Management of Adrenal Nodules
All adrenal nodules require both imaging characterization and hormonal evaluation regardless of size, with surgical intervention indicated for nodules >4 cm, those with suspicious imaging features, or those demonstrating hormonal hypersecretion. 1
Initial Evaluation
Imaging Assessment
- Non-contrast CT is the first-line imaging modality 1
- HU < 10: Benign adenoma (0% risk of adrenocortical carcinoma)
- HU 10-20: Low risk of malignancy
- HU > 20: Higher risk of malignancy
- Size > 4 cm: Higher risk of malignancy 2
- Additional imaging options for indeterminate lesions:
- Contrast-enhanced CT: >60% washout at 15 minutes suggests benign lesion
- Chemical-shift MRI: Signal intensity loss in opposed-phase images indicates benign adenoma 1
Hormonal Evaluation
All adrenal nodules require complete hormonal evaluation regardless of size 1:
- 1mg overnight dexamethasone suppression test (cortisol ≤50 nmol/L or ≤1.8 μg/dL indicates normal suppression) 3
- Plasma or 24-hour urinary metanephrines (for pheochromocytoma)
- Aldosterone-to-renin ratio (for primary aldosteronism, especially in hypertensive patients)
- Consider sex hormones (DHEA-S, 17-OH-progesterone, androstenedione, testosterone) if adrenocortical carcinoma suspected 1
Management Algorithm
1. Benign Non-functional Adenomas
- For nodules <4 cm with benign imaging features (HU <10):
- For nodules ≥4 cm with benign imaging features:
2. Indeterminate Non-functional Lesions
- Options include:
- All patients with indeterminate imaging should be discussed in a multidisciplinary team 2, 3
3. Functional Lesions
- Pheochromocytoma: Surgical resection after appropriate alpha-blockade 1
- Cortisol-secreting adenoma (including mild autonomous cortisol secretion):
- Aldosterone-producing adenoma: Adrenalectomy for unilateral aldosterone production 1
4. Suspicious for Malignancy
- Surgical resection indicated for:
- Surgical approach:
Special Considerations
Bilateral Adrenal Nodules
- Each lesion should be separately characterized using the same criteria as unilateral nodules
- Consider congenital adrenal hyperplasia (measure serum 17-hydroxyprogesterone)
- Assess for adrenal insufficiency in suspected cases of bilateral infiltrative disease, metastases, or hemorrhage 2, 1
Young Adults, Children, and Pregnant Patients
- Require expedited evaluation due to higher risk of malignancy
- Consider MRI instead of CT to reduce radiation exposure 1
Follow-up Recommendations
For Non-operated Patients
- Benign, non-functional nodules <4 cm: No follow-up required 2, 1
- Benign, non-functional nodules ≥4 cm: Repeat imaging in 6-12 months 2
- Indeterminate nodules: Repeat imaging in 3-6 months 2, 1
- Mild autonomous cortisol secretion: Annual screening for cortisol-related comorbidities 3
Post-surgical Follow-up
- Clinical, imaging, and biochemical screening for at least 10 years for patients with adrenocortical carcinoma 1
Potential Pitfalls
- Failure to exclude pheochromocytoma before invasive procedures
- Delaying evaluation of suspicious nodules in young patients
- Performing unnecessary biopsies (adrenal mass biopsy is rarely indicated)
- Missing mild autonomous cortisol secretion 1
The management of adrenal nodules requires a systematic approach focusing on imaging characteristics, hormonal evaluation, and size to determine the appropriate treatment strategy and follow-up plan.