Interactive Transcript
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When we have a child presenting with acute neurologic
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deficit where a stroke is considered, we might
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start out with an MRI study rather than a CT study.
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Again, remember that the CT, CTA, and CT
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perfusion is multiple scans of the same anatomy
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again and again as part of that CT perfusion,
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and therefore, it is a higher radiation
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dose than a simple CT scan without contrast.
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So therefore, in the children who are
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suspected of having a stroke, we might start
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with an MRI scan because of the absence
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of any radiation exposure to that patient.
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This was just such a patient—
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a child who presented with
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aphasia.
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So, children presenting with possible stroke,
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we have a different differential diagnosis,
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obviously, than an adult where we're
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most likely considering atherosclerosis.
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So let's look at this patient.
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Here is the diffusion-weighted scan.
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Again,
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the first thing I'm going to go to is
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the DWI to determine whether there's a stroke.
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Time is brain, so I go to the DWI, and on this DWI,
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pretty clearly, you see that there is a relatively
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large area of infarction within the left middle
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cerebral artery distribution that is affecting not
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only the caudate nucleus and the putamen, probably
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a portion of the globus pallidus, as well as the
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frontal opercular region and perisylvian region.
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You also see that there are other areas
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of left frontal lobe infarction.
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So I've gotten infarction.
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I'm on the phone calling the clinician as I
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continue to look at the additional whole sequences.
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So the next thing to do is we're gonna look
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for our gradient echo or susceptibility-
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weighted scan to see whether there's any
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hemorrhage in this area of infarction.
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And we do not see blood
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products, so that's a good thing.
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So the patient is potentially a candidate for
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a thrombectomy if that is indeed present.
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And next, we would go on to the MRA.
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I just wanna make a comment about the value of FLAIR
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imaging and diffusion-weighted scanning together.
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So what we have
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found in neuroradiology is that a patient
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who has a diffusion deficit on the DWI, where
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the FLAIR scan is still normal, usually means
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that the infarct is less than six hours old.
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However, if we see the abnormality on DWI
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and bright on the FLAIR scan, which you see
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here, it's usually greater than six hours old.
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That's useful because the sooner we get to do
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thrombolysis or thrombectomy, the better the prognosis.
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In some cases, something that we
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would call a "wake-up stroke."
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The patient wakes up from sleep with a neurologic deficit.
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We don't know how old the neurologic deficit is.
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The DWI-FLAIR combination would be able to separate
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it into those that are six hours or younger.
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Versus those that are older than six
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hours on a wake-up stroke, where you don't
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know when the patient was last normal.
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So in this child, we're saying, all right,
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well, this stroke is greater than six hours old.
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It's still possibly one that we would intervene on.
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So we would want to go to the
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MRA in the MR perfusion study.
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Here is the MRA study, and I'm going to get to the tumble
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view, which is my favorite view, where we're seeing.
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The vessel look head over heels.
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And what we see on this head-over-heels view is
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that the M1 segment of the middle cerebral artery
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on this patient is showing areas of narrowing and
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expansion and narrowing and expansion across the M1
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segment compared to the contralateral right side.
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So this is an abnormal segment of
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the blood vessel, and we do not see.
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Thrombosis; what we see is vasculopathy.
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So the differential diagnosis for vasculopathy in a
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teenager, a 12-year-old, 13-year-old, as in this
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case, is relatively wide, is my portion of geography.
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One of the more common etiologies
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would be sickle cell disease.
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Where you may have a vasculopathy on that basis and
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or thrombosis on that basis in a different age group.
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We might also consider IV drug abuse with
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a vasculopathy or vasculitis on that basis.
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Secondary to illicit drug use or cocaine use, for
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example, could cause a vasculitis or vasculopathy.
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There are some other entities,
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collagen vascular diseases such as.
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You know, your sarcoid or lupus or other
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rheumatoid etiologies where you might have a
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vasculopathy in a child, a juvenile rheumatoid
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arthritis patient, for example, HIV is another.
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There are a lot of infectious etiologies that
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are different than atherosclerotic disease, which
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is what we would normally suspect in an adult.
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So this patient did have, uh, perfusion imaging
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and it showed a matched defect to the DWI sequence.
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These are not in color, but they show that there was
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the same area of involvement as the DWI and therefore
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there was not salvageable tissue in this individual.
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