Rare tumor of adrenal medulla secreting excessive catecholamines (epinephrine, norepinephrine). Causes episodic or sustained hypertension, severe headaches, palpitations, excessive sweating, tremor, and anxiety. Classic triad: headache, sweating, and tachycardia. Can cause hypertensive crisis if untreated. Most benign but ~10% malignant. Life-threatening if undiagnosed.
Malignant pheochromocytoma, or during active treatment phase (6 months post-treatment then re-evaluate)
Severe residual effects or benign tumor not amenable to surgery with ongoing symptoms
Moderate residual cardiovascular symptoms requiring multiple medications
Mild residual hypertension or anxiety controlled with medication
Post-surgical removal, asymptomatic, benign tumor with no recurrence
Medical Evidence
Current diagnosis from a qualified healthcare provider, medical records documenting symptoms and treatment history
Service Connection
Evidence linking your condition to military service (service treatment records, incident reports, or nexus letter)
Personal Statement
Your detailed account of how pheochromocytoma affects your daily life and when symptoms began
Lay Evidence
Buddy letters from fellow service members or family who can corroborate your symptoms
During your Compensation & Pension exam for pheochromocytoma, examiners will assess your symptoms against the rating criteria above.
Be specific: Describe your worst day, not your average day
Document everything: Bring copies of all medical records and evidence
Functional impact: Explain how symptoms affect work, sleep, and daily activities
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