J Neurol Surg B Skull Base 2025; 86(S 01): S1-S576
DOI: 10.1055/s-0045-1803641
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Intracranial Vagal Nerve Schwannoma—Presentation, Surgical Options, and Outcomes

M. Salman Ali
1   Medical College of Georgia at Augusta University, Augusta, Georgia, United States
,
Fernando Vale
1   Medical College of Georgia at Augusta University, Augusta, Georgia, United States
› Author Affiliations
 
 

    Introduction: Vagal nerve schwannomas are rare types of schwannomas. Majority of these tumors present as masses in the neck. Intracranial vagal nerve schwannomas are even rare.

    Materials and Methods: A retrospective analysis was performed, and a single case of intracranial vagal nerve schwannoma was identified.

    Results: Patient was a 33-year-old female, single mother of 5 years. She presented with dizziness and gait imbalance. She was diagnosed with a large posterior fossa mass extending into the jugular foramen displacing internal carotid artery and jugular vein, anteriorly and posteriorly, respectively. There was significant mass effect from posterior fossa mass. Surgical options including retrosigmoid craniotomy alone with posterior mass resection versus more aggressive petrooccipital transsigmoid (POTS) approach to attempt gross total resection. Her vocal cord analysis and swallow study was normal. After lengthy discussion with the patient and her current social situation, it was decided to proceed with retrosigmoid craniotomy with endoscopic assistance. Posterior fossa tumor was resected which was extending up to tentorium. Using 30-degree endoscope tumor was chased into the jugular foramen up to carotid artery. She tolerated the procedure well with mild facial nerve weakness (HB II). She was evaluated by physical therapy and discharged home on post-operative day 2. On follow-up appointment in 6 weeks, her facial weakness had improved to HB I. She is being closely monitored for tumor progression.

    Conclusion: Patients with intact cranial nerves present a challenge in decision making. Patient’s young age puts her at greater risk for tumor recurrence. At the same time, a single mother of 5 kids, youngest being 5 years old, presents another challenge. Aggressive resection carries a significant complication risk which could prevent the patient from taking care of her young kids. Our plan is to proceed with radiation and closely monitor cranial nerve function. If the tumor progresses after radiation treatment, considering her young, we will proceed with more aggressive surgical resection. As for now, she remains asymptomatic.

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    No conflict of interest has been declared by the author(s).

    Publication History

    Article published online:
    07 February 2025

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