Who should be screened for adrenal incidentaloma?

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Last updated: January 6, 2026View editorial policy

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Who Should Be Screened for Adrenal Incidentaloma?

All patients with an incidentally discovered adrenal mass on imaging performed for reasons unrelated to suspected adrenal disease require screening—this is the definition of an adrenal incidentaloma and mandates evaluation. 1, 2

Universal Screening Requirements

Every patient with an adrenal incidentaloma must undergo:

  • Autonomous cortisol secretion screening using a 1 mg overnight dexamethasone suppression test (1 mg at 11 PM, measure serum cortisol at 8 AM), regardless of clinical symptoms or imaging characteristics 1, 3, 4

  • Pheochromocytoma screening with plasma free metanephrines or 24-hour urinary fractionated metanephrines if the mass shows >10 HU on non-contrast CT OR if any signs/symptoms of catecholamine excess are present 1, 3, 5

  • Primary aldosteronism screening with aldosterone-to-renin ratio in all patients who have hypertension and/or hypokalemia 1, 3, 5

Exception to Pheochromocytoma Screening

The only scenario where you can skip pheochromocytoma screening is when the mass demonstrates unequivocal benign features on unenhanced CT (HU <10) AND the patient has no signs or symptoms of adrenergic excess 1. This is a narrow exception—when in doubt, screen.

Additional Screening in Specific Scenarios

  • Androgen excess testing (DHEA-S, testosterone, 17-hydroxyprogesterone, androstenedione) is required when clinical virilization signs are present OR when adrenocortical carcinoma is suspected 1, 3, 4

  • Bilateral adrenal masses require measurement of serum 17-hydroxyprogesterone to exclude congenital adrenal hyperplasia, in addition to evaluating each mass individually 1, 3, 5

Critical Context

The prevalence data justifies universal screening: approximately 5.3% of adrenal incidentalomas are cortisol-secreting adenomas, 5.1% are pheochromocytomas, and 1% are aldosterone-secreting adenomas 3, 4. Up to 30-50% may have mild autonomous cortisol secretion, which carries increased cardiovascular morbidity and metabolic risk 6.

Common Pitfalls to Avoid

  • Never skip hormonal evaluation even for radiologically benign-appearing masses, as imaging characteristics cannot reliably predict functional status 4, 7

  • Never perform adrenal biopsy before excluding pheochromocytoma—this can precipitate life-threatening hypertensive crisis 5, 4

  • Do not assume small size equals non-functional—hormone hypersecretion occurs independent of mass size and requires biochemical screening 1, 8

  • Medications can interfere with hormone testing results; hold interfering medications when possible before testing 3, 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Laboratory Tests for Adrenal Incidentaloma Follow-up

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Diagnostic Testing for Adrenal Adenoma

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Adrenal Nodules

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Approach to the Patient With Adrenal Incidentaloma.

The Journal of clinical endocrinology and metabolism, 2021

Research

Diagnosis and management of adrenal incidentalomas.

The Journal of urology, 2000

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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