Interactive Transcript
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We've just described various vascular etiologies
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for white matter disease that are
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mediated through hypertension.
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This leads to an additional entity known as
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Posterior Reversible Encephalopathy Syndrome,
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which we refer to as PRES.
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So, PRES is mediated through
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changes in blood pressure.
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While initially, we thought that this was
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secondary to hypertension
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and severe hypertension,
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what we've come to understand is that
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fluctuations in the blood pressure
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that may or may not represent hypertension,
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can lead to PRES.
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So, in other words,
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if a patient who normally runs a blood pressure,
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say, of 90 over 60,
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subsequently has an episode
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in which the blood pressure increases to 130 over 85,
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even though it doesn't meet our standard
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criteria of hypertension,
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that fluctuation in the blood pressure can lead
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to posterior reversible encephalopathy syndrome.
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So, this was initially described in three conditions,
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that fluctuations in the
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blood pressure with hypertension,
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eclampsia and preeclampsia,
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with fluctuations of blood pressure
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after birth or at the time of the birth,
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as well as certain medications.
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The classic medication was Cyclosporine.
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We also see this with Tacrolimus,
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but there are many, many medications now
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associated with posterior reversible
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encephalopathy syndrome, so-called PRES.
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All of these seem to be mediated through
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a dysfunction in vasoregulation
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as the blood pressure change exceeds the ability
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to vasoregulate and you get vasogenic
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edema in the posterior white matter.
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from the blood vessels into the interstitium
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and the vasogenic edema.
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You may see mild mass effect.
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Now, the curious thing about posterior reversible
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encephalopathy syndrome,
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is that each of those specific terms
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may not be seen with the entity.
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In other words, we see sometimes PRES
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that is not necessarily posterior,
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but involves the anterior white matter.
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We also see in 10% of cases
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that the patients have infarctions
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associated with the PRES,
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and therefore, it is not reversible.
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90% of the time, it's reversible.
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10% of the time it's irreversible,
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and you have actual infarctions.
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And the E for encephalopathy
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sometimes is relatively minor.
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So, these are different examples
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of patients who have PRES.
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Here is a typical feature in which it's a
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relatively symmetric process,
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which extends to the deep white matter
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in the subcortical region
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and is involving the posterior aspect of the
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white matter in the parietal occipital lobes.
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Contrast that with this patient,
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who has predominantly anterior involvement of
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the frontal lobes.
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Although you do see that
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there is some involvement of the parietal lobes.
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But by and large,
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PRES is relatively symmetric from right to left.
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10% of the cases will show contrast enhancement.
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90% do not show contrast enhancement.
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And as I said,
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only 10% will show cytotoxic edema.
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an ADC map which is showing bright signal
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intensity. PRES, therefore,
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no evidence of infarction. It's vasogenic edema,
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not cytotoxic edema.
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Those patients who have contrast enhancement,
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those patients who have cytotoxic edema,
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and sort of the 10% rule of PRES is the 10%
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are hemorrhagic. Those patients do worse.
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So if you have contrast enhancement,
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if you have cytotoxic edema,
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and if you have hemorrhage,
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the prognosis is worse.
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For more lasting clinical symptoms, however,
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the typical feature of PRES
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is that it is reversible.
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So it does have resolution over the
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course of weeks to a month.
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Rarely,
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you will have involvement of the gray matter,
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which can occur in PRES.
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And you may see mass effect associated
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with PRES as well.
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Women are affected more commonly than men,
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but that is mediated through the cases in which
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you have eclampsia and preeclampsia.
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The etiologies of PRES have
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been widely discussed.
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You can see this in patients who are taking
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cocaine and have wide fluctuations in the blood
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pressure secondary to recreational drug use,
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such as cocaine.
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We also see it in patients who are on dialysis.
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On dialysis, you may see,
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because of the fluid changes,
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wide fluctuations in the blood pressure,
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which may also be seen with PRES.
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You may see this with hepatic insufficiency
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or hepato-renal syndrome.
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You may see this with hemolytic uremia syndrome.
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You may see this with lupus.
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so there are many different causes of PRES
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on the infectious etiologies.
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We see it sometimes in patients who have sepsis,
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and that's usually mediated through vascular
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endothelial injury associated with the sepsis.
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So the list of causes of PRES
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is quite widespread.
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Among the medications I mentioned were
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cyclosporin as well as tacrolimus or FK 509.
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However, almost,
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there are very many chemotherapy agents,
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Ara-C (ARa-C),
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that have been associated with PRES.
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This is what you want to see.
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What you want to see is a patient who has PRES
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that resolves completely. And again,
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this occurs in about 90% of patients.
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If you withdraw the medication,
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if you monitor the blood pressure and
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control the blood pressure swings,
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if you treat the underlying disease,
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such as sepsis, you will see complete reversal.
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Of the disease.
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And that is shown on the MRI scan.
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Remember that the MRI scans tend to be
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delayed versus the clinical response.
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So when they withdraw the medications,
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when they treat the blood pressure,
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when they treat the infection,
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that's leading to the sepsis,
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the patients will respond clinically,
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and the MRI scan might still show the signal
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intensity abnormality in the
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posterior white matter.
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So the MRI is delayed in response compared
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to the clinical response.
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