Intracavernous granular cell tumor

Surg Neurol. 2004 Apr;61(4):384-90; discussion 390. doi: 10.1016/S0090-3019(03)00291-X.

Abstract

Background: Granular cell tumors in the central nervous system are quite rare. To date, only 6 cases of granular cell tumor arising from cranial nerves have been reported in the literature. To the best of our knowledge, we present the first case of a predominant intracavernous granular-cell tumor arising from oculomotor nerve.

Case presentation: A 42-year-old man presented with third-nerve paresis and decreased visual acuity on the left side. Magnetic resonance imaging showed a mainly intracavernous mass partially extending to the superior orbital fissure and entrance of the optic canal. Using a pterional craniotomy, the tumor was removed from within the cavernous sinus via combined superior and lateral intradural approach, and optic nerve was also decompressed. Histologically, the tumor was diagnosed as a granular cell tumor.

Conclusions: Although it is quite rare, granular cell tumor should be included into the differential diagnosis of intracavernous masses because surgical treatment is curative.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Brain Neoplasms / complications
  • Brain Neoplasms / pathology*
  • Brain Neoplasms / surgery
  • Cavernous Sinus / pathology*
  • Cavernous Sinus / surgery
  • Craniotomy
  • Diagnosis, Differential
  • Granular Cell Tumor / complications
  • Granular Cell Tumor / pathology*
  • Granular Cell Tumor / surgery
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Oculomotor Nerve Diseases / etiology