Why the study?
Clinically significant cardiac sarcoidosis is rare in the absence of lung involvement but is associated with life-threatening complications.
Highlights the importance of considering cardiac sarcoidosis in patients presenting with unexplained acute heart failure and refractory tachyarrhythmias, which can respond to corticosteroid therapy.
May support steroid trial for refractory VT in cardiac sarcoidosis; hypothesis-generating and requires prospective validation.
Sarcoidosis is a multisystem granulomatous disorder that can involve any organ, most commonly the lungs. However, a minority of the patients (8%) presents with extrapulmonary disease that spares the lungs. Although clinically significant cardiac sarcoidosis is a rare occurrence in the absence of lung involvement, it is associated with life-threatening complications. We present a case of de novo cardiac sarcoidosis. The patient presented with symptoms of heart failure and resistant ventricular tachycardia. Fortunately, he responded well to anti-failure medications. Ventricular tachycardia subsided only after starting steroids. Further follow-up was not possible as the patient returned to his home country. Our report highlights the importance of considering cardiac sarcoidosis as a differential diagnosis in patients who present with unexplained heart failure and arrhythmias. • A rare case of fulminant de novo cardiac sarcoidosis presenting with acute heart failure and resistant tachyarrhythmia. • Unusual cardiac wall involvement confirmed by 18F-FDG PET scan. • Clinically isolated cardiac sarcoidosis with no pulmonary involvement. • Marked clinical improvement following initiation of corticosteroid therapy. • Highlights the need to consider cardiac sarcoidosis in patients with unexplained acute heart failure and refractory tachyarrhythmias.
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Hassan et al. (2025) studied this question.
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