Interactive Transcript
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Although we described chronic inflammatory demyelinating
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polyradiculoneuropathy and the hypertrophic motor
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sensory neuropathy syndromes when we were talking
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about intradural extramedullary lesions,
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the truth is that these may be purely extradural
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diseases of the nerve roots.
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CIDP is an acquired disorder usually thought to be an
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autoimmune disorder in which the patients present
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with proximal weakness and paresthesias,
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they may affect the cranial nerves or the peripheral
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nerves, and it is usually a bilateral and symmetric
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process. When it's unilateral or asymmetric, it may be
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called MMN, which is Multifocal Motor Neuropathy.
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Here we have examples of a patient who has enlargement
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of the nerve roots which is predominantly in
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the extradural compartment. As you can see,
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this is going through the anterior scaling,
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middle scaling junction involving the brachial plexus.
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And this is on T2-weighted scan,
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T1-weighted scan, and you see that there are enlarged
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neuroforamina, as well as the involvement of the
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nerves as they go into the brachial plexus.
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So this is called CIDP and it is, again, an autoimmune
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disorder which is often treated with immunosuppressive
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medications and definitively with plasmapheresis.
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In the differential diagnosis with CIDP are the
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hereditary motor and sensory neuropathy
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syndrome, such as your Charcot-Marie-Tooth disease and Dejerine–Sottas disease,
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which may be purely extradural.
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Also in the differential diagnosis, one may find some of the mucopolysaccharidoses
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which also may be associated with enlarged
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nerve roots, as well as dural thickening,
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most commonly at the foramen magnum
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and C1-C2 junction.
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So these are causes of enlarged extradural nerve roots.
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