulty in breathing and failure of thrive. Chest X-ray, Magnetic resonance imaging and angiographies were performed and it was determined that symptoms were resulted from aberrant right subclavian artery. Conclusion: The case underwent a left posteriolateral thoracotomy; the aberrant right subclavian artery was resected from the archus aorta and anastomosis was done to the ascendant aorta. The post-operative period