Rees A H, Elbl F, Villafane J, Solinger R, Mavroudis C, Harrison H
Department of Pediatrics, University of Louisville, KY 40292.
J Ky Med Assoc. 1990 Feb;88(2):62-5.
A seven-week-old infant with multiple areas of coarctation of the abdominal aorta and renal artery pathology underwent staged surgical repair of his malformations in our medical center. The clinical and routine echocardiographic evaluations suggested the diagnosis of atypical coarctation of the aorta. The exact anatomical characteristics of his vascular malformations were established by repeated angiocardiographic studies, which should be performed in any patient in which the diagnosis of atypical coarctation of the aorta is suspected.
一名患有腹主动脉多处缩窄及肾动脉病变的7周龄婴儿在我们医疗中心接受了分期手术修复其畸形。临床及常规超声心动图评估提示为非典型主动脉缩窄。通过反复的心血管造影研究确定了其血管畸形的确切解剖特征，对于任何疑似非典型主动脉缩窄的患者均应进行此项检查。
