Ozeke Ozcan, Cavus Umut Y, Atar Ilyas, Ozin Bulent, Ilkay Erdogan
Department of Cardiology, MESA Hospital, Ankara, Turkey.
Ann Noninvasive Electrocardiol. 2009 Jul;14(3):305-8. doi: 10.1111/j.1542-474X.2009.00302.x.
Both Brugada syndrome (BrS) and arrhythmogenic right ventricle dysplasia/cardiomyopathy (ARVD/C) can cause repolarization abnormalities in right precordial leads and predispose to sudden cardiac death (SCD) due to ventricular arrhythmias. Although there is controversy over whether BrS is distinct from ARVD/C, it is believed that both are different clinical entities with respect to both the clinical presentation and the genetic predisposition. The coexistence of these two relatively rare clinical entities is also reported, but, some hypothesized that it is more possible that disease of the right ventricular muscle might accentuate the Brugada electrocardiographic pattern. In clinic practice, there may be cases where the dividing line is not so clear. We report a 33-year-old male presenting with recurrent syncope, who has a peculiar pattern of coved-type ST-segment elevation (ST-SE) with epsilon-like wave in right precordial leads.
Brugada综合征(BrS)和致心律失常性右心室发育不良/心肌病(ARVD/C)均可导致右胸前导联复极异常,并因室性心律失常而易发心脏性猝死(SCD)。尽管对于BrS是否有别于ARVD/C存在争议,但人们认为二者在临床表现和遗传易感性方面均为不同的临床实体。也有这两种相对罕见临床实体共存的报道,不过,有人推测右心室肌疾病更有可能使Brugada心电图模式加重。在临床实践中,可能存在分界线不那么清晰的病例。我们报告一名33岁男性,反复出现晕厥,其右胸前导联有特殊的穹窿型ST段抬高(ST-SE)伴类ε波。