Anders H J, Fuchshuber S
Medizinische Poliklinik, Universität Munich, Pettenkoferstr. 8a, D-80336 Munich, Germany.
Eur J Med Res. 2001 Jun 28;6(6):275-6.
Pentalogy of Fallot is a rare cyanotic congenital heart disease characterized by biventricular origin of the aorta above a large ventricular septal defect, obstruction of the pulmonary outflow, right ventricular hypertrophy (tetralogy of Fallot), and an atrial septal defect. Mortality due to syncope, arrhythmia or congestive heart failure is about 75% by the age of 10 years and 97% by the age of 40. We report a 69-year old female with uncorrected pentalogy of Fallot who suffered from recurrent syncope during classic cyanotic spells. Treatment with bisoprolol is recommended in symptomatic children and also improved symptoms in our patient. We conclude that single patients with pentalogy of Fallot reach the seventh decade and that cyanotic congenital heart disease is a rare cause of syncope in the elderly.
法洛五联症是一种罕见的青紫型先天性心脏病,其特征为在大型室间隔缺损上方主动脉起源于双心室、肺流出道梗阻、右心室肥厚(法洛四联症)以及房间隔缺损。因晕厥、心律失常或充血性心力衰竭导致的死亡率在10岁时约为75%,40岁时约为97%。我们报告了一名69岁未矫正法洛五联症的女性患者,她在典型的青紫发作期间反复出现晕厥。对于有症状的儿童推荐使用比索洛尔治疗,我们的患者症状也得到了改善。我们得出结论,法洛五联症的单一患者可活到七十多岁,青紫型先天性心脏病是老年人晕厥的罕见原因。