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Bilateral Corpus Striatum Caudoputamen Hyperintensity Differential Diagnosis

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Let's take a look at a 64 year old woman who

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presents with cognitive issues,

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ataxia and dystonia.

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First of all, what is dystonia?

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Dystonia is a movement disorder which your muscles

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contract involuntarily,

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causing repetitive or twisting movements.

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It's important to understand the distinction

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between these disorders, because in this case,

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we've got an axial FLAIR on the left,

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a T2 fast spin echo in the middle,

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and a T1 on the right.

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There is putaminal loss of volume,

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but there's also bilateral

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putaminal hyperintensity.

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And the caudate is also hyperintense,

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but it's not very atrophic.

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In addition, the patient doesn't have Chorea.

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They do have cognitive dysfunction.

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So whenever you see a caudoputaminal disorder with

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cognitive dysfunction in a middle aged patient,

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50, 60 years of age,

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you got to think about Huntington's Chorea,

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which can occur, by the way, at any age.

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But the fact that you have a pretty

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robust appearance, in fact,

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a very robust appearance of the caudate,

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both the head and the anterior body goes

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very much against Huntington's Chorea.

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Look at how it indents the ventricles.

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Look at the T1, the gray matter indentation,

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best seen right here.

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So, Huntington's Chorea is out for a few reasons.

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That's one,

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the fact that it's dystonia rather

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than Chorea is a second.

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Now, what are some other considerations

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when you have dystonia?

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This condition can affect any part of the body,

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but it's usually segmental in one part of

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the body, or it can be generalized.

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The muscle spasms range from mild to severe,

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but must be differentiated from another condition

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that you'd have to consider here,

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and that is corticobasal degeneration.

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It's called corticobasal degeneration

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because it involves the cortex and the basal ganglia.

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Let's look up at the cortex.

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There is some atrophy.

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It's mild, it's generalized, it's diffuse.

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And there is involvement of the corpus striatum,

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the caudate nucleus in the putamen,

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especially atrophy of the putamen.

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But what differentiates CBD (corticobasal

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degeneration) from this disorder, this dystonia?

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And the answer is, in CBD,

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there is usually one arm or one

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extremity that's affected,

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and then it spreads to other extremities.

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And it's not a dystonic contraction.

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It's more of an apraxia,

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where the patient has difficulty doing purposeful tasks.

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They have the muscle strength to do it,

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they just simply can't do it.

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So, the differentiation between this condition and CBD

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is often going to be made on clinical grounds.

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What other disorders would you consider

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with dystonia and disappearance?

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Well, one of them is Leigh's disease,

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an abnormality of pyruvate carboxylase,

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an enzyme,

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present exactly like this,

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except the patient is 64 years of age.

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It's very unusual for dystonic presentation

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of Leigh's disease in an adult like this.

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Usually in young juveniles and early adulthood.

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So because of the age, that one is out,

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what about another condition that can affect both putamena?

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Well, one of them, a toxic condition,

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is Wernicke's encephalopathy.

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It's closely related to Leigh's disease and some of

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the other disorders because they all have an

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effect on metabolism and ATP and oxygenation.

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Let's talk about bilateral putaminal involvement

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in Wernicke's encephalopathy.

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First, you should have a history

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of alcoholism or some type of toxicity.

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Second, you should have mammillary body atrophy.

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Let's see if we do.

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Let's look in the sagittal projection.

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In fact,

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we've got a juicy mammillary body

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it's of normal size.

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Third, we might have hemorrhage in the mammillary body.

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We don't.

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So Wernicke's encephalopathy,

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which is a toxicity,

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an acquired condition which, by the way,

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is associated with a movement disorder,

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but not dystonia,

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is not going to be the diagnosis here.

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What are some other causes of bilateral

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corpus striatum,

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caudoputaminal hyperintensity?

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Well, there are a number of other toxicities

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exogenous that can do it.

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So you'd want to do a urine and blood screen,

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but there are also a number of endogenous

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toxicities that can do it.

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And what is an endogenous toxicity that could do this?

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And the answer is Wilson's disease.

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Wilson's disease,

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a disorder of copper metabolism.

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And we're going to talk about Wilson's

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disease in the follow-up vignette.

Report

Description

Faculty

Stephen J Pomeranz, MD

Chief Medical Officer, ProScan Imaging. Founder, MRI Online

ProScan Imaging

Tags

Vascular

Syndromes

Non-infectious Inflammatory

Neuroradiology

Metabolic

MRI

Infectious

Idiopathic

Drug related

Brain

Acquired/Developmental

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