Brugada Syndrome – Report of Familial Occurrence Diagnosed in the Emergency Department

IF 0.8 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Journal Of Cardiovascular Emergencies Pub Date : 2020-03-01 DOI:10.2478/jce-2020-0001
M. Fazel, F. Hamidi, E. Afshari
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Abstract

Abstract Introduction: Brugada syndrome represents the clinical manifestation of a rare disease with genetic etiology. The syndrome is characterized by ventricular dysrhythmias associated with syncope or sudden cardiac death in the lack of any structural cardiac disease. The diagnosis of Brugada syndrome is established if a type 1 electrocardiographic (ECG) pattern of ST-segment and QRS morphology is present, in association with certain clinical manifestations and/or familial history. Case presentation: A 31-year-old male patient, without any medical history, presented in the emergency department (ED) of a clinical center. His only complaints consisted in palpitations, chest discomfort, and emotional stress related to the recent death of his wife. Earlier on the same day, his wife, a 25-year-old female was brought via emergency medical services (EMS) to the ED after presenting ventricular fibrillation. The female patient presented a long term history of chest pain and one year prior to this episode she presented idiopathic ventricular fibrillation, for which she had undergone implantation of an automated cardioverter defibrillator. As the couple were cousins, the EMS specialist suspected the presence of a familial cardiac disorder. The electrocardiogram of the male patient revealed a coved-type ST-segment elevation of 4 mm in leads V1–V3 compatible with type 1 Brugada syndrome. Conclusion: In case of Brugada syndrome, a genetic disorder associated with increased risk of SCD, the patient's first-degree relatives should be investigated as well, in order to identify the presence of the syndrome and to prevent SCD. As the sole established effective therapeutic measure for patients diagnosed with Brugada syndrome, ICD implantation should be considered in order to decrease the risk of syncope and SCD. This case is particular because a rare disease with familial etiology was identified in both husband and wife, who were cousins.
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Brugada综合征——在急诊科诊断的家族性发生报告
摘要简介:Brugada综合征是一种罕见的遗传病的临床表现。该综合征的特征是室性心律失常伴晕厥或心源性猝死,但无任何结构性心脏病。如果存在st段和QRS形态的1型心电图(ECG)模式,并与某些临床表现和/或家族史相关,则可以确定Brugada综合征的诊断。病例介绍:31岁男性患者,无任何病史,于临床中心急诊科就诊。他唯一的主诉是心悸、胸部不适和与他妻子最近去世有关的情绪紧张。同日早些时候,他的妻子,一名25岁的女性,在出现心室颤动后被紧急医疗服务(EMS)送到急诊科。该女性患者有长期胸痛病史,在此发作前一年,她出现特发性心室颤动,为此她植入了自动心律转复除颤器。由于这对夫妇是表亲,急救专家怀疑他们患有家族性心脏疾病。男性患者心电图显示V1-V3导联st段抬高4mm,符合1型Brugada综合征。结论:Brugada综合征是一种与SCD风险增加相关的遗传性疾病,对于Brugada综合征,患者的一级亲属也应进行调查,以确定该综合征的存在并预防SCD。作为Brugada综合征患者唯一确定有效的治疗措施,应考虑植入ICD,以降低晕厥和SCD的风险。这个病例是特别的,因为一种罕见的家族性病因的疾病被发现在夫妻双方,谁是表兄弟。
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审稿时长
8 weeks
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