Interactive Transcript
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This was a two-year-old who presented with failure
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to thrive and not meeting milestones.
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On the T1-weighted scan,
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we look at the brain and we assess it as showing
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a normal size, so no evidence of macrocephaly.
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On the FLAIR scan,
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we see a white matter disease,
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which is predominantly central in its
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location and is symmetrical.
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We also note that the patient has an arachnoid cyst
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which is causing remodeling of the
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greater wing of the sphenoid.
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But let's dispense with that because that's irrelevant
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to the case of a dysmyelinating disorder.
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This dysmyelinating disorder affects
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both the genu and the splenium of the corpus callosum.
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But what one can see is that it spares
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the subcortical U fibers.
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So we see the involvement centrally,
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but you're not seeing involvement going
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out to the subcortical U fibers,
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which would be typical of other dysmyelinating
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disorders other than this case,
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which is metachromatic leukodystrophy.
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Since metachromatic leukodystrophy is the
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most common of the dysmyelinating disorders,
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we might want to look for the so-called tigroid
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stripes that are characteristic
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of this dysmyelinating disorder.
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For the tigroid stripes, we look at the
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periphery of the ventricles,
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and we see the little dots of the
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somewhat spared white matter.
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Let me demonstrate this.
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So in this case,
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you see these little dots where
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there is not homogeneous dysmyelination,
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but there appear to be little areas of darker signal
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amidst the FLAIR abnormality of the dysmyelination.
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In point of fact,
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if we look at this particular image,
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we can identify the characteristic feature
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of those tigroid stripes.
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So, here we see dark signal intensity
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going out to the periphery.
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Here's another area of these stripes of white matter
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that is not involved with the dysmyelinating disorder.
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At the same time that you can see some of the dots of
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white matter fibers that have been cut in cross
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section as they are coursing superiorly in the brain.
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So, this characteristic of sparing of these
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subcortical U fibers and the tigroid stripes
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leads us to the diagnosis of metachromatic leukodystrophy.
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We can also verify this when one looks
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at the MR spectroscopy
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that was performed at the same time
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on this patient.
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And what one sees on the MR Spectroscopy
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is depression of the NAA,
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not elevation of the NAA.
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So, in the differential diagnosis of metachromatic
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leukodystrophy is Canavan's disease,
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where we would expect to see the big NAA spike
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and the lower choline and creatinine spikes.
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In this case, we see that the NAA is,
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if anything, somewhat lower,
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which confirms the diagnosis of metachromatic
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leukodystrophy by virtue of absence of NAA elevation.
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We also do not see the macrocephaly,
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which is typically of
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Canavan's disease and Alexander's disease.
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