Neurofibromatosis type 2
ICD-10 Q85.0 · ICD-11 LD2D.11

Treatment of Neurofibromatosis Type 2 with Intramedullary Spinal Tumor (Ependymoma)

Clinical Scenario

This protocol addresses Neurofibromatosis type 2 (NF2) in a patient presenting with an intramedullary spinal tumor — specifically an ependymoma arising within the spinal cord. This tumour type carries distinct management considerations within the NF2 context.

Specific Situation

Intramedullary spinal tumors, including ependymomas, arise within the substance of the spinal cord and require careful evaluation of local treatment modalities. Their management in NF2 follows specific priorities that differ from other tumour locations.

Treatment Approach (Partial)

Surgical intervention is the primary modality considered for intramedullary spinal ependymoma in this setting.

The complete protocol covers additional options and the specific conditions under which each applies — access it below.

Instant Access to Structured Evidence-Based Regimens

References

Intramedullary spinal tumors, like ependymomas, generally prefer surgical resection over radiotherapy.

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