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ARTICLE | October 1969

Congenital Aortic Vascular Ring

Bernard L. Tucker, MD; Bert W. Meyer, MD; George G. Lindesmith, MD; Quentin R. Stiles, MD; John C. Jones, MD

Arch Surg. 1969;99(4):521-523. doi:10.1001/archsurg.1969.01340160101023.

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Compression of the trachea and esophagus by vascular anomalies of the aortic arch and its branches may be a threat to life in infancy. The significance of the so-called vascular ring, long recognized as a cause of obstruction of the trachea and esophagus in early life, assumed new importance in 1945 when the operation by Gross¹ placed this entity among the surgically correctable congenital lesions of the great vessels. Since that time, experience with the operative treatment of these anomalies has been accumulated.^2-4

In the normal 12-mm human embryo, the aortic trunk divides into a left and a right arch. These arches pass on either side of the trachea and esophagus and rejoin to form a single descending dorsal aorta. Normally, a process of absorption or resolution takes place in the right arch distal to the right subclavian, leaving the remaining portion of the right arch to become

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Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

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Tucker BL, Meyer BW, Lindesmith GG, Stiles QR, Jones JC. Congenital Aortic Vascular Ring. Arch Surg. 1969;99(4):521-523. doi:10.1001/archsurg.1969.01340160101023.

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