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Vol. 17. Núm. 4.
Páginas 177-186 (Julio - Agosto 2010)
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Vol. 17. Núm. 4.
Páginas 177-186 (Julio - Agosto 2010)
Open Access
Síndrome de Brugada en un paciente con síncope. Presentación de un caso y revisión de la literatura
Brugada syndrome in a patient with syncope. A case report and literature review
Visitas
3807
Carlos J. Jaramillo1, Luis F. Perdomo1, Esteban Cardona1, Gabriel A. Londoño1,
Autor para correspondencia
thegabo10@gmail.com

Correspondencia: Calle 50 B sur No. 42 C - 21 Unidad la Hojarasca, Casa 414. Medellín, Colombia. Tel 378 18 58 - Cel.: 300 266 73 49.
1 Facultad de Medicina, Universidad de Antioquia. Medellín, Colombia
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Información del artículo

El síndrome de Brugada es una enfermedad autosómica dominante esporádica que afecta los canales de sodio de los miocardiocitos. Clínicamente se caracteriza por síncopes recurrentes y/o muerte súbita, que en el electrocardiograma simula un bloqueo de rama derecha, acompañado de elevación peculiar del segmento ST en las derivaciones precordiales derechas (V1, V2 y V3) sin alteración cardiaca estructural. Afecta principalmente a hombres en la cuarta década de la vida y tiene mayor prevalencia en el suroeste asiático. El caso que se describe corresponde a un paciente con antecedentes personales de síncopes, a quien se le encuentra un patrón electrocardiográfico tipo-2 de Brugada y quien además tiene un hermano con historia de síncopes. Con una prueba de mesa basculantes positivo para síncope mediado neuralmente se deja este diagnóstico, pero no se descarta la sospecha inicial de síndrome de Brugada.

Palabras clave:
síndrome de Brugada
síncope
muerte súbita
arritmias
patrones electrocardiográficos tipo Brugada
canales de sodio cardiacos
bloqueadores de canales de sodio

Brugada syndrome is a sporadic autosomal dominant genetic disease that affects cardiac sodium channels. It is clinically characterized by recurrent syncope and/or sudden death with electrocardiographic manifestations that simulate a right bundle branch block accompanied by ST-segment elevation in the right precordial leads (V1, V2 and V3) without structural cardiac changes. It mainly affects men in their fourth decade and is most prevalent in southwestern Asia. We present the case of a patient with history of syncope, type-2 Brugada electrocardiographic pattern and who has a brother also with history of syncope. The patient had a positive tilt test for neurocardiogenic syncope. He was diagnosed as neurocardiogenic syndrome, without discarding the initial suspicion of Brugada syndrome.

Key words:
Brugada syndrome
syncope
sudden death
arrhythmias
Brugada-type electrocardiographic patterns
cardiac sodium channels
sodium channel blockers
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