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Lower Cranial Nerve Schwannomas: Cohort Study and Systematic Review.
Carlstrom, Lucas P; Bauman, Megan M J; Oushy, Soliman; Perry, Avital; Brown, Paul D; Peris-Celda, Maria; Van Gompel, Jamie J; Graffeo, Christopher S; Link, Michael J.
Afiliação
  • Carlstrom LP; Department of Neurosurgery, Mayo Clinic, Rochester , Minnesota , USA.
  • Bauman MMJ; Department of Neurosurgery, Mayo Clinic, Rochester , Minnesota , USA.
  • Oushy S; Department of Neurosurgery, Mayo Clinic, Rochester , Minnesota , USA.
  • Perry A; Department of Neurosurgery, Sheba Medical Center, Tel Aviv , Israel.
  • Brown PD; Department of Radiation Oncology, Mayo Clinic, Rochester , Minnesota , USA.
  • Peris-Celda M; Department of Neurosurgery, Mayo Clinic, Rochester , Minnesota , USA.
  • Van Gompel JJ; Department of Otolaryngology, Mayo Clinic, Rochester , Minnesota , USA.
  • Graffeo CS; Department of Neurosurgery, Mayo Clinic, Rochester , Minnesota , USA.
  • Link MJ; Department of Otolaryngology, Mayo Clinic, Rochester , Minnesota , USA.
Neurosurgery ; 94(4): 745-755, 2024 Apr 01.
Article em En | MEDLINE | ID: mdl-37874134
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Schwannomas 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.

METHODS:

A single-institution cohort study and systematic literature review of LCNS were performed.

RESULTS:

Fifty-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.

CONCLUSION:

Although 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos de Deglutição / Radiocirurgia / Neurilemoma Tipo de estudo: Systematic_reviews Limite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Revista: Neurosurgery Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos de Deglutição / Radiocirurgia / Neurilemoma Tipo de estudo: Systematic_reviews Limite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Revista: Neurosurgery Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos