DOI: https://doi.org/10.36347/sjmcr.2025.v13i08.014

Pages: 1811-1814

Introduction: Pheochromocytoma is a rare catecholamine-secreting tumour that can mimic acute myocarditis and lead to life-threatening cardiogenic shock. We present a case of recurrent fulminant myocarditis ultimately attributed to an adrenal pheochromocytoma. Case presentation: A 34-year-old woman with no cardiovascular risk factors experienced recurrent myocarditis over 18 months. During her third episode, she developed cardiogenic shock with multiorgan failure. An abdominal ultrasound revealed a left adrenal mass, confirmed by CT scan. Elevated urinary catecholamine metabolites established the diagnosis of pheochromocytoma. Following emergency adrenalectomy, her haemodynamic status stabilised, and she recovered fully. Discussion: Recurrent myocarditis or unexplained cardiogenic shock should prompt consideration of secondary causes, including pheochromocytoma. Early recognition and multidisciplinary management are key to favourable outcomes.