A Rare Finding of Schwannoma of the Vidian Canal: A Case Report
Lin, Giant C.
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CitationYamasaki, Alisa, Ahmad R. Sedaghat, Giant C. Lin, William T. Curry, Helen A. Shih, and Stacey T. Gray. 2015. “A Rare Finding of Schwannoma of the Vidian Canal: A Case Report.” Journal of Neurological Surgery Reports 76 (1): e48-e51. doi:10.1055/s-0034-1544112. http://dx.doi.org/10.1055/s-0034-1544112.
AbstractBackground: Schwannomas of the vidian canal are an extremely rare type of intracranial tumor that can have variable clinical presentations including headache, facial pain, facial muscle paralysis, decreased lacrimation, or nasal dryness. We present an atypical case of an incidentally identified asymptomatic vidian canal schwannoma. Case Description A 49-year-old woman with a history of multiple sclerosis presented for routine surveillance magnetic resonance imaging that detected an ovoid mass originating in the vidian canal. Given the unusual location of the lesion, an endoscopic endonasal biopsy was performed and confirmed the diagnosis of a vidian canal schwannoma, for which the patient chose to receive fractionated radiation therapy. Conclusion: When a vidian canal tumor is identified, endoscopic endonasal biopsy can be used to confirm the diagnosis before pursuing either surgical or radiotherapy treatment. In particular, fractionated radiation therapy offers a radiobiologically safe means of delivering radiation when there is concern for late radiation-related side effects following treatment completion.
Citable link to this pagehttp://nrs.harvard.edu/urn-3:HUL.InstRepos:21462107
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