Right Aortic Arch with a Retroesophageal Left Subclavian Artery and an Anomalous Origin of the Pulmonary Artery from the Aorta.
10.5090/kjtcs.2017.50.1.44
- Author:
Chang Seok JEON
1
;
Man shik SHIM
;
Ji Hyuk YANG
;
Tae Gook JUN
Author Information
1. Department of Thoracic and Cardiovascular Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Korea. tgjunsmc@gmail.com
- Publication Type:Case Report
- Keywords:
Congenital heart disease;
Aortic arch;
DiGeorge syndrome
- MeSH:
Anatomic Variation;
Aorta*;
Aorta, Thoracic*;
DiGeorge Syndrome;
Echocardiography;
Heart Defects, Congenital;
Humans;
Infant, Newborn;
Pulmonary Artery*;
Subclavian Artery*
- From:The Korean Journal of Thoracic and Cardiovascular Surgery
2017;50(1):44-46
- CountryRepublic of Korea
- Language:English
-
Abstract:
We report the case of a newborn with a rare anatomic variation: a right aortic arch with a retroesophageal left subclavian artery and an anomalous origin of the pulmonary artery from the aorta. This variation was diagnosed using echocardiography and computed tomography, and we treated the condition surgically.