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Tumours
Meningioma
An in-depth, evidence-based guide to spinal meningiomas — usually benign tumours of the covering of the spinal cord — and how they are recognised, imaged and referred for specialist care.
A spinal meningioma is a tumour that grows from the meninges, the layers of tissue that cover and protect the spinal cord. It sits inside the dura but outside the cord itself, and as it enlarges it presses on the cord from the side or front. Spinal meningiomas are among the commonest tumours found in this location, are usually benign and slow-growing, and are more common in women and in the thoracic (mid-back) region. I want to be open about my role from the outset: I do not personally operate on primary spinal tumours such as this. My job is to recognise the problem, arrange the right imaging, and refer you promptly to a trusted colleague who specialises in spinal tumour surgery and performs it in high volume. This page explains what a spinal meningioma is and how it is assessed.
For information only — not medical advice. The content on this page is patient education to help you understand a condition or treatment. It is not a substitute for personalised assessment by a qualified clinician. Always consult your doctor or specialist about your own symptoms, diagnosis, and treatment decisions.
My role — recognising and referring, not operating
I think it is important to be straightforward. Although I am a spinal surgeon, primary tumours of the coverings of the spinal cord are a specialised field that I do not take on. I believe this surgery should be carried out by colleagues who do a high volume of it, because their experience translates into safer removal and better protection of the spinal cord. So when a meningioma is found, my role is to identify it, ensure the correct scans are done, and refer you without delay to an expert in spinal tumour surgery. What follows is written to help you understand the condition.
What a spinal meningioma is and how it causes symptoms
Because a meningioma grows slowly and presses on the cord gradually, symptoms usually develop over months and can be subtle at first. Common features include back pain, sometimes worse at night, followed by numbness or altered sensation, weakness or heaviness in the legs, problems with balance and walking, and, as compression advances, bladder or bowel symptoms. The pattern depends on where along the spine the tumour lies. Because the symptoms build up gradually, they are sometimes attributed to more common problems at first, which is one reason prompt, accurate assessment matters.
How it is diagnosed
The key investigation is an MRI scan with contrast, which shows the tumour, its exact position relative to the cord, and features that suggest it is a meningioma. This imaging is essential both for diagnosis and for the specialist surgeon to plan a safe removal. My part is to ensure this imaging is arranged and interpreted correctly, so that you reach the right specialist promptly and with the right information.
How it is treated — by a specialist colleague
The mainstay of treatment for a symptomatic or enlarging spinal meningioma is careful microsurgical removal by a spinal tumour specialist, using an operating microscope and, where appropriate, nerve monitoring to protect the cord. Because most spinal meningiomas are benign and well-defined, complete removal — including the small area of attachment — often gives an excellent and durable result, and the published evidence shows good neurological recovery and low recurrence when surgery is carried out by experienced, high-volume surgeons, even in older patients. The completeness of removal is described using the Simpson grading system, which the specialist will consider. Where surgery is needed, it belongs in expert hands, which is why I refer these cases on.
The information provided on this page is intended for educational purposes only and should not be considered personalised medical advice. Every patient is different, and treatment options, risks, expected recovery and outcomes depend upon an individual's diagnosis, general health and personal circumstances. Decisions regarding treatment should always be made following consultation with your treating spinal surgeon or healthcare professional.
Evidence & further reading
- —Setzer M, et al. Management of spinal meningiomas: surgical results and a review of the literature. Neurosurg Focus 2007. (PMID 17961038)
- —Gottfried ON, et al. Spinal meningiomas: surgical management and outcome. Neurosurg Focus 2003. (PMID 15669787)
- —Nakamura M, et al. Long-term surgical outcomes of spinal meningiomas. Spine 2012. (PMID 22146282)
- —Raco A, et al. Factors leading to a poor functional outcome in spinal meningioma surgery: 173 cases. Neurosurgery 2017. (PMID 28362922)
- —Sun SQ, et al. Simpson grade I–III resection of spinal atypical (WHO grade II) meningiomas. Neurosurgery 2015. (PMID 25774702)
- —Voldřich R, et al. Spinal meningiomas: is Simpson grade II resection radical enough? Acta Neurochir (Wien) 2020. (PMID 32166387)
- —Haddad AF, et al. Posterior-based resection of spinal meningiomas: 141 patients. J Neurosurg Spine 2023. (PMID 36152326)
- —Kilinc F, et al. Functional outcome and morbidity after microsurgical resection of spinal meningiomas. Neurosurg Focus 2021. (PMID 33932928)
- —Hohenberger C, et al. Functional outcome after surgical treatment of spinal meningioma. J Clin Neurosci 2020. (PMID 32409209)
- —Dang DD, et al. Spinal meningiomas: a comprehensive review and update. Cancers (Basel) 2024. (PMID 38611105)
- —Lenga P, et al. Spinal meningioma surgery in octogenarians: functional outcomes and complications. Medicina (Kaunas) 2022. (PMID 36295641)
- —Kwee LE, et al. Spinal meningiomas: treatment outcome and long-term follow-up. Clin Neurol Neurosurg 2020. (PMID 33096449)
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Every patient is different. The information on this page is a starting point — Mr Madi will tailor any plan to your specific imaging, symptoms and goals.
