Why the study?
Differentiating between sarcoidosis and giant cell myocarditis based on clinical presentation is difficult.
The presence of bidirectional ventricular tachycardia may help distinguish cardiac sarcoidosis from giant cell myocarditis in patients with fulminant myocarditis.
May support bidirectional VT as a differentiator in fulminant myocarditis; leaves open validation in larger cohorts.
Differentiating between sarcoidosis and giant cell myocarditis (GCM) based on clinical presentation is difficult. We present the case of a 57-year-old woman who was initially diagnosed with GCM based on endomyocardial biopsy. The patient was refractory to standard management for GCM and went on to develop bidirectional ventricular tachycardia, a finding suggestive of sarcoidosis. Unfortunately, the patient eventually needed cardiac transplantation. The explanted heart demonstrated cardiac sarcoidosis. Bidirectional ventricular tachycardia has not been demonstrated in GCM, and its presence may help in distinguishing between GCM and cardiac sarcoidosis.
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Durocher et al. (2021) studied this question.
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