Interactive Transcript
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The next entity to describe in this great parade
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of demyelinating disorders is progressive
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multifocal leukoencephalopathy, or PML.
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You can see that these have all long names,
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and that's why we tend to go with things
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like ADEM and MS and MDEM and PML.
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A lot of short acronyms or the abbreviations.
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PML is an entity that is associated
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with the Papovavirus,
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the JC virus, that destroys oligodendrocytes,
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and hence leads to the white matter disease.
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It's typically found in immunocompromised hosts.
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And while initially this was a boon in the
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AIDS epidemic era, where we saw many,
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many cases of PML,
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it has subsequently transferred
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to those patients who are undergoing
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immunosuppressive therapies,
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such as organ transplants or chemotherapy for
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cancer or lymphoma.
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This is an entity that has usually
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little to no enhancement,
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but will favor the subcortical U fibers on MRI scan.
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It does have a posterior predilection,
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so we see it more commonly in the occipital lobes,
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as well as the parietal lobes,
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and you may also see it in the cerebellum
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and brain stem.
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This is a nice example of PML,
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a typical stereotypical involvement
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of the white matter.
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We notice that we have a confluent
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white matter lesion that is multifocal.
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We're seeing it in the frontal lobe,
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as well as in the cerebellum.
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When we look at its extent,
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as opposed to something like multiple sclerosis,
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it extends to the subcortical
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U fibers in a confluent way.
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This is probably best demonstrated
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here in the cerebellum,
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where you see it going all the way to the
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periphery in sort of a claw-like fashion,
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not staying centrally that one would see
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in other demyelinating disorders.
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On diffusion-weighted scan,
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it is not showing restricted diffusion.
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So less than 10% of cases of PML
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have restricted diffusion or decreased ADC,
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and less than 10%
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have gadolinium enhancement.
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You see here that this lesion is not
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showing gadolinium enhancement.
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Less than 10% are hemorrhagic.
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So, this is our stereotypical view of progressive
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multifocal leukoencephalopathy.
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I would like to draw in a little bit of white matter disease,
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more in the parietal region
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for that posterior predilection,
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but in this case,
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the patient's predominant involvement was
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frontally in the supratentorial compartment,
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but out in the periphery of the cerebellum,
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in the infratentorial compartment.
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