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Symptom approachAdrenal

Adrenal Incidentaloma

An adrenal incidentaloma is an adrenal mass found by chance on imaging — and every one must be triaged with exactly two questions: is it functioning (hormones) and is it malignant (imaging phenotype + size).

Q1
functioning?
+
Q2
malignant?
+
Never
biopsy before metanephrines
Orientation

The big picture

Cross-sectional imaging frequently finds adrenal masses. Most are benign non-functioning adenomas, but a minority are hormonally active (cortisol, aldosterone, catecholamines) or malignant (adrenocortical carcinoma or metastasis). The job is to sort each mass along those two axes.

Golden rule

Every incidentaloma gets two questions — functioning? (hormones) and malignant? (imaging + size) — and you exclude phaeochromocytoma before any biopsy.

Safety

Red flags

Mass + paroxysmal hypertension/spells

Phaeochromocytoma — metanephrines; alpha-blockade before any surgery; never biopsy first.

Large (>4 cm), lipid-poor, heterogeneous mass

Suspicious for adrenocortical carcinoma — surgical referral, avoid biopsy.

Indeterminate mass with known cancer

Consider metastasis — but exclude phaeochromocytoma before biopsy.

Presentation

Symptom sorter

Screen the hormones in every case.

Overnight dexamethasone suppression test (autonomous cortisol)Plasma or 24h urinary metanephrines (phaeochromocytoma)Aldosterone:renin ratio if hypertensive/hypokalaemicAndrogens if virilising features
Work-up

Diagnostic algorithm

Each step answers one question. Tap to expand.

Management

Treatment ladder

Treat based on the two questions: remove functioning tumours and those suspicious for malignancy; surveil benign non-functioning small masses.

1
Two-question work-up
2
Functioning → treat the hormone / operate
3
Phaeo → alpha-blockade then adrenalectomy
4
Suspicious/large → adrenalectomy
5
Benign non-functioning small → surveillance
Safety

Complications

Disease complications
  • Missed phaeochromocytoma (crisis)
  • Missed cortisol/aldosterone excess (cardiometabolic harm)
  • Missed adrenocortical carcinoma
Treatment complications
  • Unnecessary adrenalectomy for benign adenomas
  • Biopsy-precipitated phaeochromocytoma crisis
How to prevent
  • Apply the two questions to every mass
  • Never biopsy before excluding phaeochromocytoma
How to manage
  • Refer functioning/suspicious masses for surgery; surveil benign ones
Reference

Summary tables

The two-question framework

QuestionTestsIf positive
Functioning?DST, metanephrines, ARR, androgensTreat/operate for the hormone
Malignant?HU, washout, size, growthAdrenalectomy (en bloc if ACC)
Both negative, smallSurveillance
Recall

Memory hooks

Two questions: functioning? malignant?

Screen everyone: DST + metanephrines (± ARR).

Benign adenoma = low HU + good washout.

Big, lipid-poor, growing = think cancer.

Never biopsy before metanephrines.

Exam

Board traps

Adrenal mass biopsied → hypertensive crisis (it was a phaeo).

Non-functioning 5 cm lipid-poor mass observed instead of resected.

Resistant hypertension + hypokalaemia ignored (missed aldosteronoma).

Apply

Clinical cases

Case 1

A 55-year-old has a 2.5 cm adrenal mass found on a CT for back pain. It measures 6 HU unenhanced with good washout. BP is normal.

What work-up is required and what is the likely outcome?

Test yourself

Quiz

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