Intracisternal cranial root accessory nerve schwannoma associated with recurrent laryngeal neuropathy

Sung Won Jin, Kyung-Jae Park, D. H. Dong-Hyuk, Shin-Hyuk Kang

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1 Citation (Scopus)


Intracisternal accessory nerve schwannomas are very rare; only 18 cases have been reported in the literature. In the majority of cases, the tumor origin was the spinal root of the accessory nerve and the tumors usually presented with symptoms and signs of intracranial hypertension, cerebellar ataxia, and myelopathy. Here, we report a unique case of an intracisternal schwannoma arising from the cranial root of the accessory nerve in a 58-year-old woman. The patient presented with the atypical symptom of hoarseness associated with recurrent laryngeal neuropathy which is noted by needle electromyography, and mild hypesthesia on the left side of her body. The tumor was completely removed with sacrifice of the originating nerve rootlet, but no additional neurological deficits. In this report, we describe the anatomical basis for the patient’s unusual clinical symptoms and discuss the feasibility and safety of sacrificing the cranial rootlet of the accessory nerve in an effort to achieve total tumor resection. To our knowledge, this is the first case of schwannoma originating from the cranial root of the accessory nerve that has been associated with the symptoms of recurrent laryngeal neuropathy.

Original languageEnglish
Pages (from-to)152-156
Number of pages5
JournalJournal of Korean Neurosurgical Society
Issue number2
Publication statusPublished - 2014 Jan 1



  • Accessory nerve
  • Intracisternal
  • Recurrent laryngeal neuropathy
  • Schwannoma

ASJC Scopus subject areas

  • Surgery
  • Neuroscience(all)
  • Clinical Neurology

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