Interactive Transcript
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So case number two is an 86-year-old
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with memory loss.
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They had an MRI of the brain in 2019,
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which we're looking at here.
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Again, I like to start with the DWI.
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You see the DWI's negatives or no acute infarcts.
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When we look here at the GRE sequence,
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the only thing I see here
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is there's some very faint GRE
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susceptibility artifact here in the left frontal lobe.
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This happens to be if we look
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at the post-contrast image,
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that is right around a large developmental
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venous anomaly.
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So we see that typical Caput Medusae-type appearance
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of a developmental venous anomaly.
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You know, typically,
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DVAs are incidental findings,
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unless they're associated with a cavernous angioma,
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because the cavernous angiomas can bleed.
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In this particular case, though,
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it's slightly unusual because the
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DVA is associated with a small,
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little area of encephalomalacia that you can see here.
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You typically don't see that with a DVA,
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but here's a little brain tissue loss here.
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And again,
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we have a little susceptibility artifact there.
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That's really the only thing that enhances
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on the post-contrast series.
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If you look here in the coronal plane,
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this is, again, that large DVA.
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That's what that looks like.
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Let's look at the T2-weighted sequence,
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and I'll pull back up the FLAIR here.
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So on the FLAIR,
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we see all this area of patchy FLAIR hyperintensity
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throughout the brain.
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This patient has moderately severe,
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that tells us this patient has moderately severe
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baseline microvascular ischemic disease.
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They also have old lacuna.
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Here's an old lacuna in the right hemipons.
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So, there's fairly significant
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microvascular ischemic change here.
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If we look at the T2-weighted sequence,
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which is a sequence I like to use to assess for atrophy,
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we see there's mild to moderate cerebral atrophy with a
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right mesial temporal and also a
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biparietal predilection here.
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The only other thing that we...
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just little incidental finding that we have,
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there's a little bony exostosis.
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I'll show you that.
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And the only reason I mentioned this is because it can
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be confused if it's calcified potentially
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for a little meningioma.
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Here it is here along the left frontal convexity,
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and here it is on the post-contrast sequences.
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But we see that it's actually high in signal on T1,
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so it's more likely to be just a bony exostosis
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rather than a tiny meningioma.
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There's no definite convincing enhancement on
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the surface of this.
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So, let's move now.
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In 2009,
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the patient then went on to have an FDG brain PET CT.
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Here's the FDG brain PET CT.
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I'm going to invert here.
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And this demonstrated statistically significant cortical
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hypometabolism in the right temporal lobe.
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Here.
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And also in the right posterior cingulate gyrus,
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we also had, statistically significant,
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hypometabolism in the left frontal lobe,
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but nothing in the right frontal lobe,
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and it's really only in the medial
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aspect of the left frontal lobe.
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So, interestingly,
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this is where we had that big DVA
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with the little area of encephalomalacia.
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But it's not really looking like an FDG type pattern.
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You know,
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the right frontal lobe is completely normal.
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This really appears to be related to the inflammatory
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response around that DVA,
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which is, again, quite unusual.
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But that happens to be what we see in this case.
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And then,
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if we look at the patient then came back for
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an MRI in 2016.
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So, I'll pull up some images here.
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So, the images on the right here are 2016.
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I'll pull up comparison images from
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2009 on the left-hand side.
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Okay.
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And what we see here is dramatic interval progression
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in the amount of cerebral atrophy
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with a temporal predilection.
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So now, we have moderately severe to severe atrophy
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in the bilateral temporal lobes.
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Again, right more than left.
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So it's kind of moderately severe in the left,
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moderately severe to severe in the right temporal lobe,
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and moderate to moderately severe
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in the bilateral parietal lobes.
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That represents a significant progression
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from the 2009 study.
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Microvascular ischemic disease
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has also significantly progressed.
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It's now relatively severe in degree.
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We also have multiple new...
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Well, they're not new infarcts,
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but they are new since the prior exam,
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so they weren't present on the prior.
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If we look here in the left thalamus,
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we also have one here in the right caudate nucleus.
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We have new ones here,
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new one here in the left pons.
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The one in the right hemipons was present on the prior,
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but the microvascular ischemic change in old infarcts
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has definitely progressed since the prior study.
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So case two, again, was the 86-year-old
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with memory loss.
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Here's their MRI in 2009,
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where we have some atrophy with a right temporal
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predilection, mild to moderate in degree.
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The patient also then went on to have
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an FDG brain PET CT in 2009.
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Again,
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I run all of these PETs through the
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neuroanalysis software,
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which indicated that there was statistically significant
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hypometabolism in the right temporal lobe.
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You actually see hypometabolism in
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the bilateral temporal lobes,
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but it was statistically significant on the right side.
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By the way, this is the FDG PET CT,
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and this is the PET MR fusion.
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You can clearly see some hypometabolism
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here in those temporal lobes.
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There was also hypometabolism again in the right
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posterior cingulate gyrus,
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and then in the left frontal lobe,
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from that DVA.
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The patient then came back in 2016.
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And now, we have pretty severe atrophy in the bilateral
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temporal lobes, right greater than left,
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and quantitative volumetric imaging
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was also done in 2016.
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Here's NeuroQuant and icobrain.
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And we have statistically significant reduction in
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the volume of the hippocampal occupancy score
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and the hippocampus,
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as well as statistically significant enlargement
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of the inferior lateral ventricles.
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And those same things are also demonstrated
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here on the icobrain report.
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This is, again, a closer look at the NeuroQuant.
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Here's the plot graph here showing
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statistical significance.
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We're down at 1% for the hippocampus and
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99% elevated for that inferior
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lateral ventricular volume.
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And you might be wondering what the
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hippocampal occupancy score is.
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This is just an estimate of the
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degree of hippocampal atrophy.
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So, it's just the left hippocampal volume divided by
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the left hippocampal volume,
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plus inferior lateral ventricular volume.
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Plus, on the right side,
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those same value,
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the same thing on the right side,
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then they're average and normalized.
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So, the lower hoc scores are highly associated with
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progression from mild cognitive impairment
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to Alzheimer's disease.
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So the bottom line, really,
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the only thing you need to remember is that the lower
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hoc is the more at risk the patient is for developing
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Alzheimer's disease.
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And again, that hoc is...
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we saw that on the quantitative volumetric report.
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This is just the triage brain report in 2016,
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and we're looking for overall patterns.
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In the overall pattern here in the temporal lobe,
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we see a lot of red boxes here in the temporal lobe.
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This was the icobrain report from this patient.
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By 2016, really,
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there was statistical significance in every lobe
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of the brain, including in the hippocampi,
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all less than 1%.
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There's a second page of the icobrain report.
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Again, the whole brain volume is down now at less than 1%.
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The other summary images that we had already reviewed,
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the large DVA,
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the little area of encephalomalacia here,
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minor hemosiderin staining associated with that.
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Here's that DVA again.
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And here's some of the hypometabolism that
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we saw in the left frontal lobe.
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The patient then went on to have an amyloid PET in 2016,
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and that was positive.
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Here's the grayscale,
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diffuse binding of the amyloid tracer to the cortex.
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Same thing we see here on the color fusion.
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