What are the symptoms of pheochromocytoma?

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Symptoms of Pheochromocytoma

The classic triad of symptoms in pheochromocytoma consists of headaches, palpitations, and sweating, typically occurring in an episodic fashion, with a diagnostic specificity of 90%. 1

Primary Clinical Manifestations

Pheochromocytomas are rare catecholamine-producing tumors that present with a constellation of symptoms related to catecholamine excess:

  • Cardiovascular symptoms:

    • Paroxysmal or sustained hypertension (50% have sustained hypertension) 1
    • Increased blood pressure variability 1
    • Palpitations
    • Orthostatic hypotension (especially in epinephrine-predominant tumors) 1
    • Arrhythmias
  • Neurological symptoms:

    • Headaches (often severe)
    • Anxiety or panic attacks
    • Tremors
  • Autonomic symptoms:

    • Episodic sweating (diaphoresis)
    • Pallor
    • Piloerection ("cold sweat") 1

Additional Presentations

  • Paroxysmal symptoms: Episodes or "spells" of symptoms that come and go, often lasting minutes to hours 1
  • BP lability: Dramatic fluctuations in blood pressure, which can be a distinguishing feature 1
  • Metabolic symptoms:
    • Weight loss
    • Hyperglycemia
    • Heat intolerance

Severe Manifestations

In severe cases, pheochromocytoma can present with:

  • Cardiogenic shock 2
  • Pulmonary edema 3
  • Cardiomyopathy 4
  • Electrical storm (multiple episodes of ventricular arrhythmias) 4
  • Total circulatory collapse requiring life support 3

Clinical Patterns

The presentation of pheochromocytoma is highly variable and can mimic many other diseases 5. Key patterns include:

  • Resistant hypertension: Hypertension that does not respond to standard treatment 1
  • Crisis presentation: Sudden, severe hypertension with end-organ damage 3
  • Incidental finding: Discovered during imaging for other reasons (adrenal incidentaloma) 1

Diagnostic Considerations

It's important to note that:

  • The average delay between initial symptoms and diagnosis is approximately 3 years 1
  • 55% of pheochromocytomas contribute to deaths and are not suspected in 75% of cases based on autopsy studies 1
  • Approximately 30% of pheochromocytomas are hereditary 1

Clinical Pitfalls

  • Symptoms can be intermittent, making diagnosis challenging
  • Many cases are missed entirely and only discovered at autopsy 1
  • The classic triad may not be present in all patients
  • Symptoms can be triggered by certain medications, physical activity, or procedures
  • Pheochromocytoma should be considered in any patient with unexplained paroxysmal symptoms, especially when associated with hypertension

Early recognition of these symptoms is crucial as pheochromocytoma can be life-threatening if undiagnosed or improperly managed, but it is typically curable with appropriate treatment 6.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Hypertensive crisis secondary to pheochromocytoma.

Proceedings (Baylor University. Medical Center), 2017

Research

Electrical Storm in a Case of Bilateral Pheochromocytomas.

The American journal of case reports, 2021

Research

Pheochromocytoma: evaluation, diagnosis, and treatment.

World journal of urology, 1999

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.

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