Adrenal adenoma
Last updated: 10 July 2026
Reviewed by: Specialist doctors from the Elfcare quality team
Unexplained weight gain around the middle, blood pressure that won't come down despite medication, ongoing fatigue, or low potassium that keeps recurring for no clear reason: these can all point to a tumor called adrenal adenoma. Just as often, though, there are no symptoms at all, and the adenoma turns up as a small mass on an abdominal scan done for something else entirely. Either way, the same workup applies: finding out whether the tumor is affecting your hormones.
Adrenal adenomas are the most common adrenal incidentaloma, found in approximately 3 to 7% of abdominal MRI scans in adults. Most are entirely benign and produce no hormones. But a clinically meaningful share do produce excess hormones, and left unchecked, that can quietly damage the heart, bones, and metabolism over years. That's why a comprehensive hormonal blood panel alongside the MRI finding is the essential next step after discovery.
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What is an adrenal adenoma?
The adrenal glands are tiny, triangle-shaped organs sitting on top of each kidney that produce essential hormones controlling your blood pressure, metabolism, and stress response. An adrenal adenoma is a benign (non-cancerous) tumor that grows in the outer layer of this gland.
Adrenal adenomas are classified by whether they are active and pumping out extra hormones:
Non-functioning adenomas: the most common type (70% to 80% of cases). They do not produce any hormones, cause no symptoms, and are typically just monitored over time to ensure they stay stable.
Cortisol-secreting adenomas: these overproduce the stress hormone cortisol. This can lead to Cushing’s syndrome, causing hidden health issues like high blood pressure, diabetes, and weakened bones (osteoporosis).
Aldosterone-secreting adenomas (Conn’s adenoma): these flood the body with aldosterone, a hormone that regulates salt and water balance. This triggers severe high blood pressure and dangerously low potassium levels.
Androgen-secreting adenomas: a very rare type that produces excess male sex hormones, causing physical masculinising changes in women. Unlike other functioning adenomas, tumours that secrete androgens are disproportionately likely to be malignant rather than benign, so these findings are investigated with particular care.
The distinction between a functioning and non-functioning adenoma is the most important clinical question after an adrenal adenoma is identified and is answered through hormonal blood testing.
Symptoms of adrenal adenomas
Non-functioning adenomas cause no symptoms. Functioning adenomas cause symptoms reflecting the specific hormone produced in excess.
Cortisol-secreting adenoma:
Central weight gain with thin limbs
Round, flushed face
Purple stretch marks on the abdomen, thighs, and upper arms
Easy bruising and thin skin
Hypertension and diabetes
Muscle weakness, particularly proximal limb weakness
Osteoporosis and increased fracture risk
Low mood, depression, and cognitive difficulties
Subclinical cortisol secretion causes metabolic and cardiovascular consequences without the classic physical features above
Aldosterone-secreting adenoma:
Hypertension, often severe and resistant to standard treatment
Low potassium causing muscle weakness, cramps, and fatigue
Increased thirst and urination from hypokalaemia impairing renal concentrating ability
Headaches
Androgen-secreting adenoma (women):
Excess facial and body hair (hirsutism)
Acne
Irregular or absent periods
Deepening of the voice in severe cases
What causes adrenal adenomas?
The exact cause of most adrenal adenomas isn't fully understood, but a few factors are known to play a role:
Somatic mutations in genes that regulate adrenal cell growth and hormone production, including PRKACA (in cortisol-secreting adenomas), KCNJ5 (in aldosterone-secreting adenomas), and CTNNB1, can drive both the autonomous hormone output and the benign cell growth.
Age. Adrenal adenomas become significantly more common as people get older, with incidence rising from around 1% in the fourth decade of life to over 7% by the seventh.
Genetic syndromes. Multiple endocrine neoplasia type 1 (MEN1) and familial adenomatous polyposis (FAP) both raise the risk of developing an adrenal adenoma.
Obesity and metabolic syndrome. Both are linked to adrenal adenomas developing in the first place, and to autonomous cortisol secretion once one is present, which then worsens the metabolic syndrome further, a cycle that can reinforce itself over time.
How is an adrenal adenoma detected?
Adrenal adenomas are detected through abdominal imaging and characterised through hormonal blood testing. Both are essential.
Abdominal MRI Elfcare’s full-body MRI scans both adrenal glands to catch deep tissue abnormalities early. By measuring the tumour's size and picking up its fat content through specialised imaging (lipid-rich signals), the scan can usually identify the majority of benign adenomas, which tend to be lipid-rich. A minority are lipid-poor and don't show this signature; these get followed up with further imaging or monitoring to confirm they're benign. Size over 4 cm is one of several features, alongside imaging density, homogeneity, and growth over time, that prompts a more urgent evaluation.
Blood tests: Hormonal blood testing matters once an adrenal adenoma is identified, since imaging alone can't reliably tell functioning and non-functioning adenomas apart. Relevant markers in Elfcare's panel include:
Cortisol: measures your morning stress hormone levels to check for overproduction.
Aldosterone & renin ratio: screens for hormone-driven high blood pressure.
Potassium: low levels support a diagnosis of aldosterone excess when present, though around half of people with an aldosterone-secreting adenoma have normal potassium, so a normal result does not rule it out.
HbA1c and glucose: screens for hidden diabetes or insulin resistance, which excess cortisol can trigger.
