Lincoln C, Anderson R H, Shinebourne E A, English T A, Wilkinson J L
Br Heart J. 1975 May;37(5):453-63. doi: 10.1136/hrt.37.5.453.
Four patients are described with a recently recognized variant of double outlet right ventricle. Clinical examination favoured tetralogy of Fallot, but the chest X-ray suggested corrected transposition. Catheterization and angiocardiography showed that the aorta was to the left of the main pulmonary artery, and both arose from a normally positioned morphological right ventricle. Egress of blood from the left ventricle was through a subaortic ventricular septal defect. In all patients severe pulmonary stenosis was present and the right coronary artery ran an anomalous course anterior to the pulmonary valve ring. Two children had successful total correction, and one a palliative Blalock-Taussing shunt. Necropsy material from the fourth patient allowed confirmation of the ventricular morphology and the conducting tissued was examined. In corrective surgery, blood from the left ventricle was rerouted into the aorta by an intraventricular baffle. Pulmonary stenosis was relived by infundibulectomy and outflow tract patch.
本文描述了4例患有最近才被认识的双出口右心室变异型的患者。临床检查倾向于法洛四联症,但胸部X线片提示矫正型大动脉转位。心导管检查和心血管造影显示主动脉位于主肺动脉左侧,二者均起自正常位置的形态学右心室。左心室血液通过主动脉下室间隔缺损流出。所有患者均存在严重的肺动脉狭窄,右冠状动脉走行异常,位于肺动脉瓣环前方。2例儿童成功接受了根治性手术,1例接受了姑息性布-塔分流术。第四例患者的尸检材料证实了心室形态,并对传导组织进行了检查。在矫正手术中,左心室的血液通过心室内挡板改道流入主动脉。通过漏斗部切除术和流出道补片缓解了肺动脉狭窄。