Type B Interrupted Left Aortic Arch with Isolated Right Subclavian Artery

被引：5
|
作者：
Knudson, Jarrod D. [1 ]
Lopez, Keila N. [1 ]
Maskatia, Shiraz [1 ]
McKenzie, Emmett D. [2 ]
Lantin-Hermoso, M. Regina [1 ]
Masand, Prakash M. [3 ]
Vick, Giles W., III [1 ]
机构：
[1] Texas Childrens Hosp, Baylor Coll Med, Dept Pediat, Div Pediat Cardiol, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Baylor Coll Med, Div Congenital Heart Surg, Dept Surg, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Baylor Coll Med, Dept Pediat Radiol, Houston, TX 77030 USA
来源：
CONGENITAL HEART DISEASE | 2012年 / 7卷 / 03期
关键词：
Interrupted Aortic Arch; Isolation of the Subclavian Artery; DiGeorge Syndrome; RIGHT PULMONARY-ARTERY; CARDIOVASCULAR ANOMALIES; ORIGIN; TRANSPOSITION;
D O I：
10.1111/j.1747-0803.2011.00625.x
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Interrupted aortic arch is a rare congenital heart malformation occurring in approximately three per 1 million births. Type B interrupted aortic arch (interruption between the second carotid artery and the ipsilateral subclavian artery) is the most common of three major types (A, B, and C). We report an extremely rare finding: a case of left-sided type B interrupted aortic arch with isolation of the right subclavian artery (origin from the right pulmonary artery).
引用
收藏
页码：E25 / E30
页数：6
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