Interactive Transcript
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This next case is a 41-year-old
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woman who had double vision.
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While initially one might think about scanning
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the orbits to look for optic neuritis
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in a patient who might have multiple
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sclerosis history.
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For most patients who have double vision,
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we scan the brain first,
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and the orbits may not be separately included.
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This patient shows a number of areas
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of abnormal signal intensity,
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as you can see in the white matter.
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And if we look on the T2-weighted scan,
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the infratentorial fossa and the brain stem look
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pretty good, in that there are no areas of
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demyelination seen on the T2-weighted scan.
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As we shift to the FLAIR scan, however,
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we see lots of white matter lesions that
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are in the periventricular zone.
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I'm going to stop on this case
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on this image to identify the demyelinated
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plaques on the FLAIR scans.
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And again,
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we would comment about the closeness this is
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to the gray matter as a juxtacortical
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or subcortical white matter lesion,
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as well as some deeper white matter lesions.
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And as we scroll these scans,
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you see that some of them actually extend
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to the periphery of the ventricle.
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So a nice example of a large plaque,
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which spans from the ventricle to the subcortical region.
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The other thing I want to emphasize on this
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particular case is the presence of cytotoxic
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edema around some of these plaques.
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So, if we go up into the higher portions of the
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centrum semiovale and we look at the ADC map,
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we do see a small halo of dark signal intensity
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around the area where there is T2 shine
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through in these demyelinating plaques.
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So this is an example of ADC
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positive demyelination.
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And we would suggest that this implies
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that this may be an active plaque.
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If we pull down the postgadolinium-enhanced scan
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and scroll to that same region,
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we can see a small amount of peripheral and
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nodular enhancement along these plaques that
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suggest that indeed they are active.
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We also see inactive plaques.
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For example,
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in the right temporal region,
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we have an area of demyelination that
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is seen well on the FLAIR scan,
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but no evidence of enhancement.
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And in this one,
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along the periventricular region near the temporal
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horn of the lateral ventricle,
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no area of contrast enhancement.
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Looking at the region around the
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optic canal,
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we get lucky here because, indeed,
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on the postgadolinium-enhanced images,
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one can see the optic nerve coursing to and through
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the optic canal showing contrast enhancement,
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suggesting that the patient
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may have optic neuritis.
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This patient had a prior study that showed a nice
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example of the findings you might see
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on the cervical spine examination.
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So, what we're seeing is on the T2-weighted
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scan to the far left and the STIR
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image to the far right,
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an area of demyelination in the
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upper cervical spinal cord.
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It happens that, in this example,
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one sees that the cord is slightly expanded
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in an anterior-posterior direction.
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You might also suggest that there's likely to be
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another demyelinating plaque lower down
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on the periphery of the spinal cord.
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So let's indeed look at the T2-weighted
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and gradient echo scans.
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So here we have the gradient echo scan,
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and here we have the fast spin echo T2-weighted scan.
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They're both T2-weighted but one sees the
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area of demyelination in the right side
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of the spinal cord.
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In this case,
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I'd say maybe a little bit better on the
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fast spin echo scan than on the gradient echo scan,
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and that is in the upper cervical
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spine at the C2 level.
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As we scroll the images down lower,
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we can see that both of these sequences are
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showing the demyelination in the right
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side of the spinal cord quite nicely.
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And as we get to the periphery of the spinal
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cord lower down at that C4-5 level,
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we can also see the area of demyelination along
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the periphery of the right
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side of the spinal cord.
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So here, we see that on the fast spin echo,
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the edge of the spinal cord is bright
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in signal intensity.
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This corresponds to that same location
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on the sagittal STIR,
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and the same thing is also
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true on the gradient echo scan.
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Some multiple areas of demyelination
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in the spinal cord
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on the
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cervical spine examination.
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By virtue of this patient having periventricular
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white matter lesions,
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subcortical white matter lesions,
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as well as spinal cord lesions,
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Some of which are showing contrast enhancement.
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We have fulfilled the McDonald criteria for
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dissemination in time and space,
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and therefore,
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meet the criteria for making a diagnosis
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of multiple sclerosis.
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