adrenal incidentalomas
- 4% of Pts undergoing abdominal CT scan have incidentally discovered adrenal mass;
- prevalence ↑ with age
Differential diagnosis
- Nonfunctioning mass:
- adenoma,
- cysts,
- abscesses,
- granuloma,
- hemorrhage,
- lipoma,
- myelolipoma,
- primary or metastatic malignancy
- Functioning mass:
- pheochromocytoma,
- adenoma (cortisol, aldosterone, sex hormones),
- other endocrine tumor,
- carcinoma
Hormonal workup (EJE 2016;175:G1; NEJM 2021;384:1542)
一般不做 bx
- Rule out subclinical Cushing’s Syndrome
- in all Pts using 1 mg overnight DST (Sp 91%).
- Abnormal results require confirmatory testing.
- Rule out hyperaldosteronism
- if hypertensive w/ plasma aldo & renin (see above)
- Rule out pheochromocytoma
- in ALL Pts (b/c of morbidity unRx’d pheo)
- using 24-h urine fractionated metanephrines or plasma fractionated metanephrines
- Malignancy workup-adrenal incidentalomas
Follow-up
- If hormonal workup ⊖ and appearance benign,
- no further follow-up imaging needed,
- but controversial (Annals 2019;171:107)
- biochemical testing to detect pheochromocytoma and excess cortisol secretion, and those who also have high blood pressure should undergo biochemical testing to detect primary hyperaldosteronism
- Patients with pheochromocytoma should undergo adrenalectomy after adequate presurgical alpha-blockade and beta-blockade, if necessary.
- Patients with mild autonomous cortisol excess and primary hyperaldosteronism may benefit from adrenalectomy, but treatment should be individualized.
- Nonfunctioning adrenal tumors that have an attenuation of 10 Hounsfield units or less on computed tomographic (CT) evaluation and that are smaller than 4 cm in greatest diameter generally do not warrant intervention or long-term follow-up.
- All other adrenal incidentalomas with indeterminate features on imaging may warrant additional imaging with contrast-enhanced CT,
- magnetic resonance imaging with chemical-shift analysis,
- positron-emission tomography–CT with 18F-fluorodeoxyglucose, or all of these tests.