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Imaging Modalities

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Okay, so imaging modality.

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So in the neonate, um, we often start with head ultrasound

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because it's, um, you know, there's no ionizing radiation.

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It's fast bedside exam.

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And so, uh, they can go through various fontanels,

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which are essentially these know, like open, uh, you know,

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non ossified, uh, fibrous things, um, in the skull, uh,

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that actually the sutures and fontanels are there

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because they can mold as the baby goes

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through the birth canal, right?

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So you have some level of plasticity,

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and then as the brain grows, it keeps the sutures open

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and they start to, uh, narrow

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and fuse over time, depending on age.

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So the anterior fontanel actually stays open, you know,

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till about 14, 18 months of age.

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So obviously throughout the infancy you can

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still intonate through it.

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And so you can see in the coronal

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and the satchel plane, um, the ventricles,

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nice gray white distinction here, the corpus callosum, uh,

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the cerebellum, if you're lucky as well.

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We don't typically do ct, you know,

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because of the ionizing radiation,

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but let's say if there's a trauma, right?

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Accidental or, um, non-accidental, um, any concern for, um,

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you know, uh, hemorrhage, for fracture, um, rapid screening,

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if, uh, MR is not immediately available,

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that might be within the risk benefit ratio.

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And so here, uh, you can see that the neonates have, uh,

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water or brains in adults, right?

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Because they're not myelinated yet.

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And so it is, uh,

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a little bit more hypodense here, and that's normal.

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And the overall volumes are fuller too, right?

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So unlike the, the atrophy you see the adult brain, right?

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You, you actually have a relatively smaller, uh,

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ventricle subarachnoid spaces for, for much

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of the infancy childhood.

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Now you can have the, uh, so-called benign enlargement

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of subarachnoid spaces, transiently in around nine months

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or so in self resolving around two or three years,

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but, uh, not in the neonate.

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And then you have these sutures, right, the sutures

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and fontanels that I mentioned.

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So these are gonna, um, gonna be pretty open and,

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and maybe a little overlapping if, uh,

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they had a vaginal burst, right, going

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through the canal there.

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Uh, and then they, they actually narrow pretty rapidly in

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the first like month or so.

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So then you have like a couple millimeters,

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and then they steadily, uh, narrow over time

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and have different, uh, age related times of closure.

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So for example, the atopic suture in the frontier, uh,

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closes earliest, uh, it can be, you know, four months

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or sometimes even a little bit earlier.

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And then we have mr, which is really the workhorse

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for all of our problem solving.

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So I wanna show you this, uh,

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because this is what a normal, uh,

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term neonatal Mr should look like, right?

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So I have these arrows here on

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what are called the posterior limbs of internal capsules.

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If you've got the, you know, anterior limb,

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the Gen U, the posterior limb.

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And so you see that that's pretty much the only part

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of the neonatal brain that's myelinated, right?

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Because what do you have to do when you're born?

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You have to cry and reach out for mom,

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and that's pretty much it.

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So, uh, this T one shortening myelin is fat

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and protein, right?

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So you're gonna get T one bright,

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T two dark, uh, kind of signal here.

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And so it's pretty much that, uh, posterior third

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to posterior half of the IC

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or the click, uh, should be myelinated.

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If you're a full term infant.

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Obviously if you're preterm, it might be a little less,

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but if you're not seeing it at all or barely, then

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You, you have to be suspicious that maybe there's

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something obscuring it, right?

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Like, um, maybe an edema from an, uh,

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hypoxic ischemic injury.

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And so here, this is the,

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the apparent diffusion coefficient map from the diffusion.

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Um, and so there's nothing restricted

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that's as it should be, right?

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This is a perfusion, uh,

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what we call arterial spin labeling.

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And so you see that again, right?

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The basal ganglia are the most robust, um,

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and the corticospinal tract.

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So they have good flow

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because they're actively developing as a result

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because they have more flow.

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Normally, if you have a hypoxic ischemic insult,

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they will be selectively vulnerable to a severe, um, HII

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because they are taking more blood flow baseline,

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but still the rest of the brain does have,

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you know, a reasonable flow.

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It's just not as much as the actively

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developing myelinating areas.

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So that's important too. And then Mr.

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Spectroscopy another advanced tool, right?

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So we can do voxels,

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usually they'll do one over the basal ganglia,

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like a single voxel one over the, uh, white matter.

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Um, and then you can basically get

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the different metabolites.

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This here is a long echo MRS,

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and so we're just cleaning up the baseline here.

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Essentially just looking at the major metabolites.

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And so again, in contradistinction to adults where they have

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that hunter angle that's supposed to go up, right?

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So your NAA from your neurons is higher than your

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choline from your cell membranes.

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Well, the infants are still, you know,

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they have some anaerobic metabolism, even more

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of their preterm, but basically at term age, right,

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they still are undergoing a combination

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of aerobic and anaerobic.

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So the NAAP, uh, area under the curve of the NAA peak,

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right, is around like two thirds of the choline.

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And that's actually normal to have that slight down slope.

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They can have a little bit of lactate

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and lipid again because of that.

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Um, some of that physiologic immature in heric metabolism.

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So that's actually what a normal MRS looks like,

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and that'll be important for us later on.

Report

Faculty

Mai-Lan Ho, MD

Professor and Vice Chair of Radiology

University of Missouri

Tags

Vascular

Ultrasound

Trauma

Perfusion

Pediatrics

Neuroradiology

Neonatal

Metabolic

MRP

MRI

Infectious

Iatrogenic

Drug related

Congenital

CT

Brain

Acquired/Developmental