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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Case of the Week

Section Editors: Matylda Machnowska1 and Anvita Pauranik2
1University of Toronto, Toronto, Ontario, Canada
2BC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada

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Submit a Case Previous Cases ASPNR Pediatric Cases

September 14, 2009
  • Description
  • Diagnosis
  • Brain Teaser
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Multiple Nonsyndromic Schwannomas

  • Schwannomas are the most common intradural extramedullary tumors; meningioma is 2nd. Most schwannomas are intradural/extramedullary (70-75%), 15% are extra/intradural (dumbell-shaped), 15% are completely extradural and, rarely, they are intramedullary. They are more frequent in cervical and thoracic regions.
  • Hemorrhage and cystic degeneration are more common in schwannoma than neurofibroma; calcification is more common in meningioma.
  • On MRI, 75% are T2 hyperintense, 'target sign' is rare (high signal rim, low intensity center). They show intense enhancement after contrast, homogeneous or heterogeneous (peripheral).
  • Nonsyndromic lesions are usually solitary. Multiple can occur in patients with or without neurofibromatosis 2, schwanomatosis (no vestibular tumors) and Carney syndrome.
  • Schwannomas may be: typical, ancient, melanocytic, sarcomatous or Triton tumors.

Suggested Reading

Koeller KK, Rosenblum RS, Morrison AL. Neoplasms of the Spinal Cord and Filum Terminale: Radiologic-Pathologic Correlation.RadioGraphics 2000;20:1721-49.

Gebauer GP, Farjoodi P, Sciubba DM, et al. Magnetic Resonance Imaging of Spine Tumors: Classification, Differential Diagnosis, and Spectrum of Disease. JBJS 2008;90:146-62.

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American Journal of Neuroradiology: 46 (6)
American Journal of Neuroradiology
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