Alva-Espinosa C, Jiménez-Arteaga S, Díaz-Díaz E, Martínez-Sanchez A, Jiménez-Zepeda D, Mojarro-Ríos J, Meléndez-López C
Department of Pediatric Echocardiography, Hospital de Cardiología, Centro Médico Nacional Siglo XXI, IMSS, D.F., Mexico City, México.
Pediatr Cardiol. 1995 Jan-Feb;16(1):42-4. doi: 10.1007/BF02310336.
A 6-month-old male infant with coexistent type B interrupted aortic arch, distal aortopulmonary window, and anomalous origin of the right pulmonary artery arising from the ascending aorta was diagnosed by two-dimensional echocardiography, color Doppler, and cardiac catheterization. Review of the available literature reveals this patient to be the fourteenth reported case of this unusual association of cardiovascular defects.
一名6个月大的男婴,合并B型主动脉弓中断、远端主肺动脉窗及右肺动脉起源于升主动脉异常,通过二维超声心动图、彩色多普勒及心导管检查得以确诊。查阅现有文献发现,该患者是这种不寻常心血管缺陷组合的第14例报告病例。