Key result
Emergent adrenalectomy with Impella and VA-ECMO successfully treats pheochromocytoma-triggered Takotsubo shock, improving LVEF to 35%.
Why the study?
Pheochromocytoma-related Takotsubo syndrome is uncommon but tends to be severe, with ischaemia/vasospasm, pulmonary oedema, arrhythmias, and shock.
Case Report (n=1)
Pheochromocytoma-triggered Takotsubo syndrome can rapidly progress to cardiogenic shock requiring early mechanical circulatory support and definitive tumor resection.
May warrant mechanical support plus urgent resection in refractory pheochromocytoma-Takotsubo shock; leaves open generalizability and optimal protocols.
Background Takotsubo syndrome may follow an abruptadrenergic discharge; pheochromocytoma–related forms are uncommon but tend to be severe, with ischaemia/vasospasm, pulmonary oedema, arrhythmias and shock. Case presentation A 57–year–old woman with long–standing paroxysmal hypertension and a 5–cm right adrenal mass wasadmitted for morpho–functional assessment of suspectedpheochromocytoma. During the diagnostic pathway, shortly after corticosteroid exposure, she suddenly developed a fulminantadrenergic crisis (extreme hypertension, tachyarrhythmias), rapidly progressing to acute pulmonary oedema, severe lacticacidosis, hyperosmolar coma and cardiogenic shock. ECG showeddiffuse repolarization abnormalities with deep T-wave inversionand QTc prolongation. Transthoracic echocardiographydemonstrated mid–apical akinesia with basal hyperkinesis(Takotsubo pattern) and LVEF ∼25%; coronary angiographyexcluded obstructive disease. Despite vasoactive support, she required Impella left–ventricular assistance and escalation to veno–arterial ECMO. The course was complicated by sustainedventricular tachycardia and ventricular fibrillation, treated with lidocaine, esmolol and defibrillation, and later by an episode of atrial fibrillation. Emergent adrenalectomy under mechanicalsupport removed a pheochromocytoma, after which blood–pressure lability eased and ventricular function began to recover(LVEF 35% on step–down). She was discharged stable on guideline–directed heart–failure therapy and scheduled for cardiacMRI. Conclusions This case illustrates a clinically relevant “double hit”: diagnostic work–up (and potentially steroids) acting as the spark for catecholamine storm and Takotsubo syndrome, with malignant arrhythmias and multiorgan failure.In suspectedpheochromocytoma, clinicians should actively avoid precipitants, ensure early alpha–blockade, and use beta–blockers only after adequate alpha–control. Early transfer to centres able to providerapid mechanical circulatory support and definitive tumourresection can be lifesaving
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Barnaba et al. (2026) conducted a case report in Pheochromocytoma-triggered Takotsubo syndrome (n=1). Impella, VA-ECMO, and emergent adrenalectomy was evaluated. Emergent adrenalectomy under mechanical support (Impella and VA-ECMO) successfully treated a 57-year-old woman with pheochromocytoma-triggered Takotsubo shock, improving LVEF from ~25% to 35%.
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