Types of Spinal Tumours | Medibuddy
26th June 2023

Types of Spinal Tumours

Spinal tumours can be classified according to their location within the spine:

  • Intramedullary tumour – located inside the spinal cord (5% of spinal tumours; the majority are ependymomas and astrocytomas, but also include haemangioblastomas).
  • Intradural-extramedullary tumour – located inside the dura but outside of spinal cord. (40% of spinal tumours; these mostly consist of meningiomas and peripheral nerve sheath tumours).
  • Extradural tumour – located outside the dura, e.g. in the bones, discs and paraspinal soft tissues (55% of spinal tumours, the majority of which are metastases from other systemic cancers).

In MRCP 1, you are not expected to be able to differentiate the different subtypes, however, a brief knowledge of their aetiology is useful.

Ependymomas

Ependymomas are a subtype of gliomas. These cells line the fluid-filled ventricles in the brain and the centre of the spinal cord. Ependymomas are linked to the autosomal dominant disease, neurofibromatosis type 2 (NF2).

MRCP Part 1 - Ependymomas

Ependymomas

Image Source: Wikimedia Commons (2008). NF2 multiple intramedullary ependymomas 002, Licensed under a creative commons licence. Available for free at: https://commons.wikimedia.org/wiki/File:NF2_multiple_intramedullary_ependymomas_002.jpg (Accessed on: 30 January 2023).

Astrocytoma

Astrocytomas of the spinal cord are, in general, lower grade histologically than brain astrocytomas. They can be associated with neurofibromatosis type 1 (NF1). They are faster growing than ependymomas and the prognosis is worse. Surgery is the usual treatment choice, however, complete resection is rare due to their infiltrative nature. Radiotherapy and/or chemotherapy may also be used.

Haemangioblastomas

Haemangioblastomas are the third most common intramedullary spinal cord tumour, after ependymomas and astrocytomas. As with cerebellar haemangioblastomas, these are benign vascular tumours. They can be associated with Von Hippel-Lindau syndrome, as described earlier in this section. They are slow-growing and can be resected surgically. Endovascular embolisation may be required prior to surgical resection to minimise blood loss during surgery.

MRCP Part 1 - Haemangioblastoma

Haemangioblastoma.

Image Source: Wikimedia Commons (2007). Hippel Lindau, Licensed under a creative commons licence. Available for free at: https://commons.wikimedia.org/wiki/File:Hippel_Lindau.gif (Accessed on: 30 January 2023).

Meningiomas

A meningioma is a tumour that arises from the meninges. The meninges are membranes that cover and protect the brain and the spinal cord. There are three meningeal layers: dura mater; arachnoid mater; pia mater.

Risk factors include previous high dose ionising radiation and previous trauma. There is also an association with neurofibromatosis type 2.

MRCP Part 1 - Spinal meningioma on MRI

Spinal meningioma on MRI.

Image Source: Wikimedia Commons (2009). Meningeom im Spinalkanal MRT, Licensed under a creative commons licence. Available for free at: https://commons.wikimedia.org/wiki/File:Meningeom_im_Spinalkanal_MRT.jpg (Accessed on: 30 January 2023).

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