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Home  /  Treatments  /  Neurosurgery  /  Meningioma

Meningioma

A tumour arising from the membranes covering the brain rather than from brain tissue itself. Most are benign and slow-growing, and a substantial proportion never need any treatment.

Meningioma is the brain tumour most often overtreated. Small ones found incidentally on a scan performed for something else can frequently be watched for years, and knowing that before you agree to an operation is worth a great deal.

Most are
Benign, grade one
Slow-growing, and often need no treatment
Frequently
Watched, not operated
Small incidental tumours are monitored
Complete removal
Often curative
Where the tumour is accessible
Time in India
3 to 5 weeks
Less for radiosurgery
The condition

What a meningioma is

Meningiomas arise from the arachnoid layer of the meninges — the membranes wrapping the brain — and grow inward, pushing the brain aside rather than infiltrating it. That single characteristic is what makes them so different from gliomas: there is usually a plane between tumour and brain, and complete removal is frequently achievable.

They are graded one to three. The great majority are grade one, benign and slow-growing. Grade two atypical meningiomas recur more often, and grade three anaplastic meningiomas are uncommon and behave aggressively.

They are considerably more common in women, and a proportion enlarge during pregnancy. Previous radiation to the head is a recognised risk factor, and multiple meningiomas can occur in neurofibromatosis type 2.

Because MRI is now performed frequently for headaches, dizziness and after minor head injuries, a great many meningiomas are found by accident in people with no symptoms attributable to them. Deciding what to do about those is the central question this page addresses.

Symptoms

Symptoms and warning signs

Common symptoms
  • Often none at all — found incidentally on a scan
  • Headache, gradually increasing over months
  • A first seizure
  • Progressive weakness or numbness on one side
  • Visual disturbance or loss of part of the visual field
  • Loss of smell, with tumours at the front of the skull base
  • Personality change or apathy, with frontal tumours
Warning signs of an emergency
  • Severe headache with vomiting and drowsiness
  • Rapidly worsening weakness or speech difficulty
  • A seizure lasting more than five minutes
  • Sudden visual loss
  • New confusion or reduced consciousness
  • Rapid enlargement on repeat imaging

A small meningioma found by accident often needs watching, not surgery

Many meningiomas are discovered on scans done for headaches, dizziness or minor head injury, in people whose symptoms are not caused by the tumour at all. For a small, calcified, slow-growing tumour away from critical structures, in an older patient, the correct management is frequently a repeat scan in six to twelve months rather than an operation. Brain surgery carries real risk, and a tumour that will never cause trouble should not be the reason to accept it. If surgery has been recommended for a small incidental meningioma, ask what the growth rate is and what would happen if you waited.

Diagnosis

How it is diagnosed

MRI usually makes the diagnosis without any need for tissue.

Initial tests

  • MRI with contrast — meningiomas have a characteristic appearance with a dural tail, usually diagnostic
  • CT scan — shows calcification and any involvement or thickening of the adjacent skull
  • Serial imaging — comparing scans over time gives the growth rate, which is often the deciding factor
  • Visual field testing — where the tumour is near the optic pathways

The deciding tests

  • MR or CT angiography — shows the tumour's blood supply and its relationship to major vessels and sinuses
  • Preoperative embolisation — blocking feeding vessels before surgery to reduce bleeding in large tumours
  • Hearing tests — for tumours near the hearing apparatus
  • Endocrine assessment — where the tumour lies near the pituitary region

If you have two scans, send both

The growth rate is often more important than the size. A meningioma unchanged over two years behaves very differently from one that has grown noticeably in six months, and that difference frequently decides between observation and surgery. Send every scan you have with its date, not only the most recent one.

Options

Treatment options

Doing nothing is a legitimate and frequently correct choice.

Option one

Observation with serial imaging

Repeat MRI at intervals — typically six to twelve months initially, then less often if stable — with treatment only if the tumour grows or begins to cause symptoms. For small, asymptomatic, calcified tumours, particularly in older patients, this is the evidence-based approach and avoids the risks of surgery entirely.

Usually appropriate whenA small tumour causing no symptoms, in a location where growth would be detected before it caused harm.
Option two

Surgical removal

The tumour is removed along with its dural attachment where possible. Complete removal of a grade one meningioma is frequently curative, and the extent of removal — graded on the Simpson scale — predicts the chance of recurrence. Accessibility varies enormously: a convexity meningioma is straightforward, one at the skull base wrapped around vessels and nerves is not.

