Interactive Transcript
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So let's talk about approach.
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We all wanna get to the diagnosis, right?
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And in a lot of, uh, musculoskeletal radiology,
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we're accustomed to looking for the primary finding.
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We're faced with a clinical question like, uh,
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ligament tear, right?
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And so we go right to the anatomic region
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and evaluate the ligament itself and try
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and determine if it's in continuity or not.
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The problem with doing that in nerve imaging is
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that the nerves are very small,
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and in some cases, even when there are a very convincing
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clinical picture and EMG findings, uh,
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to suggest a nerve abnormality, it will look for all intents
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and purposes completely normal on MRI.
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And so this is actually a pretty tough place
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to start when you're identifying these cases.
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And one thing to keep in mind is
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where we're really gonna help the surgeons is in
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identifying an underlying cause.
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So we'll come back to that. So probably a better place
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to start when you, when you look through the MRI
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of these cases is for those secondary imaging findings.
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And what the secondary findings are predominated
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by are muscle abnormality.
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So remember, the muscles are really kind
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of the end unit of those nerves.
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Uh, when the nerve is injured,
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those muscles undergo changes in a
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pretty characteristic way.
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Uh, so we're looking for those
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signal changes within the muscle.
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Bare bellies, much bigger realistic, right?
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Easier to see on those axial sequences.
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And then secondarily, we need to understand those patterns
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of involvement so the individual nerves have
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different distributions.
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And so understanding the distribution
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of muscle involvement really helps guide your search.
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So once you've screened these cases,
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you identify the muscle abnormality
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and you say, Hey, this looks like a radial nerve
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distribution, then you can go back
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and look at that radial nerve itself, try
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and find the underlying cause or potential abnormality.
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But I'll tell you one secret to these cases,
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and that's most of the information
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that you need is right here in the clinical picture.
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So these cases in particular,
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I'm really delving into the chart.
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I wanna know all of the clinical manifestations,
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the chronicity of, um, of symptoms in these patients.
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The physical exam findings, a lot
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of time you get supporting information
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before you get imaging.
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So you'll have EMG findings as well.
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Uh, and by the time the patients come for MRI imaging, uh,
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they've been evaluated typically by a subspecialist, uh,
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whether that's a specific to nerves or to surgery.
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Um, they will have a general idea of
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what the abnormality might be.
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So MRI is really helpful in confirmation
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and again, identifying those underlying causes
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of potential entrapment.
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We're really trying to help guide
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the surgeon in these instances.
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Is this something that can be intervened upon?
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Where is the abnormality so they know where to search, uh,
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where, where to start their kind of surgical approach.
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So start with that clinical information.
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Really gather as many clues as you can.
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And then when you start looking at the cases,
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look at the muscles first.
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I really like those axial sequences.
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You can kind of quickly scroll through a stack
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and see if you can see any of that denervation change.
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Um, if you do try
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and identify, is that a pattern? Is it a single
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Nerve distribution or is it multiple?
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And then if you identify a single nerve,
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then you can go back and look
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for those primary abnormalities of the nerve
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and then try to identify
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that underlying cause we can wrap it up nicely in a package
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and, and send it back out, uh, to the medical record.
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So, uh, as similar to our approach, let's talk about some
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of these secondary findings.
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So again, we're looking at the muscles
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and we're looking for that denervation change
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and it progresses from our acute findings, which can occur
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as early as 24 hours after nerve abnormalities.
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So nerve injury, um, is usually the best example in
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how they determined that.
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You could see muscle signal changes that early on.
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Uh, then they kind of progress into this subacute phase,
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which has a variable length of time, depending on
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what you read before we really get into the chronic changes.
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So early on in that acute phase, it's what you might expect.
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We see edema, we haven't lost any
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of the muscle volume at this early phase.
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In fact, sometimes the muscles are a little bit enlarged,
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but we're looking for that increased signal on
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fluid sensitive sequences.
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And in the chronic phase, we're looking for
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that fatty replacement, that infiltration of the muscle
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and overall volume loss.
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Once you get to true chronic, uh, fatty infiltration
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of the muscles, you really lose any T
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two signal abnormality.
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So don't be surprised to see a complete absence of, uh,
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T two signal abnormality
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and, uh, a large presence of fatty atrophy and infiltration.
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And primarily when we're identifying, uh, the course
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of those nerves, we wanna check to make sure
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that there isn't any abnormal angulation.
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We're looking for mass effect, kind
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of moving the nerves away from their normal course.
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Uh, any abrupt changes as well in kind of the,
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the typical anatomic, um, course of the nerve is gonna be
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concerning for abnormality.
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And then next we wanna check the nerve caliber.
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So this is where those axial sequences are really helpful.
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You can kind of compare, you know, one axial slice
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to another is the nerve all of a sudden getting larger.
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Uh, you can also have decreased size
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of the nerve in some instances
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that is more chronic injury to the nerve.
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And finally, signal abnormality.
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As we can see in this image
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of the elbow here in the bottom right, we have some areas
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where, uh, there's increased signal in the nerve.
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It's pretty hyper intense in this instance.
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And you can see these individual
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fales identified by the blue arrow.
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Those are enlarged. They kind
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of have variable size in this instance.
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And one trick that's great, uh, about nerve imaging
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and what I would recommend you to do on any case
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where you have, uh, images of the nerve,
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which is pretty much every joint that you'll image in M msk,
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is look for the normal nerves
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and identify what their typical signal is.
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So we have great comparison in this instance.
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This is the median nerve compared
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to our abnormal ulnar nerve.
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You can see that the nerve itself is relatively iso intense,
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maybe a little bit hyper intense to the muscle,
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but certainly not approaching that fluid intensity signal
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that we see here in the ulnar nerve.
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Um, because there are often multiple nerves in
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the same axial slice.
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You have this great kind of internal comparison.
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Internal control of normal, uh,
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can be really helpful when you're evaluating these cases.