Hormone Workup for a 1.5 cm Left Adrenal Adenoma
All patients with adrenal incidentalomas, regardless of size, should be screened for autonomous cortisol secretion using a 1 mg overnight dexamethasone suppression test. 1
Universal Screening Required
- 1 mg dexamethasone suppression test (DST) is mandatory for all adrenal incidentalomas, taken at 11 PM with serum cortisol measured at 8 AM the following morning 1, 2
Conditional Screening Based on Clinical Features
Screen for Primary Aldosteronism IF:
- Patient has hypertension and/or hypokalemia 1, 2
- Measure aldosterone/renin ratio (ARR) in the morning after patient has been upright for 2 hours and seated for 5-15 minutes 1
- ARR >20 ng/dL per ng/mL/hr has >90% sensitivity and specificity for hyperaldosteronism 1
- Ensure patient is potassium-replete and substitute interfering medications when possible 1, 2
Screen for Pheochromocytoma IF:
- Mass measures ≥10 HU on non-contrast CT OR HU value is unavailable 1, 2
- Patient has symptoms of catecholamine excess (headaches, palpitations, sweating, anxiety attacks) 1
- Measure plasma free metanephrines or 24-hour urinary metanephrines 1, 2
- Values >2X upper limit of normal are significant 1
Important caveat: You can skip pheochromocytoma screening if the mass is unequivocally <10 HU on non-contrast CT AND the patient has no adrenergic symptoms 1
Screen for Androgen Excess IF:
- Clinical signs of virilization are present (hirsutism, acne, voice deepening, clitoromegaly, menstrual irregularities) 1, 2
- Adrenocortical carcinoma (ACC) is suspected based on imaging features (inhomogeneous, irregular margins, >4 cm) 1
- Measure DHEA-S and testosterone as initial tests 1, 2
- Extended panel if positive: 17β-estradiol, 17-OH progesterone, androstenedione, 17-OH pregnenolone, 11-deoxycorticosterone, progesterone, and estradiol 1
Critical Imaging Context
Before finalizing the hormone workup, confirm the mass characteristics on non-contrast CT 1, 2:
- If <10 HU (lipid-rich adenoma), pheochromocytoma screening can be omitted unless symptoms are present 1
- If ≥10 HU or indeterminate, proceed with full pheochromocytoma screening 1
Common Pitfalls to Avoid
- Never skip cortisol screening even for small masses—autonomous cortisol secretion occurs in 5-30% of incidentalomas and impacts morbidity through metabolic complications 1, 2
- Never perform adrenal biopsy before ruling out pheochromocytoma, as this can precipitate hypertensive crisis 1
- Do not assume a small mass is non-functional—even 1.5 cm masses can be hormonally active, particularly for aldosterone-secreting adenomas 3
- Recognize that co-secretion of multiple hormones (cortisol + androgens, cortisol + catecholamines) can occur and raises concern for ACC 4, 5, 6
Ancillary Testing if Abnormalities Found
- If cortisol hypersecretion confirmed: measure plasma ACTH to confirm ACTH-independent secretion 1
- If primary aldosteronism confirmed: perform adrenal vein sampling before considering surgery to lateralize the source 1
- If pheochromocytoma suspected: consider genetic testing for hereditary syndromes (VHL, MEN2, familial paraganglioma) 1