Lower Cranial Nerve Schwannomas: Cohort Study and Systematic Review

Author:

Carlstrom Lucas P.1ORCID,Bauman Megan M. J.1,Oushy Soliman1,Perry Avital2,Brown Paul D.3,Peris-Celda Maria14,Van Gompel Jamie J.14,Graffeo Christopher S.5,Link Michael J.14

Affiliation:

1. Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA;

2. Department of Neurosurgery, Sheba Medical Center, Tel Aviv, Israel;

3. Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota, USA;

4. Department of Otolaryngology, Mayo Clinic, Rochester, Minnesota, USA;

5. Department of Neurosurgery, University of Oklahoma, Oklahoma City, Oklahoma, USA

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Surgery

Reference62 articles.

1. Jugular foramen neuromas: a review of 14 cases;Tan;Surg Neurol.,1990

2. Surgical treatment of jugular foramen schwannomas;Samii;J Neurosurg.,1995

3. Microsurgical management of hypoglossal schwannomas over 3 decades: a modified grading scale to guide surgical approach;Nonaka;Neurosurgery.,2011

4. Surgical treatment of jugular foramen schwannoma: surgical treatment based on a new classification;Samii;Neurosurgery.,2015

5. Jugular foramen schwannoma: analysis on its origin and location;Song;Otol Neurotol.,2008

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