• Neurosurgery · Apr 2024

    Lower Cranial Nerve Schwannomas: Cohort Study and Systematic Review.

    • Lucas P Carlstrom, Megan M J Bauman, Soliman Oushy, Avital Perry, Paul D Brown, Maria Peris-Celda, Jamie J Van Gompel, Christopher S Graffeo, and Michael J Link.
    • Department of Neurosurgery, Mayo Clinic, Rochester , Minnesota , USA.
    • Neurosurgery. 2024 Apr 1; 94 (4): 745755745-755.

    Background And ObjectivesSchwannomas originating from the lower cranial nerves (LCNS) are rare and pose a significant surgical challenge. Resection is the mainstay treatment; however, risk of treatment morbidity is considerable, and the available literature regarding differential treatment outcomes in this vulnerable population is sparse.MethodsA single-institution cohort study and systematic literature review of LCNS were performed.ResultsFifty-eight patients were included: 34 underwent surgical resection and 24 underwent stereotactic radiosurgery (SRS). The median age at diagnosis was 48 years (range 17-74). Presenting symptoms were dysphagia (63%), dysarthria/hypophonia (47%), imbalance (33%), and hearing loss/tinnitus (30%). Tumor size was associated with surgical resection, as compared with initial SRS (4.1 cm vs 1.5 cm, P = .0001). Gross total resection was obtained in 52%, with tumor remnants predominantly localized to the jugular foramen (62%). Post-treatment worsening of symptoms occurred in 68% of surgical and 29% of SRS patients ( P = .003). Postoperative symptoms were mostly commonly hypophonia/hoarseness (63%) and dysphagia (59%). Seven patients (29%) had new neurological issues after SRS treatment, but symptoms were overall milder. The median follow-up was 60 months (range 12-252); 98% demonstrated meaningful clinical improvement. Eighteen surgical patients (53%) underwent adjuvant radiation at a median of 5 months after resection (range 2-32). At follow-up, tumor control was 97% in the surgical cohort and 96% among SRS patients.ConclusionAlthough LCNS resection is potentially morbid, most postoperative deficits are transient, and patients achieve excellent tumor control-particularly when paired with adjuvant SRS. For minimally symptomatic patients undergoing surgical intervention, we advise maximally safe resection with intracapsular dissection to preserve nerve integrity where possible. For residual or as a primary treatment modality, SRS is associated with low morbidity and high rates of long-term tumor control.Copyright © Congress of Neurological Surgeons 2023. All rights reserved.

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