Epidemiology


Etiology


Pathophysiology


Clinical features

  • Classic Triad (episodic, paroxysmal):
    1. Pounding headache.
    2. Diaphoresis (profuse).
    3. Tachycardia/Palpitations.
  • Refractory/Resistant HTN: Paroxysmal (50%) or persistent.
    • Sustained HTN (50–60% of cases): The majority of patients with pheochromocytoma actually have persistent, daily high blood pressure. c
    • Paroxysmal HTN (40–50% of cases): Spikes in blood pressure occur intermittently, often superimposed on normal blood pressure or baseline sustained HTN.
    • Normotension (~10% of cases): Patients may have normal blood pressure, particularly those diagnosed early via familial screening (e.g., VHL, MEN2).
  • Other features: Anxiety, panic-like attacks, orthostatic hypotension (due to low plasma volume), hyperglycemia (impairs insulin secretion/increases glycogenolysis). c
  • Triggers: Surgery/anesthesia induction, exercise, defecation, trauma, foods high in tyramine (cheese, red wine). c

Diagnostics


Differential diagnostics

ConditionKey Differentiating FeaturesConfirmatory Test
Anxiety/PanicPsychological triggers; lacks severe paroxysmal HTN; may respond to psychiatric meds.Normal metanephrines.
HyperthyroidismPersistent symptoms (not spells); goiter, proptosis; fine tremor.Low TSH, High T4/T3.
Carcinoid SyndromeClassic triad: Flushing, Diarrhea, Wheezing; right-sided heart valve disease.High urinary 5-HIAA.
Illicit Drug UseHistory of use; positive urine toxicology screen.Positive tox screen; metanephrines normalize with abstinence.
Clonidine WithdrawalHistory of abrupt clonidine cessation; symptoms resolve with clonidine re-administration.Clonidine suppression test.
Essential HTNOften asymptomatic; lacks paroxysmal spells; responds to standard antihypertensives.Normal metanephrines.

Treatment