Interactive Transcript
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This is a 52-year-old woman with intractable
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Parkinson's disease that did not respond to
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typical dopaminergic medications like Sinemet.
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Let's scroll her in the axial projection.
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She's got a known Parkinson syndrome.
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Going to make it a little bigger for you
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so you can see the midbrain.
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And let's see if she's got a preserved
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compacta stripe.
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And she does.
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You see the red nucleus separate from the iron
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stores in the rest of the substantia nigra
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with a preserved compacta stripe in between
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with the two not bleeding together
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as they would in somebody with
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a severe Parkinsonian syndrome.
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So what are we going to do?
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How are we going to look at this image?
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How are we going to attack this case?
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Well, first, let's go up and look at the cortex.
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Let's see what kind of atrophy she has.
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Not much.
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In fact, very little atrophy.
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And the reason I want to go upstairs and look there
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is because I'm going down my checklist
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of Parkinson-like syndromes,
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assuming that there's no medication
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that's causing this,
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because medication can cause
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a Parkinson-like syndrome too.
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So what am I looking for up high?
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Atrophy?
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Especially asymmetric atrophy as might occur in
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corticobasal degeneration doesn't have it.
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So, now, let's go down low.
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Let's look at the temporal horns.
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They're a little bit dilated,
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but the parahippocampi look pretty juicy.
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Let's pull down a coronal
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and see just how juicy they do look.
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They're a little bit atrophic.
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The choroidal fissures are a little big.
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The horns, the temporal horns are a little big.
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So I would include,
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in my differential diagnosis here,
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Lewy body dementia.
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However, I would not include Alzheimer's disease,
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even though the entorhinal cortex
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is somewhat atrophic,
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because this patient is presenting with a severe
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intractable Parkinson's-like syndrome.
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So it doesn't fit historically.
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In addition,
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I don't really have a lot of parietal atrophy,
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which you see in patients with
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Alzheimer's disease.
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Most of the atrophy that I'm seeing that is
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cortically based is sylvian and frontal.
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So that doesn't fit very well.
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Another condition associated with a Parkinson-like
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movement disorder is frontotemporal dementia.
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Now, that one would remain in the
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differential diagnosis,
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except that these patients have a lot of
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behavioral disturbance, dysexecutive function.
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In other words,
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they do things that are ill-mannered.
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They lose their inhibition.
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They do have frontal atrophy,
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which this patient has.
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They do have temporal atrophy,
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which this patient has.
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And they do have a Parkinsonian-like syndrome.
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So that remains of the differential diagnosis,
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but the history goes against it.
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In other words, the patient doesn't have
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this detached, dysexecutive, ill-mannered behavior.
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So clinically, this helps you a lot.
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Another aspect of this case that goes
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against Lewy Body Dementia,
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which is strongly associated with
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a Parkinson-like presentation,
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is the absence of visual hallucinations.
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Now, another disorder that you would consider is
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progressive supranuclear palsy.
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So I'm listing,
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I'm going right down the list
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of Parkinson's plus syndromes.
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So, let's talk about PSP.
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I'm going to blow up the brainstem for a minute.
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The cerebellum is not very atrophic.
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If we look at the brainstem in the midline,
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it looks like the colliculus is atrophic,
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but it's not.
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You're just in the sulcus.
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If you go off to the side, it's nice and juicy.
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If you go off to the other side,
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it's nice and juicy.
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And the superior colliculus
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is as big as the inferior colliculus.
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Therefore, you do not have the diagnosis of PSP,
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Steele Richardson-Olszewski syndrome
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or progressive supranuclear palsy.
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So, now, I'm down on my luck.
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I'm down on my list.
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I'm down to MSAP,
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multi-system atrophy Parkinson's type.
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There are three basic types of MSA.
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There's MSAA,
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autonomic dysfunction.
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Patients have trouble standing in one place.
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They get hypotensive.
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Also known as the shy-drager variant.
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You have MSAC
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where there is severe pontocerebellar atrophy
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associated with the hot cross bun sign,
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and then you have individuals that have MSAP,
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where they have a Parkinson's-like syndrome.
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The atrophy is very nonspecific,
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although it can involve the pyramidal and / or motor system,
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it can involve the frontotemporal region.
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In fact, it can be just about anywhere.
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So your differential diagnosis would come down to,
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in this case,
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frontolobar dementia or frontal lobar disease,
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also known as Pick's disease, and MSAP,
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with Lewy Body Dementia being a less likely
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consideration due to the history.
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And unfortunately, in this case,
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the patient succumbed and was found to have MSAP,
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Multi-system atrophy Parkinson's type.
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