Interactive Transcript
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Hi, it's Dave Yousem from Johns Hopkins University
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School of Medicine. Here to talk to you today
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about intradural intramedullary spinal lesions.
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Classically, when we think about spinal lesions,
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we separate them into three different
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categories, intradural intramedullary lesions,
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intradural extramedullary lesions, and extradural lesions.
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The extradural lesions, by and large,
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are most commonly secondary to degenerative
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disease and this includes degenerative disc disease
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and osteophytes and ligamentum flavum thickening,
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as well as facet joint disease.
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These are lesions which compress the spinal
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cord and the CSF from outside the thecal sac.
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Contrast that with the intradural diseases.
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These are diseases that compress the
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cord within the thecal sac.
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However, the extramedullary lesions are ones that are
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outside the spinal cord, demonstrated here,
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whereas the intradural intramedullary lesions are
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the lesions that are intrinsic to the spinal cord.
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Now, you note a couple of things.
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The CSF space with intradural extramedullary lesions,
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shows widening at the margins of the lesion.
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So we look for CSF space widening on our T2-weighted scan
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where the CSF is bright.
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With intradural intramedullary lesion,
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you see that the CSF space narrows at the site
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of the primary lesion both above and below
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the lesion or from side to side.
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This is sometimes difficult to distinguish
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from extradural disease, which also causes narrowing.
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But you see that that narrowing is more
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eccentric when you have a lesion that
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is in the extradural space.
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So these features allow us to separate the
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lesions of the spine into separate
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differential diagnoses because intramedullary
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lesions are different in their histology from
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extramedullary lesions and extradural lesions.
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With respect to the intradural intramedullary lesions,
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we're talking about spinal cord lesions.
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And it's important to recognize that the
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spinal cord is separated into the cervical
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region and the thoracic region.
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But by and large, the end of the spinal cord, what we call the
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conus medullaris, ends at approximately the
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L1-level. It may extend to the L1-L2 terminus region here,
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but it's usually above the L2 level.
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The portion of the intramedullary space that persists below
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the L2 level is called the filum terminale.
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However, lesions of the filum,
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although that's the extension of the spinal cord,
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are considered intradural, but extramedullary lesions.
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The anatomy of the spinal cord is somewhat complex.
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Here we see a nice diagram describing the
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various tracts that course through
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the spinal cord. In this diagram,
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the pinkish ones are the ascending tracts,
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predominantly sensory tracts,
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whereas the descending tracts
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are the motor tracts .
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The largest of these will be demonstrated in just a moment.
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What we also note is that the cord gray matter
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is central in location and this is verified on
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the histologic section that is demonstrated to
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the right, with the central gray matter being yellowish
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and the white matter tracts being the more blue color.
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To simplify things for you,
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we think about the main tracts that are in the
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spinal cord, and those are the motor tracts of
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the anterior corticospinal tract and the
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lateral corticospinal tract, and the anterior
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part of the spinal cord, and the lateral
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part of the spinal cord, clearly.
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And then, we have the lateral spinothalamic tract,
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which is largely pain and temperature sensation,
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and the dorsal columns, which are the vibratory
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and position sentence.
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In this diagram, again, you see the central gray matter.
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To identify these components of the spinal cord,
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I think that the gradient echo scans
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in the cervical spine are the best.
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So here we have the histologic drawing.
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Here we have the diagram of the gray matter.
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And as you can see, within the spinal cord,
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there is that type of structure that
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looks like the gray matter
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outlined on the gradient echo scan
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as the brighter areas centrally.
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And then, we also are able to separate the
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spinal cord into the lateral areas with
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the lateral corticospinal tract
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in the spinothalamic tract,
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the posterior column area in the center,
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paramedian region posteriorly,
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and then the anterior corticospinal tracts, as well.
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The importance of this anatomy is that there
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are different syndromes that are associated
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with cord lesions associated with the various tracts.
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So we think of the Brown-Séquard syndrome,
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which is a hemicord lesion which leads to
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ipsilateral sensory and contralateral pain and temperature,
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sensory deficits, as well as ipsilateral motor paralysis because
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of the anterior corticospinal tract and the
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spinothalamic tracts being involved.
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We have the anterior cord syndrome,
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which is usually associated with cord strokes
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and this can cause bilateral pain and
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temperature involvement because of the lateral
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spinothalamic tracts involved,
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as well as the anterior corticospinal
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tract being involved bilaterally.
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And then, we have the central cord syndrome.
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The central cord syndrome is typically what we
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see with degenerative spondylomyelopathy,
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and this will affect the upper motor extremities
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more than the lower motor extremities because
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of the central nature of it, as well as having some motor effect
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because of the central gray matter being involved.
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