PDF(Pubmed)
Abstract：
Brugada syndrome (BrS) is a congenital channelopathy associated with an increased risk of malignant ventricular arrhythmias and sudden cardiac death in individuals without any structural cardiopathy. Brugada phenocopies (BrPs) are clinical entities that present electrocardiographic patterns similar to those of BrS that are elicited only under transitory pathophysiological conditions, with normalization of the ECG pattern after the resolution of those conditions. We present a rare case of BrP due to intracranial hemorrhage. We also present and discuss the diagnostic criteria for BrPs and their application to this case.
摘要：
Brugada综合征（BrS）是一种先天性通道病，与无任何结构性心脏病的个体中恶性室性心律失常和心源性猝死的风险增加有关。Brugada表型（BrPs）是临床实体，表现出与BrS相似的心电图模式，仅在短暂的病理生理条件下引起。在解决这些情况后，对ECG模式进行归一化。我们介绍了由于颅内出血引起的罕见BrP病例。我们还介绍并讨论了BrPs的诊断标准及其在这种情况下的应用。
