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Parkinsonian Syndromes: MSA-P

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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.

Report

Description

Faculty

Stephen J Pomeranz, MD

Chief Medical Officer, ProScan Imaging. Founder, MRI Online

ProScan Imaging

Tags

Neuroradiology

Metabolic

MRI

Brain

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