Interactive Transcript
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Dr. Laser,
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this is a 59-year-old woman with severe progressive
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mental status change that they said began one year ago,
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worsen over the last three months.
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The timing, you know, is in question
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because, of course, patients don't often report
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that they have cognitive decline.
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People from the outside recognize it.
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So, probably been going on longer than that.
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But we've got an axial T2 with some
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rather profound frontal atrophy.
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Not so much parietal involvement this time.
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The ventricles aren't that big.
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Here's a coronal FLAIR demonstrating some
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periventricular disease and some white matter
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scattered gliosis throughout the brain,
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but not a prominent finding in this case.
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What is a prominent finding is the profound frontal
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atrophy that is worse on the left and right with
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extensive prominence of the Sylvian fissures.
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And then as we come forward,
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all the way into the olfactory area,
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that's atrophic too,
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although not quite as severely affected.
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But look at this pattern of atrophy,
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which you would call what?
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It has the...
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The gyri have actually shrunken down and atrophied
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in terms of like a sharp knife.
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So it's called the knife blade.
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Knife blade atrophy.
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Atrophy.
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All right.
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And then we go over to the sagittal.
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We go over into Broca's area,
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and the normal letter M for Broca's area is distorted.
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And the typical Broca area, Broadmann 44 and 45,
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affected as well in this ascending portion, or ramus,
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of the insula, is affected anteriorly.
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And then there is extensive temporal atrophy,
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although the tip is spared.
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And we're going to look at the entorhinal cortex,
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the meat of the hippocampus,
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and that's not much affected either.
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Look how good the choroidal fissures and temporal
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horns look relative to everything else.
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Granted they're not perfect,
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but they're pretty good compared to the severity of
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atrophy you have elsewhere.
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So all of those findings,
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hippocampal sparing, knife blade atrophy,
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frontal predilection, frontotemporal involvement,
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a little bit of olfactory involvement.
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What does that suggest to you as a dementia?
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Oh, with her symptoms,
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frontotemporal,
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low bar degeneration.
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Yeah.
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Formerly known as the artist pick's disease.
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So, let's talk a little bit about Pick's disease.
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It may involve the basal ganglia.
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In this case, the basal ganglia,
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when we scroll through them, looks pretty good, actually.
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And pretty juicy-looking
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globus pallidus and putamen.
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We go over to the caudate nuclei.
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They look pretty good, too,
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so they're not really all that atrophic.
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And so, basal ganglion involvement here scanned.
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And then, what defines this disease is the presence
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of specific inclusions containing tau,
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such as TDP 43 or ubiquitin,
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which allows biochemical classification of this disease.
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It's noted for being an asymmetric disease,
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and even though there's a fair amount of symmetry
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in the temple region, as discussed previously,
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there's quite a bit of asymmetry in the frontal region,
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left greater than right.
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Now, when the left is more affected,
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what is the primary presentation?
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Or what can be one of the major symptoms?
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Typically, it's aphasia.
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Semantic aphasia.
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A semantic aphasia.
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The meaning of words is lost.
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And we've already seen that the Broca area is involved too,
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so that's problematic.
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When it's on the right side,
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predominantly, they present quite a bit later.
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They may complain of difficulty with facial recognition.
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So this is an individual with Pick's disease,
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demonstrating all of the cardinal findings.
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In the next vignette, companion vignette,
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we're going to talk about the subtypes of Pick's disease
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and a little bit more about their presentation,
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which includes something called the disexecutive syndrome.
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You know,
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when you eat with your feet at the dinner table?
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Yeah. Loss of filter. Yeah.
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But we both know what that's about.
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Yeah.
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Pomeranz and Laser out.
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