Usually appropriate whenSymptomatic tumours, growing tumours, or large tumours compressing brain tissue.
Option three

Stereotactic radiosurgery

Focused radiation delivered in one or a few sessions with no incision. It controls growth in the large majority of small to moderate meningiomas and is particularly useful for tumours at the skull base where surgery carries higher risk. It does not remove the tumour — it stops it growing.

Usually appropriate whenSmall to moderate tumours, difficult surgical locations, residual tumour after surgery, or patients unfit for an operation.
Option four

Surgery followed by radiation

For atypical or anaplastic meningiomas, and for tumours where complete removal was not possible, radiotherapy after surgery reduces the chance of recurrence. Higher-grade meningiomas need closer long-term surveillance regardless of treatment.

Usually appropriate whenGrade two or three tumours, or incomplete removal of a grade one tumour in a difficult location.
The decision

How the choice is made

Symptoms and growth rate

A tumour causing symptoms or demonstrably growing needs treatment. One doing neither often does not.

Location and accessibility

Convexity tumours are removable with low risk. Skull base tumours involving vessels and cranial nerves carry considerably more, and radiosurgery may be the better option.

Your age and general health

An eighty-year-old with a small stable meningioma is very unlikely to be harmed by it. A forty-year-old with the same tumour has decades ahead and a different calculation.

If your scan shows a small stable meningioma and you have no symptoms attributable to it, we will tell you that observation is reasonable — even though that means no case for us.

Urgency

How urgent is your case

Usually safe to plan travel
  • Incidental finding, no symptoms
  • Stable on serial imaging
  • Symptoms stable and controlled
  • Planning elective surgery or radiosurgery
Needs local assessment before travel
  • Drowsiness or reduced consciousness
  • Severe headache with vomiting
  • Rapidly progressive weakness
  • Uncontrolled seizures
  • Sudden visual deterioration

We will tell you which column you are in

Most meningiomas allow ample time to plan carefully. A large tumour with surrounding swelling and drowsiness is different and needs local treatment first.

Next step

What to send us

Photographs taken on your phone are fine. Reports in Arabic, Russian or Bengali are fine — we translate them ourselves.

Most useful

  • MRI with contrast — report and images
  • Every previous scan, with dates, so growth can be assessed
  • CT scan if performed
  • A description of any symptoms and when they began

Also helpful

  • Visual field test results if done
  • Angiography if performed
  • Your age and other medical conditions
  • Any previous radiation to the head
Questions

Questions patients ask

Possibly not. Many meningiomas, particularly small ones found incidentally in people without symptoms, are best watched with repeat scans. Surgery is indicated where the tumour causes symptoms, is growing, or is large enough to compress brain tissue. Ask what your growth rate is before agreeing to an operation.

The great majority are benign — grade one — and are not cancer in the usual sense. They do not spread elsewhere in the body. A minority are grade two, which recur more readily, and a small number are grade three and behave aggressively. The grade is determined on tissue after surgery, not on the scan.

Highly focused radiation delivered in one or a few sessions with no incision and usually no hospital stay. It controls growth in most small to moderate meningiomas and is especially valuable at the skull base where open surgery is riskier. It does not shrink the tumour quickly — it stops it growing, and the effect is judged over months and years.

It depends on the grade and on how completely it was removed, including its dural attachment. A completely removed grade one meningioma often does not recur. Incomplete removal, or a higher grade, carries a meaningful recurrence rate and requires continued surveillance scanning for years.

It can. Meningiomas are more common in women and some enlarge during pregnancy, occasionally causing symptoms that settle afterwards. If you have a known meningioma and are planning pregnancy, it is worth discussing beforehand so that monitoring can be arranged.

Not more dangerous in itself, but harder to remove. Skull base meningiomas can wrap around arteries and cranial nerves, and attempting complete removal may risk stroke or nerve injury. In these cases a planned partial removal followed by radiosurgery to the remnant often gives a better overall result than aggressive resection.

Contact

Send us your reports

Send the MRI and every earlier scan you have, with dates. Growth rate over time often decides whether you need an operation at all.

Your reports go directly to our medical team. We do not share your records with hospitals until you tell us to.

WhatsApp +91 83035 86344  ·  Phone +91 83035 86344  ·  Email tibhind@gmail.com

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