Variant Brugada syndrome--mild ST segment elevation in inferior leads and aborted sudden cardiac death
Kukla, P.; Jastrzebski, M.; Bacior, B.ła.; Gomuła, P.; Grodecki, J.; Kawecka-Jaszcz, K.
Kardiologia Polska 65(12): 1494-1498
2007
ISSN/ISBN: 0022-9032 PMID: 18181058 Document Number: 608089
We describe a case of an otherwise healthy 48-year-old man who survived aborted sudden cardiac death (SCD). His ECG showed ST segment elevation in inferior leads, therefore an acute coronary syndrome was suspected. However, serial troponin T and CPK-MB were negative, echocardiogram was unremarkable and exercise test was negative. On the basis of electrophysiological study, positive ajmaline test, persistent ST segment elevation in inferior leads and other clinical features (PQ interval of 240 ms, family history of SCD) a diagnosis of variant Brugada syndrome was made. Persistent ST segment elevations in inferior leads can be a marker of variant Brugada syndrome.