Management of Adrenal Masses
Adrenal masses require a systematic approach including hormonal evaluation and imaging studies, with surgical intervention indicated for masses >4 cm, those with concerning radiological features (HU >20, inhomogeneous), or any hormone-producing tumors. 1
Initial Evaluation
Imaging Assessment
- Dedicated adrenal imaging is essential for all adrenal masses 1, 2
- Non-contrast CT is the first-line imaging modality
- HU ≤10: Benign adenoma (0% risk of adrenocortical carcinoma)
- HU >20: Increased suspicion for malignancy
- For indeterminate lesions, proceed with:
- Contrast-enhanced CT washout study (>60% washout at 15 minutes suggests benign lesion)
- Chemical shift MRI (particularly useful when CT contrast is contraindicated)
- FDG-PET for radiologically indeterminate cases with suspicion of malignancy
- Non-contrast CT is the first-line imaging modality
Hormonal Evaluation
All patients with adrenal masses ≥1 cm should undergo complete hormonal evaluation 1, 2:
Mandatory tests for all patients:
- 1-mg overnight dexamethasone suppression test (cortisol ≤50 nmol/L or ≤1.8 µg/dL is normal)
- Plasma-free or 24-hour urinary fractionated metanephrines (pheochromocytoma screening)
Additional tests:
- Aldosterone-to-renin ratio (especially in hypertensive patients)
- Electrolyte panel (to screen for hypokalemia in primary aldosteronism)
Management Algorithm
Surgical Management
Surgery is indicated for 1, 2:
- Masses >4 cm in diameter
- Masses with irregular margins or heterogeneous appearance
- High attenuation (>10 HU) on non-contrast CT
- Poor contrast washout (<60% at 15 minutes)
- Any hormone-producing tumor
- Growth >5 mm/year on follow-up imaging
Surgical Approach
- Minimally invasive surgery (MIS) is preferred for benign adenomas
- Open adrenalectomy should be considered for:
- Larger tumors
- Features concerning for malignancy
Non-Surgical Management
For benign-appearing adrenal adenomas 1, 2:
- <4 cm with HU ≤10: No further follow-up imaging or functional testing required
- ≥4 cm: Repeat imaging in 6-12 months
- Growth <3 mm/year: No further imaging or functional testing required
- Growth >5 mm/year: Repeat functional work-up and consider adrenalectomy
Special Considerations
Mild Autonomous Cortisol Secretion (MACS)
- Defined as cortisol >50 nmol/L (>1.8 µg/dL) after dexamethasone suppression test without overt Cushing's syndrome 2
- Screen for potential cortisol-related comorbidities (hypertension, type 2 diabetes)
- Consider surgical treatment in patients with relevant comorbidities 2
Perioperative Management
- Perioperative steroid coverage is mandatory for patients with cortisol-producing adenomas 1
- Gradual tapering of glucocorticoid replacement therapy with follow-up cortisol testing
Common Pitfalls and Caveats
Always exclude pheochromocytoma before any adrenal biopsy 1
- 1.5-14% of incidentally discovered adrenal masses are pheochromocytomas
- Failure to identify can lead to life-threatening hypertensive crisis during procedures
Correlation of imaging with biochemical testing is crucial 1
- Radiologically benign-appearing masses can still be hormonally active
Adrenal biopsy is rarely required 3
- Modern imaging techniques can characterize most adrenal masses
- Biopsy should be considered only after excluding pheochromocytoma and when diagnosis remains uncertain after comprehensive imaging
Size is not the only criterion for surgery
- Even smaller masses with concerning radiological features or hormonal activity require surgical management
The evidence strongly supports a systematic approach to adrenal masses, with the most recent guidelines emphasizing the importance of both imaging characteristics and hormonal evaluation in determining management strategy 1, 2.