How Could Aortic Atresia With Interrupted Aortic Arch Survive? About a Neonatal Repair on Two Ventricles

被引:4
|
作者
Lacour-Gayet, Francois [1 ]
Kandachar, Pranav [1 ]
Al-Bulushi, Abdullah [2 ]
Maddali, Madan M. [1 ]
机构
[1] Royal Hosp, Natl Heart Ctr, Dept Cardiothorac Surg, Muscat, Oman
[2] Royal Hosp, Natl Heart Ctr, Dept Pediat Cardiol, Muscat, Oman
关键词
SEPTAL-DEFECT;
D O I
10.1053/j.semtcvs.2018.07.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aortic atresia with interrupted aortic arch (IAA) is an exceptional condition. In absence of associated lesion, the flow to the brain and the retrograde flow to the coronary arteries can only come from vessels on the descending aorta. This flow needs to be large enough to supply the brain and the myocardium. The only IAA type compatible with survival is type C where the flow from descending aorta could be insured by the left carotid and the left vertebral artery, branch of the left subclavian artery. Only one such a case was described in the literature. All the other surviving cases had an associated lesion including: a double aortic arch, an aorto-pulmonary window (AP window), an aberrant right subclavian artery or a bilateral patent ductus arteriosus (PDA). We report a case of aortic atresia with IAA type B associated with a double aortic arch that underwent a successful bi-ventricular one-stage neonatal Norwood-Rastelli repair and is doing well after 18 months. © 2018 Elsevier Inc.
引用
收藏
页码:118 / 121
页数:4
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