What ECG findings are associated with pheochromocytoma?

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Last updated: March 15, 2026 • View editorial policy

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ECG Findings in Pheochromocytoma

The most characteristic ECG finding in pheochromocytoma is QT interval prolongation, which can be accompanied by ventricular arrhythmias, ST-T segment changes mimicking acute myocardial infarction, and prominent U waves. 1

Primary ECG Abnormalities

QT Prolongation and Ventricular Arrhythmias

  • Long QT interval is the hallmark ECG finding in patients with ventricular tachycardia associated with pheochromocytoma 1
  • Ventricular tachycardia and sudden cardiac death can occur, though the incidence is likely low and may be exacerbated by reversible catecholamine-induced hypertrophic or dilated cardiomyopathy 1
  • The dispersion of ventricular repolarization from QT prolongation creates the substrate for life-threatening arrhythmias including torsades de pointes, ventricular tachycardia, and ventricular fibrillation 2

U Wave Abnormalities

  • Prominent U waves appear in approximately 83% of untreated pheochromocytoma patients 2
  • The presence and magnitude of U waves correlate directly with urinary metanephrine levels (r²=0.333, p=0.015) and tumor size (r²=0.429, p=0.003) 2
  • After surgical removal, U wave prevalence drops dramatically from 91% to 9% 2
  • The number of leads showing U waves correlates with 3-methoxytyramine levels (r²=0.458, p=0.006) 2

ST-T Segment Changes

  • ST-segment depression or elevation and T-wave inversions frequently mimic acute myocardial infarction 3, 4, 5, 6
  • These ischemic-appearing changes occur despite normal coronary arteries on angiography 4, 5, 6
  • Right-sided pheochromocytomas may produce more striking electrocardiographic abnormalities 6
  • Alpha-adrenergic receptor blockade (phentolamine 10 mg) can normalize T-wave inversions, suggesting alpha-receptor involvement in these ECG changes 4

Additional ECG Manifestations

Rhythm Disturbances

  • Tachycardia and frequent ventricular ectopic beats are common 4, 6
  • Atrial flutter can occur 4
  • Supraventricular and ventricular arrhythmias requiring beta-blockade (after adequate alpha-blockade) 7

QRS Complex Changes

  • QRS prolongation may accompany electrolyte disturbances from catecholamine excess 1

Mechanism and Reversibility

The ECG abnormalities result from catecholamine-induced hyperactivation of the sympathetic nervous system with cardiac sympathetic nerve terminal disruption and norepinephrine spillover 3. These changes are characteristically reversible with appropriate alpha-adrenergic blockade and surgical tumor resection 1, 3, 2.

Clinical Pitfalls

  • Do not dismiss chest pain with ischemic ECG changes as acute coronary syndrome without considering pheochromocytoma, especially when troponin elevations are mild-to-moderate and coronary angiography shows normal arteries 5, 6
  • Fluctuating blood pressure combined with chest pain and ischemic ECG changes should raise suspicion for pheochromocytoma even without typical enzyme changes 6
  • Beta-blockade administered without prior alpha-blockade can paradoxically worsen ECG changes by unopposed alpha-receptor stimulation 4

Management Implications

  • Preoperative alpha-adrenergic blockade (phenoxybenzamine or doxazosin) helps prevent recurrence of ventricular arrhythmias 1
  • Beta-blockade should only be added after adequate alpha-blockade for persistent tachycardia, extrasystoles, or arrhythmias 7
  • Early definitive surgical treatment is a priority in cases with documented life-threatening arrhythmias 1
  • Intraoperative ventricular arrhythmias are treated with lidocaine 7

References

Research

Pheochromocytoma mimicking an acute myocardial infarction.

Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation, 2007

Research

Cardiovascular manifestations of pheochromocytoma.

The American journal of emergency medicine, 2000

Guideline

the american association of clinical endocrinologists and american association of endocrine surgeons medical guidelines for the management of adrenal incidentalomas.

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologist, 2009

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.