Vargas Barrón J, Attié F, Ovseyevitz J, Pinto Tortolero R, Rodas Estrada M A, Guadalajara J F, Huerta D, Esquivel Avila J
Arch Inst Cardiol Mex. 1982 Jul-Aug;52(4):319-22.
Echocardiographic recognition of pulmonary atresia with either ventricular septal defect or intact ventricular septum is of great value in the differential diagnosis with other forms of right ventricular outflow tract obstruction or hypoplasia of the right ventricle. We studied nine patients with pulmonary atresia seven with ventricular septal defect and two with intact ventricular septum. It was not possible in either group of these patients to register systolic opening and diastolic closure movements of the pulmonary valve. In the group with ventricular septal defect, aortic straddling was present in all cases. In one patient it was possible to register the echoes of an imperforated pulmonary valve. In the remaining patients, the differential diagnosis with persistent truncus arteriosus was not possible. M-mode and Two-dimensional echocardiographic features of pulmonary atresia with intact ventricular septum are specific of this malformation and can differentiate it from other forms of hypoplasia of the right ventricle.
超声心动图对伴有室间隔缺损或室间隔完整的肺动脉闭锁的识别,在与其他形式的右心室流出道梗阻或右心室发育不全的鉴别诊断中具有重要价值。我们研究了9例肺动脉闭锁患者,其中7例伴有室间隔缺损,2例室间隔完整。在这些患者的任何一组中,均无法记录到肺动脉瓣的收缩期开放和舒张期关闭运动。在伴有室间隔缺损的组中,所有病例均存在主动脉骑跨。在1例患者中,能够记录到未穿孔肺动脉瓣的回声。在其余患者中,无法与永存动脉干进行鉴别诊断。室间隔完整的肺动脉闭锁的M型和二维超声心动图特征是这种畸形所特有的,并且可以将其与右心室发育不全的其他形式区分开来。