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  • Meningioma in Neurofibromatosis Type II

    Final Number:
    1340

    Authors:
    Gregory P. Lekovic MD, PhD; Marc S. Schwartz MD

    Study Design:
    Other

    Subject Category:

    Meeting: Congress of Neurological Surgeons 2012 Annual Meeting

    Introduction: Meningioma constitutes a significant disease burden for patients with NF2. We present our experience with intracranial meningioma in NF2 with regard to indications for treatment, goals of surgery, and outcome.

    Methods: The charts of all patients followed by an interdisciplinary NF2 tumor board at the House Research Institute between 2005 and 2010 were retrospectively reviewed; patients undergoing craniotomy or stereotactic radiosurgery (SRS) for the primary indication of meningioma by the authors were included in the study population. Patients operated on for other indications (e.g. vestibular schwannoma) in whom meningioma was coincidentally removed were excluded.

    Results: 144 patients were identified, of whom 11 (4M:7F; age 19-56) underwent a total of 22 procedures (18 craniotomy and 4 SRS) for 18 meningiomas. Indications included symptomatic growing tumor (n=11) and rapid tumor growth (n=7). Locations included skull base (n=6); falx (n=4); tentorium (n=3); pineal (n=2); convexity (n=2), and intraventricular (n=1). Extent of resection was gross total (n=12); subtotal (n=5), biopsy (n=1). Follow up was 6-108 months. Indications for SRS included unresectable tumor (n=1), recurrence (n=2), and medical contraindication to surgery (n=1). All tumors were WHO grade I except one WHO grade II tumor that recurred after GTR requiring both re-resection and SRS. There was one other recurrence of sub-totally resected tumor. Morbidity included brachial plexopathy (n=1) and hydrocephalus (n=2). There were no mortalities.

    Conclusions: The indications, techniques and goals of surgery are different in the NF2 population from sporadic menginioma. We are unable to verify a high incidence of atypical meningioma in the NF2 population as has been recently reported elsewhere. In spite of the high prevalence of meningioma in NF2, we conclude that most meningiomas in NF2 can be followed safely without intervention.

    Patient Care: This research aids in the understanding of the natural history and management of meningiomas in NF2

    Learning Objectives: By the conclusion of this session, participants should be able to: 1) understand the indications for treatment of intracranial meningioma in the NF2 population as distinct from sporadic meningioma; 2) discuss the evidence regarding the incidence of atypical meningioma in the NF2 population; 3) describe the natural history of meningioma in the NF2 population.

    References:

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