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Brain Pathologies in Premature and Term Infants

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So when I'm reading a head ultrasound,

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I want to know the history.

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If it's a preterm infant, I'm looking

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for germinal matrix hemorrhage, encephalopathy

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of prematurity, things like that.

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In a term infant, I'm focusing on other findings

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and an infant who's over the age

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of 34 weeks gestational age.

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The likelihood of germinal matrix hemorrhage is much lower

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and so we're looking for typically other, uh, abnormalities

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to, to answer or screen for in those infants.

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So a reminder of the papilla grading

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of germinal matrix hemorrhages in premature infants.

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So a grade one germinal matrix hemorrhage will be hemorrhage

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that is confined to the coth thalamic groove.

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Grade two, you have intraventricular extension without

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ventricular magaly.

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Grade three is where you have intraventricular hemorrhage

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related to germinal matrix hemorrhage plus

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ventricular magaly.

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There can be some confusion

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between post hemorrhagic hydrocephalus

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and grade three germinal matrix hemorrhage,

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especially among my residents.

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So in order to call it a grade three germinal matrix

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hemorrhage, it has to be a at the time

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of presentation of hemorrhage.

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So, um, you have germinal matrix hemorrhage filling the

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ventricles plus ventricular mely at the time of diagnosis

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on follow-up studies.

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We'll talk about post hemorrhagic hydrocephalus in a little

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bit, but the blood itself can cause ventriculitis and lead

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or plugging of, uh, of the cerebral aqueducts.

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And then you can get subsequent, uh, hydrocephalus.

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So grade three is when you have blood plus dilation

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of the ventricles at the time of presentation of hemorrhage.

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Grade four germinal matrix hemorrhage is not called grade

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four germinal matrix hemorrhage anymore

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because they used to think it was blood extending

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through the append of ventricular lining into the

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periventricular white matter.

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And we now know that that's not the case.

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It is a per ventricular hemorrhagic venous infarction,

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so not blood extending through the append lining.

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Most of my NICU colleagues still want us

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to say grade four germinal matrix hemorrhage just so

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that they can kind of fit the, um,

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infant into their carrying algorithms.

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But they also understand

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that it's now a more appropriately called periventricular

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hemorrhagic venous infarction.

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Um, so an example of what that looks like,

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so not grade four germinal matrix hemorrhage,

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it is now periventricular hemorrhagic venous infarction

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where you have that abnormal hyper echogenicity related

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to venous hemorrhagic infarction in the

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periventricular white matter.

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And again, just a reminder of why this happens.

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You have these teeny tiny like thread like venous structures

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that with a little bit of blood pressure

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or heart rate instability, you can get venous stasis

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and that leads to hemorrhagic venous and infarction.

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So, uh, formally known

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as grade four germinal matrix hemorrhage, periventricular,

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hemorrhagic venous infarction is what we call

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that more appropriately these days. It has a

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Typical appearance as that blood ages over time.

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And this patient unfortunately is a nice example

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of us following that, uh, evolution

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of the hemorrhagic venous infarction over time.

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So at the time of, uh, acute presentation,

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the per ventricular white matter will be hyper coic, um,

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at the side of the hemorrhagic venous infarction.

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Over time, encephalomalacia develops

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and that, uh, echogenic focus will turn into a

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hypoechoic focus and then it will become anti coic as

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that blood evolves over time as that evolution occurs.

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Typically that cystic space will communicate

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with the lateral ventricle

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and that's when it's called the po and cephalic cyst.

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So you can see this abnormal, uh,

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cystic structure communicating

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with the frontal horn lateral ventricle

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as a po and cephalic cyst.

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I wanna distinguish that from post

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hemorrhagic hydrocephalus.

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So, uh, post hemorrhagic hydrocephalus results typically

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from germinal matrix hemorrhage.

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The hemorrhage irritates the

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ventricular or epidermal lining.

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It plugs up the arachnoid granulations

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and impedes reabsorption of cerebral spinal fluid.

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And then you might also have hemosiderin

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or clot physically blocking the flow of CSF.

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So a reminder of the normal flow of cerebral spinal fluid.

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Um, it goes from the lateral ventricles

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down into the cerebral aqueduct

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and this is the most common location where blood, uh,

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will physically cause an obstruction

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of the ventricular system.

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So it's kind of a multifocal multifold process going

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on in these infants.

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Um, this is an, uh, an example of an MRI

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where you can actually see

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that low signal hemorrhage blocking that cerebral aqueduct.

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Um, we can see that in infants that ultrasound

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and we will follow the size of ventricles over time.

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Um, a couple of words about encephalopathy of prematurity

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or white matter injury of prematurity.

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Uh, this is, uh, like a watershed type infarct

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that happens in extremely premature infants.

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It's in the per ventricular location.

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The location is classic, so at the frontal

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and posterior aspects of the lateral ventricles,

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the periventricular white matter, um,

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normally your periventricular white matter

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after one week of age will be less echogenic than the

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adjacent choroid plexus.

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Um, I will show you an example on the next slide about

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what we call flaring.

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So prior to one week of life, you may have this, uh,

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normally hyper coic appearance, especially

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of your posterior parietal occipital white matter in the

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per ventricular region.

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So this is the same infant who was, um, imaged twice,

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once on day of life, one for concerned

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for intracranial hemorrhage,

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and then we image this infant one week later

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and look at the echogenicity

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of the posterior per ventricular white matter on day

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of life one compared to, uh, after one week of age.

