Interactive Transcript
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We've got a 54-year-old woman,
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presents with bilateral foot drop
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and dragging both feet for six weeks.
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That's not a very specific history.
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But yet, it does tell an important story.
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Certainly, something happening with the cord or the spinal
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canal affecting the cord.
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And I'm here with my colleague,
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fellow neuroradiologist and expert, Ben Lazar.
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And we're looking at this gal's cord on a sagittal T2.
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On your far left, no fat suppression added.
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In the middle, we have a contrast-enhanced T1,
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and on the right, we have a modestly fat
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suppressed contrast-enhanced T1.
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That's probably the most impressive of the images,
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but we both know the diagnosis.
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But I'd ask you to zero in on what bothers
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you about the Sagittal T2.
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So, two things on the sagittal T2 bother me.
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One,
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there's this vague increased signal
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within the spinal cord.
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Essentially, lower thoracic spine that is ill-defined.
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It has no mass effect.
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It's not expanding the cord.
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The cord is still normal in contour
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and shape. Most people would blow by that,
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don't you think? I think so too.
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It's very subtle when you correlate it with the other
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images, sure, it makes it a little easier.
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So the Sagittal T1, and this is admittedly difficult,
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but when you really window it and you administer contrast,
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there is a faint blush of enhancement,
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especially right there.
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Again, that is another finding that you
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could completely blow over.
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And it's totally explainable why 34567 MRIs are done on
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this patient and nobody comes up with an explanation.
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Making matters worse is look how big the field of view is.
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So you might be looking for tiny little peel vessels,
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as in a Dural AVF.
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Now, you're probably not going to miss a type two intramedullary
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dural AVM because those are easier to see with flow voids.
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But dural AVFs, they're tiny.
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They're less than a millimeter in size.
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So when you have low-res imaging or large fields of
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view like you usually have with a thoracic spine,
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you're going to miss the abnormal vessels that are seen in
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the intradural space. Now, we shunt over here to our,
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pardon the pun shunt.
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We shunt over here to our axial contrast
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enhanced fat suppression image,
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and we've got this funny little owl's eye sign.
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In fact, it looks like ET.
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The extraterrestrial there are the two eyes of ET right
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there, and the shape of the head is pretty good.
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So now that we see that the lateral column has abnormal
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enhancement, we're confident that we have an abnormality.
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So beside provides a vascular abnormality,
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like a type one dural AVF, which is the most common.
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70% of all of them.
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What is in our differential diagnosis?
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Let's just tick down the differential.
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So pick one. One demyelination.
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Demyelination, okay, let's talk about that.
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What goes against it?
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What goes against it is typically demyelination is going
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to be peripheral wedge-shaped along the cord,
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typically dorsal spinal cord. In this case,
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it's more central, it's more lateral enhancement.
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But on the T2,
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you can see that the abnormal signal is pretty
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much within the center of the cord.
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And skip areas, too. And skip areas.
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What about a viral myelitis?
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That comes up a fair amount.
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Somebody sees a high signal in the cord.
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I've been a trained radiologist for longer
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than I care to acknowledge.
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Usually, the first thing that comes out of their mouth is,
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well,
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I can't rule out, but then they say can't rule out
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myelitis, and it's just something familiar to them.
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And then I ask them what kind of myelitis?
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And they usually say, well, viral or infectious.
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So
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would a viral myelitis or any kind of
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infectious myelitis even fit here?
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Probably not typically infectious myelitis.
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A, the enhancement pattern is going to be different,
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and B,
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you're going to see more expansion of the cord and
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the length of the lesion is going to be yeah,
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it's usually not so far up.
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The cord is often swollen.
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Admittedly, the enhancement pattern is pretty variable.
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But another key thing is somebody with a myelitis that's
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infectious. It comes on like, really acutely.
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And this is a condition that gradually, gradually,
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slowly ascends and produces lower motor neuron signs.
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So clinically, they don't look alike at all.
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And that is also true of the toxic myelidities, too.
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You can get it from toluene and heroin and valproic
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acid and a bunch of other toxins.
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Lead, even porphyria, is in a way,
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a toxin that results in a myelitis.
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So it doesn't really fit for a myelitis.
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Now, you do get cord signal alteration,
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gliosis and myelomalacia from DJD, but that one's easy,
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right? We don't have DJD, we don't have cord compression,
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so we don't have signs of arterial insult.
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Then you get into something like diabetes mellitus,
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severe small vessel disease.
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That can be a real difficult one to exclude.
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More often than not, though,
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they have really severe peripheral neurologic dysfunction.
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And I haven't seen that many cases over my lifetime
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of diabetes predominantly affecting the cord,
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and it's not a long level abnormality.
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What about Guillain-Barré syndrome?
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So Guillain-Barré syndrome, typically you would see,
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especially on the post-contrast images,
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really bright cauda equina nerve roots,
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and it typically ascends from the cauda equina to the head.
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You would see the cauda equina nerves being enhancing,
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and then the spinal cord from the conus extends.
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Ending up, and in this case, we don't really have that.
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It looks like it coats the surface of the cord.
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It's kind of weird-looking.
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And Guillain-Barré is mostly motor.
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It gets into the respiratory system, and you
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got to put the patient on a ventilator.
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But there is a sensory form of Guillain-Barré
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seen about 5% of the time.
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These patients are also motor patients,
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patients with Dural AVFs,
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although eventually they do get a sensory level,
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but the appearance is not consistent.
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Even though you do have this filmy pattern of enhancement,
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it's a little more intense with Guillain-Barré and
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as you said, nerve roots from the bottom up.
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And this one is right about at T nine,
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which is probably the most common site where you're
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going to see the epicenter of a Dural AVF.
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Then we've also got these lateral areas of enhancement
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on the axial fat suppressed image,
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which is not typical at all for Guillain-Barré syndrome.
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One of your colleagues mentioned subacute combined
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degeneration with deficiency of vitamin B twelve
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pathway. That can give you an Alzheimer's,
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but it is a posterior column disease,
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so it's usually more in the back.
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And they don't have this uber long pattern of involvement.
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The enhancement is scant to none,
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and it's an easy diagnosis to exclude by laboratory
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methods. I think we'll stop right there,
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unless you have any other thoughts.
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No? Great. Thank you.
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