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Neurofibromatosis, Type 2
Acoustic Schwannoma. In NF2, patients develop bilateral acoustic schwannomas, along with spinal cord ependymomas, and multiple meningiomas.

Neurofibromatosis, Type 2

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Genetics
Incidence of ~ 1/30,000 (think: one-tenth as common as NF-1*)
  • 50% of cases are Autosomal Dominant inherited, the remainder are spontaneous.
  • NF2 gene mutation is on chromosome 22 and affects a cytoskeleton protein, merlin, which regulates receptor signaling.
    • Mnemonic: NF2 mutation is on chromosome22.
Tumors
  • Bilateral acoustic schwannomas (8th nerve tumors)
    • Bilateral acoustic schwannomas are diagnostic of NF-2.
  • Meningiomas
    • Multiple meningiomas are characteristic of NF-2.
    • By the 7th decade, > 75% of patients will have a meningioma.
  • Ependymomas of the spinal cord
    • The most common adult-onset intramedullary spinal cord tumor is ependymoma.
Nonneoplastic lesions
  • Nodular ingrowth into the spinal cord (schwannosis)
  • Meningeal cell and blood vessel proliferation into the brain (meingoangiomatosis)
Glial hamartia (microscopic nodular collections of glial cells within the cerebral cortex), especially important cause of seizures*
  • Juvenile cataracts
References
Image Reference
  • Acoustic Schwannoma.
    • Image from MBq, Selbsterstellt, Germany