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So it's the same echogenicity

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as your choroid plexus prior to one week of life.

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After one week of life it becomes h hypo coic compared to

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that choroid plexus.

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So just be careful calling, uh, white matter injury

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of prematurity prior to one week of life.

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You don't wanna call normal variant flaring, hyper genicity

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a word about the extra axial spaces.

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So especially when we are looking at our mastoid view at the

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posterior fossa or when we are looking at the subarachnoid

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and uh, subdural spaces at the vertex, a reminder

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that the subdural space is a potential space.

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So we don't typically see the subdural space

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unless something is abnormally located in

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that subdural space.

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Our, um, text part of our protocol will get, um,

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magnified images of the extra AAL spaces at the vertex,

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looking at the subarachnoid versus subdural space, looking

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for any abnormal collections to distinguish

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between the subdural space

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and the subarachnoid spaces to look

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for either a subdural collection or subdural hemorrhage.

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Um, we are looking for a couple of things.

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Number one, we don't wanna see any displaced arachnoid

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monitor, so we want to be able to see the, uh,

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bridging veins and arachnoid granulations extending from the

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surface of the brain all the way to the inner table

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of the calvarium.

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We don't wanna see any displacement towards the brain

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parenchyma and we definitely don't wanna see any

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displaced arachnoid matter.

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So here is an example of that.

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So this was an infant who, uh, has subdural collection,

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so pay attention to a couple of things.

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Um, on this ultrasound,

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this white arrow is showing you displaced arachnoid mod.

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So typically this arachnoid mater is pushed all the way up

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to the inner table of the calvarium.

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So we don't actually see this structure.

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So this purple arrow is pointing to the subdural space.

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There's some, an coic fluid pushing

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that arachnoid monitor down towards the brain.

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When if we were to put color doppler imaging on,

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we would see vascular structures extending only

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to the displaced arachnoid matter, not all the way

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to the calvarium, which we would like to see.

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So that's what this blue arrow is pointing to on MRI.

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We can see this, um, on T two weighted sequences,

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but it has to be, uh, like a, a super fluid sensitive

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MRI sequence to be able to see that level of detail.

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So again, the white arrow on the sagittal uh, cysts

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or fiesta super T two weighted sequence, you can see

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that wide arrow is pointing

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to the displaced arachnoid monitor.

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We see, uh, bridging veins displaced towards

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the brain parenchyma.

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Normally they should extend all the way to the inner table

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of the calvarium and the purple arrow is pointing to

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that subdural space.

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So this is a subdural collection in an infant.

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This patient for some reason, the clinicians

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before they got the MRI got a ct,

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which does not give us the level of detail that we need.

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So a reminder that an infant's

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optimal imaging is either ultrasound or MRI.

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Uh, so head ultrasound is for screening, MRI is

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for diagnosing, um, in much greater detail

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'cause we can see much better and we can see signal changes

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of ischemia and hemorrhage, et cetera.

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Um, CT is really not, not great

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unless your only question is,

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is there hyper attenuating hemorrhage And compare

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that example to this case.

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So this is a case of benign macro cranium infancy

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where the extra axial spaces at the vertex are large,

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but we see bridging structures extending all the way

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through these extra axial spaces.

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So this blue arrow is showing you a bridging vein extending

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through that subarachnoid space.

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So we have those structures going all the way from the

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surface of the brain through the inner table

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of the calvarium, and we also don't see any displaced

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arachnoid moderate in this infant.

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I also wanna point out that this is a specific

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patient population.

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So benign macro cran of infancy is a normal finding.

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These patients typically have big heads

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and if you look at mom

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and dad who are in the room with you, um, one

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of them will typically have large head

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circumference size as well.

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So these are infants who are typically six

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to nine months of age.

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They have a totally normal neurological examination.

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If you have an infant in the NICU

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who is younger than six months of age

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who maybe was premature and has been in the NICU feeding

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and growing for their entire life,

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that is not gonna be benign.

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Macro cranium of infancy.

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If you see large subarachnoid spaces in those infants,

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that typically is gonna be a level of atrophy, um, related

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to, um, their prematurity.

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So in summary, uh,

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most germinal matrix hemorrhage occurs

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within one week of life.

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And that is why we typically do screening head ultrasounds

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at one week of life.

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We want to see most of the cases of hemorrhage

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that are gonna occur and then we'll do screening head

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ultrasound again at about four to six weeks of age.

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And then at term equivalent

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or the time of discharge, a reminder that grade four

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germinal matrix hemorrhage is no longer

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actually called grade four germinal matrix hemorrhage.

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The more appropriate term is periventricular

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hemorrhagic venous infarction.

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There are a lot of normal variants

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that we can see at head ultrasound, especially flaring

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and don't call that pathology erroneously.

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Make sure you pay close attention to the extra axial spaces,

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subarachnoid versus subdural space.

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And if you can see a vascular structure,

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make sure you interrogate it with color doppler.

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Or if you have a machine with some sort

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of microvascular imaging, um, like a B flow

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or a superb mi microvascular image, um, make sure you use

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that to ensure vascular patency.

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With that, let's go on to several examples

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to illustrate some of these things that we've just learned.

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Text

Faculty

Judy H. Squires, MD

Associate Professor of Radiology

UPMC Children's Hospital of Pittsburgh

Tags

Ultrasound

Pediatrics

Normal/Normal variants

Normal Anatomy

Neuroradiology

Neonatal

MRI

Brain