Lopez J A, Treistman B, Massumi A
Department of Cardiology, Texas Heart Institute, Houston 77030, USA.
Tex Heart Inst J. 1995;22(4):335-8.
We report the case of a 60-year-old man with long-standing symptomatic Wolff-Parkinson-White syndrome who presented with recurrent syncope and documented spontaneous ventricular fibrillation. This primary ventricular fibrillation, which was not preceded by atrial fibrillation, was associated with lymphocytic myocarditis and not with Wolff-Parkinson-White syndrome. The patient was treated with radiofrequency ablation of the accessory pathway and a drug regimen of prednisone, amiodarone, and metoprolol. At the 6-month follow-up, he was asymptomatic and had returned to work. To our knowledge, the association of acute lymphocytic myocarditis and Wolff-Parkinson-White syndrome has not been previously reported.
我们报告了一例60岁男性患者,患有长期有症状的预激综合征,出现反复晕厥且记录到自发性室颤。这种原发性室颤并非由房颤引发,而是与淋巴细胞性心肌炎相关,而非预激综合征。患者接受了旁路射频消融治疗以及泼尼松、胺碘酮和美托洛尔的药物治疗方案。在6个月的随访中,他无症状且已恢复工作。据我们所知,急性淋巴细胞性心肌炎与预激综合征的关联此前尚未见报道。