Makaryus Amgad N, Aronov Iosif, Diamond Joseph, Park Chong H, Rosen Stacey E, Stephen Bibiana
Division of Cardiology, North Shore-Long Island Jewish Health System, Long Island Jewish Medical Center, New Hyde Park, New York 11040, USA.
Echocardiography. 2004 Oct;21(7):631-7. doi: 10.1111/j.0742-2822.2004.03160.x.
Tetralogy of Fallot is the most common cyanotic congenital heart defect during infancy. It is composed of a ventricular septal defect, an overriding aorta, obstruction of right ventricular outflow, and right ventricular hypertrophy. Most patients experience cyanosis at birth and die in childhood without surgical intervention. The rate of survival at 40 years without surgical correction is only 3%. We present the case of a man with tetralogy of Fallot who survived until the age of 52 years without surgical intervention.
法洛四联症是婴儿期最常见的青紫型先天性心脏缺陷。它由室间隔缺损、主动脉骑跨、右心室流出道梗阻和右心室肥厚组成。大多数患者出生时即出现青紫,若不进行手术干预,会在儿童期死亡。未经手术矫正活到40岁的几率仅为3%。我们报告一例法洛四联症男性患者,未经手术干预活到了52岁。