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Neurofibromas
may occur as a solitary nerve tumor,
usually noticed as a localised
mass under the skin. They differ
from schwannomas in that the neurofibroma
is intimately associated with the
nerve fibres running through it.
Consequently,
there will often be some form of neurologic
abnormality present in the case of
a neurofibroma; excision of the tumor,
if it involves a peripheral nerve,
may result in the loss of nerve function.
The figure below illustrates how the
tumor integrates with the nerve fibers:

A nerve may
also contain mulitple Neurofibromas,
in which case the surgeon has to consider
the possibility of a disease known
as Neurofibromatosis.
Neurofibromatosis,
a genetic disease associated with
the peripheral or central nervous
system, is characterized by multiple
tumors that have a tendency to be
malignant.
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