Key result
Sequential blockade followed by adrenalectomy resolves pheochromocytoma-induced cardiomyopathy and normalizes metanephrines.
Case Report (n=1)
No
Pheochromocytoma-induced catecholamine crisis can present as cardiogenic shock mimicking diabetic ketoacidosis or sepsis, but cardiac function is highly reversible following appropriate medical blockade and surgical resection.
A pheochromocytoma is a rare catecholamine-secreting tumor that can cause life-threatening complications. Circulatory shock with a significant cardiogenic component is an uncommon initial presentation. This case describes a previously healthy 30-year-old woman presenting with vomiting, hyperglycemia, and shock. This rapidly progressed to requiring intubation, vasopressor therapy, and resuscitation following cardiac arrest. Imaging revealed a right adrenal mass and plasma metanephrines and normetanephrines were markedly elevated. After stabilization with α- and β-adrenergic blockade, the patient underwent successful adrenalectomy, confirming a pheochromocytoma-induced catecholamine crisis, with full recovery of cardiac function. This case illustrates the diversity of initial presentation of pheochromocytoma, the diagnostic challenges associated with measuring plasma (nor)metanephrines after resuscitation and the reversible nature of catecholamine-induced cardiomyopathy.
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Linden et al. (2026) conducted a case report in Pheochromocytoma-induced cardiogenic shock (n=1). Adrenalectomy and alpha/beta-adrenergic blockade was evaluated on Recovery of cardiac function.
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