Meningioma
Last updated: 31 August 2026
Reviewed by: Specialist doctors from the Elfcare quality team
Meningiomas are tumours that develop from the protective membranes surrounding the brain and spinal cord. They are often slow-growing and may cause no symptoms at all, but depending on their size and location, they can sometimes lead to headaches, changes in vision, seizures, weakness, numbness, or changes in memory and personality.
Meningiomas are the most common intracranial tumour, accounting for approximately 37% of all primary brain tumours. The vast majority are benign and slow-growing, and many are discovered entirely incidentally on brain MRI performed for another reason. Understanding what a meningioma is, what it means for your health, and when it requires treatment is the most important step after receiving this finding.
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What is a meningioma?
A meningioma is a type of tumor that grows from the protective layers of tissue that wrap around your brain and spinal cord. They usually are very slow-growing, often changing by just a few millimeters a year. Instead of digging into the brain itself, they typically just press gently against the outside of it as they grow.
Meningiomas are classified by WHO grade:
Grade 1 (benign): this accounts for about 8 out of 10 cases. These are non-cancerous, grow very slowly, and often stay the exact same size for years or even decades without needing any treatment at all.
Grade 2 (atypical): making up about 15% to 20% of cases, these grow a bit faster and are more likely to return if removed, sometimes requiring extra treatment like radiation after surgery.
Grade 3 (malignant): this type is very rare, making up less than 3% of cases. They behave aggressively, can grow into the nearby brain tissue, and require immediate medical attention.
Where the tumor is located inside your head depends entirely on luck, and its position is what determines whether it causes symptoms (like headaches or vision changes) and how easy it is for a doctor to reach.
Symptoms of a meningioma
Many meningiomas cause no symptoms and are discovered incidentally on MRI. When symptoms occur they develop gradually and reflect the size and location of the tumour and its effect on adjacent structures:
Headaches, often progressive and worse in the morning or when lying down
Seizures, particularly in tumours involving the cerebral cortex
Visual disturbances including blurred vision, double vision, or visual field loss from tumours near the optic pathways or cavernous sinus
Weakness or numbness on one side of the body from tumours compressing the motor or sensory cortex
Speech or language difficulties from dominant hemisphere tumours
Personality or cognitive changes from frontal lobe compression
Hearing loss or tinnitus from posterior fossa or cerebellopontine angle meningiomas
Spinal cord or nerve root compression symptoms from spinal meningiomas
What causes meningioma?
The exact cause is not fully understood in most cases. Contributing factors include:
Prior radiation to the head: the most clearly established environmental cause. Radiation-induced meningiomas typically develop 15 to 20 years after exposure and tend to be more aggressive than sporadic tumours.
Female sex and hormonal factors: meningiomas are approximately twice as common in women as in men and express progesterone and estrogen receptors. They frequently grow during pregnancy and may enlarge with hormonal therapies.
Genetic conditions: neurofibromatosis type 2 is the most important genetic cause, associated with multiple meningiomas alongside schwannomas and other CNS tumours. Other genetic mutations including in NF2, TRAF7, AKT1, and SMO genes are identified in sporadic meningiomas.
Age: meningiomas are rare in children and adolescents, with incidence rising progressively from the fourth decade onwards.
Obesity: it is associated with modestly increased meningioma risk through mechanisms that are not fully understood.
How is a meningioma detected?
Meningiomas are detected through brain or spinal MRI, with blood tests playing a supporting role in relevant hormonal and systemic contexts.
Brain and spinal MRI Elfcare’s full-body MRI easily spots meningiomas, which are common, usually harmless lumps growing on the protective lining outside the brain. The scan usually allows doctors to identify a meningioma with high confidence based on its characteristic appearance, while also showing its size and location. Finding one unexpectedly simply allows you to start a safe plan to monitor it over time, typically avoiding any immediate treatment.
