Pérez Díaz L, Abasolo Olivares N, Nieves Gil A, Salado Marín M C, Moreno Granado F, Alonso Pulpón L
Servicio de Pediatría, Hospital Txagorritxu de Vitoria.
Rev Esp Cardiol. 1994 Jan;47(1):53-5.
Three cases of dilated cardiomyopathy manifested at 2, 5, and 13 months of age are reported. The clinical, radiographic, electrocardiographic, echocardiographic and angiocardiographic findings are analyzed. The follow up during 11, 14 and 16 years is described. After several years of the onset, 2 patients recovered a normal cardiac function. The third patient required a cardiac transplant when he was 9 years old, and now, after 2 and a half years, he is healthy, without congestive heart failure. Current references about indications of cardiac transplant in this disease are reviewed. We got the following conclusion: In patients with dilated cardiomyopathy, at least in those who begin before 2 years, the indication and the time of the cardiac transplant have to be established by individual valuation of each case, considering the follow up of the risk's criteria, mainly the congestive heart failure.
本文报告了3例分别在2个月、5个月和13个月时出现扩张型心肌病的病例。对其临床、影像学、心电图、超声心动图和心血管造影检查结果进行了分析。描述了11年、14年和16年的随访情况。发病数年后,2例患者心脏功能恢复正常。第3例患者9岁时接受了心脏移植,目前,在术后2年半,他身体健康,无充血性心力衰竭。本文回顾了目前关于该病心脏移植指征的参考文献。我们得出以下结论:在扩张型心肌病患者中,至少在2岁前发病的患者中,心脏移植的指征和时机必须根据每个病例的个体评估来确定,同时考虑风险标准的随访情况,主要是充血性心力衰竭。