Interactive Transcript
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Dr. Laser,
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this is a 59-year-old woman with blurred vision.
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We're not really in the visual area at all.
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We're up high in the frontal region,
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involving the middle and,
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to a lesser extent,
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the inferior frontal gyrus,
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and we have a mass here that looks extra axial,
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doesn't it?
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Correct.
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It's got a very,
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very sharp interface with the underlying brain parenchyma,
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and it's interesting that it does not
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generate much, if any, vasogenic edema.
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There was also a curious-looking area of tissue
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thickening around it that looks separate from it
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that that may be some additional
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tissue in the dura.
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It may be a small hemorrhagic or proton
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suffusion or it may simply be tumor.
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We don't have a contrast enhanced study.
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If I had to bet, I'd bet on tumor.
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And the reason I would is because it's still gray
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over here, it's not fluid like on the T two.
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So I like it a lot for just a strange
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continuation of the same lesion.
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And then when you look at the calvarium,
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the diploic space signal is just completely
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wiped away on the T one.
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I like to have a true T one in almost every
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skeletal study that I ever do. Now,
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granted this is a neural study,
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but there's a skull here involved
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and that is sket at all.
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So I like a true t one as opposed
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to opposed to a proton density,
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and look at how thick the calvarium is.
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And then on the outside of the calvarium,
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we have another layer.
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So this is like an incredible club sandwich.
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You know, you've got the Galia,
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you've got the outer table here and on top of
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the outer table, subgaleal is this mass.
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You've got the diploic space which is abnormal.
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You've got the inner table which is thick and
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you've got a band-like area of tumor and then
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you've got a lentiform area of mass and or
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tumor and then you've got the brain.
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So that's how I would dissect the signals.
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In this case, it's a low field study.
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The patient moved a little bit but still
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the teaching is there axial T one,
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axial T two coronal flare.
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So the take-home message here is what
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do you do with this lesion?
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What's the differential diagnosis?
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And let's throw out some differential diagnoses.
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I mean, I would, you know, I would consider,
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you know,
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something like a primary bone tumor of the skull,
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including a sarcoma.
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I'll start out with some weird things like sarcoid
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and even tuberculosis. And you know what I like,
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especially when I have very gray signal.
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Not a lot of high signal because there's
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not a lot of cytoplasm in lymphoma,
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seeing lymphoma do this and kind of sweep
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its way right across the calvarium.
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And even though it wipes out the calvarium,
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it's surprising how little surrounding
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reaction it generates.
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What are some other things
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you would consider here?
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What would you think about a Chloroma in this
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case? I'd like Chloroma a lot. The only,
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the only thing I would say is,
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uh I wrote the first Chloroma paper,
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an MRI back in 1990 in the Jurassic period is that
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they're kind of, they're kind of nodular,
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they're kind of round. They tend not to be,
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not to be flat but,
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but they are bulky and they come from patients
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that have acute myelogenous leukemia.
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So they're nests of myeloid cells
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and that could occur at any age,
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any age that you can get AML you can get
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a chloroma. So that's a great thought.
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Anything else? So look all things being common.
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One thing that I would consider
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obviously extra-axial lesions,
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men would be included in there and then down the
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spectrum of aggression of meningioma
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all the way to Parma. Yeah.
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And hemangiopericytoma used to be
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in the family of meningioma.
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It was considered kind of the ultimate aggressive
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meningioma in the type three category. Now,
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it's been reclassified as a fibroid
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tumor all by itself.
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But let's talk about meningioma types
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while we're at it. You know,
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you've got the grade one meningioma,
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which is meningioma.
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the fibrous or fibroplastic type.
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More common in the skull base and sphenoid
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transitional mixed simo angios microcystic
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secretory lymphocyte-rich and metaplasia and some
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of these may generate exuberant vasogenic
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edema as we've discussed before,
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due to the production of the vascular endothelial
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growth factor. Grade two. Fortunately,
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there aren't as many there to memorize.
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There's only, there's only three.
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And what are those typically clear cell
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cordo and then atypical by histology.
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And then you know,
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those will behave a little more aggressively.
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It's not possible by MRI to select
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out the individual histology.
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But it is possible to say if it's low grade or,
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or high grade,
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grade three and the grade three ones,
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what are theologies there?
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Papillary and also anaplastic,
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right would be your grade three.
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And then they used to say hemangiopericytoma,
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they would grade that as either a two,
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a low grade hemangiopericytoma or a three.
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And as we said,
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that's been taken out of the Meningioma World
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Health Organization grading system,
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which we just gave you and it's been reclassified
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as it should be in the musculoskeletal
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tumor group, the fibrohistoid group.
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So this is an aggressive lesion.
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We've given you an extensive
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differential diagnosis.
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I left one thing out actually one very important
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thing and that is melanotic lesions of the dura.
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They're kind of gray. They may be pigmented,
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they may not when they are pigmented,
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they're pretty dark on T two.
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They're intermediate to bright on T one.
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You can not only have melanoma of the dura,
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you can have melanosis or hypermelanosis of ito.
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And that's one that people often overlook and
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the melanoma lesions are very aggressive.
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They go through bone.
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So that's got to be in your
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differential diagnosis.
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Whenever you have one of these lesions that's
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going from one compartment to the other and
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destroying the calvarium or skull. Let's move on.
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Shall we, Lazar? Out, out, out?
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