Interactive Transcript
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This is 74 year old man who s been carried for
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some time seven years with a diagnosis of classic
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PD or Parkinson's disease. However,
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his cinemat or DOPA response was variable to nil.
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Now, a key part of this patient's history was
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dementia at presentation on MRI.
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And his dementia had been present for at least 5 years.
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So, five out of the seven years.
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So the fact that dementia was a prominent
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presentation early on,
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might have been a tip off
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to the pathologic diagnosis in this case,
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which we do have.
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Let's look at the axial echoplanar image,
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an axial PD and an axial T2.
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What might strike you is the thickness
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of the substantia niagara,
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the preservation of pigment in the red nucleus,
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and the fact that you can see the compact zone
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separating the two.
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So they haven't completely bled together.
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This is apparent on the PD,
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the T2, less valuable because it's
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not as sensitive to iron.
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And I'm going to scroll up and down a little bit.
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As you can see, there's iron accumulation in the putamen,
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less so in the globus pallidus,
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maybe the GPE, the outer aspect of the globus
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has a little bit of brain iron in it.
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Let's go up and then let's go down a little bit,
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back to the level of the midbrain.
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We'll go a little bit below towards the midbrain
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pontine junction, just so you get a feel for it.
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And once again,
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in somebody with really severe end stage
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Parkinson's disease, quote unquote,
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which this patient was alleged to have,
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the preservation of the compactor
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stripe goes against classic PD.
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Then I'm going to pull down the sagittal,
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remembering that this patient has dementia,
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and I'm going to scroll from side to side.
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Let's go off to one of the temporal lobes.
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Actually,
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let me get something that's a little thicker here.
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Let's go off to one side and look at the
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massive atrophy of the temporal lobe.
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It's way disproportionate than you would expect
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for somebody who has seven years
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of Parkinson's disease.
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Let's go to the other side where the temporal lobe
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is also severely atrophic.
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So early dementia,
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disproportionate atrophy in the temporal,
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hippocampal and parahippocampal regions,
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and the preservation of the compacta zone
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raise the possibility of a very closely
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related Parkinsonian disorder,
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namely LBD or Lewy Body Disease or dementia,
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which includes dementia with Lewy bodies.
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Dementia with Lewy bodies is also
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seen in Parkinson's Disease,
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but the dementia is a late component or a
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later component of Parkinson's disease.
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This is one of the more common forms of dementia.
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It accounts for 15% of all cases at autopsy,
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the most common being, ALZ or Alzheimer's disease,
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but tied or maybe slightly more frequent is
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frontalobar dementia.
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So it goes ALZ, then DLB,
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and frontal lobar dementia,
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in the spectrum of dementia,
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the risk of progression to dementia and
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Parkinson's disease increases with age.
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So if you get Parkinson's disease at age 70,
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you're more like likely to have dementia
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in the earlier spectrum of the disease.
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Whereas if you get Parkinson's
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disease when you're 30 or 40,
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the dementia component doesn't appear until very,
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very late.
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The dementia component has been shown to affect
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70% of all PD patients over an eight year
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prospective longitudinal study,
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and it's six times more frequent than
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in healthy control subjects.
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So it is related to the disorder,
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not some overlap or additive disorder that causes
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the dementia in PD or classic Parkinson's disease.
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Now, DLB,
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Lewy Body Dementia or LBD
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and Parkinson's disease
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are differentiated from other dementia subtypes
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by the presence of Lewy body pathology.
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Both groups have alphas and
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nuclear fibrillary aggregates,
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which form neuronal inclusion bodies that are
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known as Lewy bodies and Lewy neurites.
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So lewy bodies are not unique to Lewy Body Dementia.
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Lewy bodies occur in PD as well.
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And that's a potential exam or board question for
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medical students and residents and fellows.
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Let's move on.
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This patient,
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a Parkinsonian like syndrome,
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Lewy Body Dementia,
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rather than classic Parkinson's disease,
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sadly confirmed at post.
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