Interactive Transcript
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We're about to proceed from the neoplastic
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category and demyelination category,
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to the congenital category
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in looking at lesions of the intradural
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intramedullary spinal cord. Far and away,
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the most common is going to be syringohydromyelia
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associated with a Chiari I malformation.
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As we look at this T1, T2, and STIR image.
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what we see is the cerebellar tonsils are
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descended through the foramen magnum.
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We can measure this by drawing a line across the
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foramen magnum and then the depth of the
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cerebellar tonsils,
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and this measures 9 mm down here in yellow.
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9 mm is above the threshold, we usually set at
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5 mm below the level of the foramen magnum
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for cerebellar tonsillar descent.
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Over the course of the past several years,
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we've discovered a number of cases of.
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intracranial hypotension, secondary
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to CSF leakage in the spine,
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which has led to acquired cerebellar tonsillar
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descent through the foramen magnum.
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So this is now a differential diagnosis,
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not just a willy-nilly diagnosis of Chiari I malformation.
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Now we have to look for other manifestations,
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potentially of intracranial hypotension.
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Whenever you have cerebellar tonsils extending
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through the foramen magnum,
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you have the potential for alteration
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of the CSF flow mechanics.
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And that can lead to the presence of syringohydromyelia .
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The purists would say that hydromyelia
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is dilatation of the central canal
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of the spinal cord, whereas a syrinx is a cavity
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or fluid collection eccentric from the
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central canal of the spinal cord.
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Because in many instances, we can't tell whether
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it's actually eccentric or centrally
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located within the spinal cord.
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We will combine the two terms and use
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syringohydromyelia. Classically with Chiari I
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malformations, tonsillar herniation
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through the foramen magnum,
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it is classically a hydromyelic cavity.
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And the etiology for this appears to be that
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with the obstruction of normal CSF flow, the
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pressure builds in the spine and is transmitted
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along the perivascular spaces of the spinal cord
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into the central canal where it decompresses
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in the spinal cord.
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So this is the explanation for why one gets
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hydromyelia associated with a Chiari one malformation.
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The treatment for the Chiari I malformation
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is a suboccipital decompression procedure,
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often taking the posterior arch of C1 because
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this also contributes to the narrowing.
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And then there is a duraplasty procedure to
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expand the CSF cavity, so that way the tonsils.
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freely move in the CSF space and there is good pulsation.
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This patient has superimposed degenerative disc disease.
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You notice a herniation at C4-5
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and again at C6-7, and also has one of the characteristic
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features of syringohydromyelia.
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and that is that there appear to be webs or
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multiple cavities to this collection that you're
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seeing on the T1 and T2-weighted scans.
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So,
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Chiari I malformation associated
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with hydromyelia or syringohydromyelia.
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Remember that we use the term Chiari I
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malformation in those cases that do not have
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congenital myelomeningoceles. For that,
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we will use the term Arnold Chiari malformation.
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