Interactive Transcript
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This was a patient who had AIDS and was
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initially diagnosed with progressive
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multifocal leukoencephalopathy.
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The initial scan is from August 19, 2013.
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As we look at the FLAIR scan,
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we can see that there is abnormal signal
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intensity in the splenium of the corpus callosum,
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which crosses from right to left.
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We note the involvement of the subcortical U fibers.
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So on this FLAIR scan,
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you can see the involvement going all
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the way out to the periphery,
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which is typical of U fiber involvement with PML.
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Now, there are additional smaller lesions,
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such as this one seen in the subcortical
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subinsular white matter and external
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capsule region on the right side,
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as well as more peripherally
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in the parietal lobe.
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The T2-weighted scan also shows similar
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findings and you note that the lesion does not
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show contrast enhancement on the postgad
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T1-weighted scan here below the FLAIR scan,
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and there is no restriction of
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diffusion on the ADC map.
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The next scan that the patient
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had was from October.
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I'm just going to pull down the
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postgadolinium and FLAIR scans.
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On this October scan,
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you can see that, if anything,
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things have progressed.
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The lesion is larger.
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It remains
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extending to the subcortical U fibers,
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out to the periphery,
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in fact, bilaterally,
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and now is extending even to the optic
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radiations of the temporal lobe.
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The splenium of the corpus callosum actually looks
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a little bit wider and there is
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a little bit of mass effect.
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On postgadolinium-enhanced imaging,
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you can see that there is just faint
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areas of contrast enhancement.
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Here is a demonstration of minimal contrast
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enhancement within the demyelinating process.
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However,
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it can be seen on other such images
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further inferiorly in the periatrial
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region on the right side.
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So, this is a patient whose
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disease is progressive.
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Let's continue to watch this patient over time.
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The patient next gets a scan on December 13, 2013.
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Oh, my goodness.
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This is enlarging into the frontal
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lobe.
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It's extending via the white matter
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tracts into the brain stem.
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The left side is much more
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involved than previously.
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What's going on?
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Let's see what happened on
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the post-contrast scan.
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Oh, my goodness.
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You have avid contrast enhancement.
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The patient's obviously not cooperating,
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and all of a sudden,
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your PML is showing dramatic contrast enhancement.
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What happened?
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Well, what happened between the August study
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and the December study
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was that the patient had
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initiated the HAART,
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the antiretroviral therapy.
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And for whatever reason,
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the patient's PML has dramatically gotten worse,
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rather than what one would have expected
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with it getting better.
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This is the entity known as IRIS,
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Immune Reconstitution Inflammatory Syndrome.
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It is effectively
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PML on steroids, only not really.
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This is PML with marked inflammation,
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which is aggravated by the institution
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of the HAART therapy,
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which leads to jazzing up of the immune response
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such that it overreacts to the PML.
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And in point effect,
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you get abnormal enhancement, mass effect,
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growth in the lesion.
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What can you do?
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Well, at this point,
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the best alternative is to stop the HAART therapy
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and try other medications to relieve
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the patient's AIDS, which was, in fact,
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what was done.
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And we have a follow-up examination,
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somewhat more remote,
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but showing you the residual of what happened.
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So here we have a study from March 5, 2017,
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and you see the remainder of what was the IRIS,
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that is, atrophy,
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enlargement of the ventricles,
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gliosis in the white matter,
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sulcal enlargement showing the volume loss,
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but no mass effect,
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decreased volume of disease,
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and in point of fact,
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absence of contrast enhancement.
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So, the patient actually responded well to the
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withdrawal of the HAART therapy,
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leading to
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still residual disease,
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as far as the sequela of IRIS,
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Immune Reconstitution Inflammatory Syndrome
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in a patient who has PML
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with HAART institution
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or other medications that jazz up and
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reenergizes, if you will,
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the inflammatory system,
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the immune system in the body,
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but it leads to overreaction and more
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disease than the original PML.
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