Case Report (n=1)
This case highlights a rare presentation of bidirectional ventricular tachycardia caused by a combined phenotype of nonhypertrophic hypertrophic cardiomyopathy and channelopathy, which proved uniquely responsive to phenytoin.
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May support phenytoin in rare bidirectional VT with combined nonhypertrophic HCM-QTU phenotype; leaves open validation in larger cohorts.
Bidirectional ventricular tachycardia (BDVT), a rare ventricular arrhythmia, is commonly caused by digitalis toxicity or channelopathies and is rarely caused by aconite toxicity, myocarditis, infarction, or sarcoidosis. This paper describes a patient with BDVT, recurrent syncope, myocardial disarray, and interstitial fibrosis on histology but normal results on echocardiography with variants in the TTN, KCNH2, and GATA4 genes. (Level of Difficulty: Advanced.)
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Chakraborty et al. (2019) conducted a case report in Bidirectional ventricular tachycardia (n=1). Phenytoin and implantable cardioverter-defibrillator was evaluated.
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