Treatment Algorithm for Adrenal Incidentaloma
The treatment algorithm for adrenal incidentaloma should follow a structured approach based on radiologic characteristics, hormonal evaluation, and size criteria to determine management decisions, with surgical intervention indicated for functional tumors, suspicious imaging features, or significant growth. 1
Initial Evaluation
Radiologic Assessment
- First-line imaging: Non-contrast CT to determine if the mass is benign or malignant 1
Hormonal Evaluation
- All patients should undergo screening for autonomous cortisol secretion with 1 mg overnight dexamethasone suppression test 2, 3
- Patients with hypertension and/or hypokalemia should be screened for primary aldosteronism with aldosterone-to-renin ratio 1, 2
- Patients with adrenal masses >10 HU on non-contrast CT or with symptoms of catecholamine excess should be screened for pheochromocytoma with plasma or 24-hour urinary metanephrines 1, 2
- In cases of suspected adrenocortical carcinoma or virilization, perform serum androgen testing 1, 2
Management Decision Tree
Surgical Intervention Indicated For:
Functional tumors:
- Unilateral cortisol-secreting masses with clinically apparent Cushing's syndrome 1
- Aldosterone-secreting adrenal masses 1
- Pheochromocytomas 1
- Younger patients with mild autonomous cortisol secretion who have progressive metabolic comorbidities attributable to cortisol excess (after shared decision making) 1
Suspicious imaging features:
Growth during follow-up:
- Adrenal incidentalomas growing >5 mm/year (after repeating functional work-up) 1
Follow-up Without Surgery For:
Benign non-functional lesions <4 cm, myelolipomas, and other small masses containing macroscopic fat:
- No further follow-up imaging or functional testing required 1
Radiologically benign (<10 HU) but ≥4 cm non-functional lesions:
- Repeat imaging in 6-12 months 1
Lesions with minimal growth:
Indeterminate non-functional lesions:
- Management options include repeat imaging in 3-6 months versus surgical resection (shared decision-making) 1
Special Considerations
Bilateral Adrenal Incidentalomas
- Each lesion should be separately characterized following the same protocol as unilateral masses 1
- Consider measuring serum 17-hydroxyprogesterone to exclude congenital adrenal hyperplasia 1, 2
- Assess for adrenal insufficiency in suspected cases of bilateral infiltrative disease, metastases, or hemorrhage 1
Adrenal Biopsy
- Adrenal mass biopsy should not be performed routinely for the work-up of an adrenal incidentaloma 1
- Only consider when diagnosis of metastatic disease from an extra-adrenal malignancy would be of value 1
Common Pitfalls to Avoid
- Skipping hormonal evaluation even in apparently non-functioning tumors 3
- Relying solely on radiological appearance to predict hormone secretion status 3
- Performing adrenal biopsy without excluding pheochromocytoma, which can trigger life-threatening hypertensive crisis 3
- Failing to consider a multidisciplinary approach when imaging is not consistent with a benign lesion, there is evidence of hormone hypersecretion, significant tumor growth, or when surgery is being considered 1