RIGHT AORTIC-ARCH WITH ABERRANT RETROESOPHAGEAL INNOMINATE-ARTERY - A REPORT OF 2 CASES AND REVIEW OF THE LITERATURE

被引:11
作者
NAKAJIMA, Y
SATOMI, G
KAWAMURA, T
NISHIBATAKE, M
NAKAZAWA, M
TAKAO, A
机构
[1] Department of Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical College 8-1, Shinjuku-ku, Tokyo, 162, Kawada-cho
关键词
RETROESOPHAGEAL INNOMINATE ARTERY; AORTIC ARCH ANOMALY; PATHOGENESIS;
D O I
10.1016/0167-5273(93)90242-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We describe two patients of right aortic arch associated with aberrant retroesophageal innominate artery. One case was associated with tetralogy of Fallot and a tortuous left common carotid artery originating from the retroesophageal innominate artery. Tetralogy of Fallot associated with this kind of aortic arch anomaly has never before been reported. The other case was associated with a perimembranous ventricular septal defect. Symptoms such as dyspnea, dysphagia and recurrent respiratory infection due to the compression by the vascular anomaly were not noted in these two cases. The morphological findings are indicative of a double aortic arch with an interruption of the left arch proximal to the common carotid artery.
引用
收藏
页码:247 / 251
页数:5
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