Cholesterol panel (total, LDL, HDL, triglycerides): assesses overall cardiovascular risk, which is useful context alongside a functioning adenoma diagnosis, since conditions like Cushing's syndrome are associated with adverse lipid profiles over time.
Testosterone & DHEAS: measures male sex hormones to check for rare, masculinizing tumors.
ACTH: a specialized brain hormone marker used to confirm if your adrenal gland is malfunctioning completely on its own.
Why early detection matters
Autonomous cortisol secretion, even at levels too low to cause the classic features of Cushing's syndrome, still raises the risk of hypertension, type 2 diabetes, osteoporosis, and cardiovascular events on its own. Catching autonomous cortisol secretion early means surgical treatment (adrenalectomy) can resolve the hormone excess before these consequences build up, and in many cases reverse damage that's already occurred.
Primary hyperaldosteronism from an aldosterone-secreting adenoma is the most common cause of secondary hypertension, yet the majority of affected patients are treated for years with multiple antihypertensive medications without the underlying cause ever being identified. Surgical removal of the adenoma improves or normalises blood pressure in most patients, and a substantial proportion are able to stop or significantly reduce blood pressure medication altogether. Every year of undiagnosed functioning adrenal adenoma is a year of preventable cardiovascular, metabolic, and skeletal damage accumulating silently.
How Elfcare can help
Elfcare's full body MRI images both adrenal glands directly, identifying adenomas and checking their lipid content through chemical shift sequences, which picks up the lipid-rich majority of benign adenomas. The lipid-poor minority need further imaging or follow-up to characterise fully; Elfcare arranges this as part of further diagnostics when needed. Our blood panel covers cortisol, potassium, HbA1c, lipids, and sex hormones, giving the initial hormonal assessment needed to pick up the most common functioning adenoma subtypes.
When an adrenal adenoma on MRI lines up with blood results showing autonomous hormone production, that's about as clear and actionable as a health check finding gets: a treatable cause of hypertension, diabetes, osteoporosis, or cardiovascular disease that may have gone unexplained for years.
If our MRI or blood tests identify an adrenal adenoma or related findings, we take care of further diagnostics or refer you to the appropriate specialist.
Summary
Adrenal adenomas are the most common adrenal incidentaloma, showing up in roughly 3 to 7% of abdominal MRI scans. Most are non-functioning and just need imaging surveillance over time. A meaningful minority produce excess cortisol, aldosterone, or androgens, driving hypertension, metabolic syndrome, osteoporosis, and cardiovascular disease, all of which can often be reversed with surgery if caught early. Elfcare's full-body MRI images both adrenal glands directly and checks adenoma lipid content, and our blood panel covers cortisol, potassium, HbA1c, lipids, and sex hormones. Catching a functioning adrenal adenoma and treating it surgically before lasting cardiovascular and metabolic damage sets in protects long-term health, and for many people removes the need for lifelong medication altogether.
Last updated: 10 July 2026
Reviewed by: Specialist doctors from the quality team at Elfcare
FAQ
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An adrenal adenoma is a benign tumour arising from the adrenal cortex, the hormone-producing outer layer of the adrenal gland. It is the most common adrenal incidentaloma, found in approximately 3 to 7% of abdominal MRI scans. The majority are non-functioning and cause no hormonal consequences. A significant minority produce excess cortisol, aldosterone, or androgens, causing cardiovascular, metabolic, and skeletal consequences that are reversible with surgical treatment.
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Non-functioning adenomas cause no symptoms. Cortisol-secreting adenomas cause central weight gain, hypertension, diabetes, easy bruising, muscle weakness, and osteoporosis. Aldosterone-secreting adenomas cause resistant hypertension and low potassium causing weakness and fatigue. Subclinical autonomous cortisol secretion causes metabolic and cardiovascular consequences without the classic physical features of Cushing's syndrome, making blood testing essential even in apparently asymptomatic individuals.
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Somatic mutations in genes regulating adrenal cell proliferation and steroidogenesis are the primary cause in most cases. Age, obesity, metabolic syndrome, and genetic syndromes including MEN1 and Lynch syndrome are contributing risk factors. The majority of adrenal adenomas arise without an identifiable hereditary cause.
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Abdominal MRI identifies the adenoma and characterises its lipid content through chemical shift sequences, distinguishing it from malignant adrenal lesions. Hormonal blood testing assessing cortisol, aldosterone to renin ratio, and potassium determines whether the adenoma is functioning. Both imaging and hormonal assessment are essential after an adrenal mass is identified.
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Yes. Elfcare's full body MRI images both adrenal glands directly and characterises adenoma signal properties. Our blood panel covers cortisol, potassium, HbA1c, lipids, and sex hormones, providing the initial hormonal assessment. If an adrenal adenoma or related finding is identified, we take care of further diagnostics or refer you to the appropriate specialist.
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Yes. Non-functioning adenomas are managed with imaging surveillance to confirm stability. Functioning adenomas causing overt Cushing's syndrome, primary hyperaldosteronism, or virilisation are treated with laparoscopic adrenalectomy, which resolves hormonal excess and its consequences in the majority of cases. Subclinical autonomous cortisol secretion is managed with adrenalectomy in younger patients or those with significant metabolic consequences, or with medical management and cardiovascular risk reduction in older patients where surgical risk outweighs benefit. Early identification and treatment produces the best long-term metabolic and cardiovascular outcomes.