Blood tests cannot detect meningiomas but provide relevant hormonal and systemic context. Relevant markers in Elfcare's panel include:
Estradiol and progesterone: assess hormonal context relevant to hormone receptor-positive meningiomas, which may be influenced by hormonal status and HRT use
LH and FSH: provide menopausal status context relevant to hormonal influence on meningioma behaviour
CRP: reflects systemic inflammation relevant to post-surgical assessment and general health context
Full blood count: provides baseline systemic health assessment relevant to surgical planning if intervention is being considered
HbA1c and glucose: metabolic health assessment relevant to surgical risk and overall health context
Why early detection matters
The vast majority of meningiomas grow slowly, and for small asymptomatic tumours identified early, the management approach is typically surveillance with serial MRI rather than immediate surgery. This approach, only possible when the tumour is identified before it causes significant neurological compromise, avoids the risks of surgery while monitoring for any clinically significant growth. When intervention eventually becomes necessary, surgery on a small meningioma that has been monitored and planned electively carries significantly lower risk than emergency surgery on a large tumour causing acute neurological deterioration. For the smaller proportion of higher-grade meningiomas, early identification before significant brain invasion or oedema has occurred allows for surgical removal with cleaner margins and better long-term outcomes.
How Elfcare can help
Elfcare's full body MRI includes comprehensive brain imaging that can identify meningiomas and characterise their size and location. Meningioma is one of the most commonly identified and clinically meaningful incidental findings on brain MRI, providing a structural diagnosis that changes how symptoms are understood and managed, or providing reassurance and a monitoring plan for an entirely asymptomatic finding.
Our blood panel covers hormonal markers relevant to meningioma behaviour and baseline systemic health relevant to management planning.
If our MRI identifies a meningioma, we take care of further diagnostics or refer you to the appropriate specialist.
Summary
Meningiomas are the most common primary intracranial tumour, arising from the protective membranes of the brain and spinal cord. The vast majority are benign and slow-growing, and many are discovered incidentally on brain MRI before causing any symptoms. Elfcare's full body MRI can identify features that are highly suggestive of a meningioma and characterise its size and location, although definitive diagnosis occasionally requires tissue analysis after surgery. Early identification allows appropriate monitoring or treatment planning before significant neurological symptoms develop.
Last updated: 31 August 2026
Reviewed by: Specialist doctors from the quality team at Elfcare
FAQ
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A meningioma is a tumour arising from the meninges, the protective membranes surrounding the brain and spinal cord. It is the most common primary intracranial tumour, accounting for approximately 37% of all brain tumours. The vast majority are benign and slow-growing. They compress rather than invade adjacent brain tissue and are frequently discovered incidentally on brain MRI with no preceding symptoms.
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Many meningiomas cause no symptoms. When symptoms occur they depend on location and include progressive headaches, seizures, visual disturbances, one-sided weakness or numbness, speech difficulties, personality changes, and hearing loss. Symptoms develop gradually as the tumour enlarges and compresses adjacent brain structures.
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Prior radiation to the head is the most clearly established environmental cause. Female sex and hormonal factors significantly influence risk and tumour behaviour. Neurofibromatosis type 2 is the most important genetic cause. Age, with incidence rising progressively from the fourth decade, and obesity are additional contributing factors.
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Brain MRI is the primary detection tool, identifying meningiomas as well-defined extra-axial masses with characteristic features including a dural tail sign that distinguish them from other intracranial tumours with high confidence. Size, location, brain compression, and oedema are all assessed in a single examination.
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Yes. Elfcare's full body MRI includes comprehensive brain imaging as standard, directly identifying and characterising meningiomas. Meningioma is one of the most commonly identified incidental findings on brain MRI. If a meningioma is identified, we take care of further diagnostics or refer you to the appropriate specialist.
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Yes. Small asymptomatic meningiomas are managed with serial MRI surveillance, with intervention reserved for evidence of growth or symptom development. Symptomatic or growing meningiomas are treated with surgical removal, which is curative for completely excised grade 1 tumours. Stereotactic radiosurgery is an effective alternative for small or surgically inaccessible tumours. Grade 2 and 3 meningiomas require surgery followed by radiotherapy. Early identification of a meningioma before neurological compromise has developed provides the most favourable conditions for planned, low-risk treatment with excellent long-term outcomes.