Interactive Transcript
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Let's start with the first case.
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It's a multiple myeloma patient.
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You already saw the cases, so there's nothing blinded
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Or anything.
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Um, this is, um, this was a multiple myeloma patient
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coming for, um, initial staging.
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Um, as you see here in this patient, um, I,
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as I always tell my, um,
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and again, I'm not gonna go through my search pattern today.
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Um, we're just going through the findings.
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Uh, so I'm not gonna go systematically,
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although I always go systematically when I, when
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I look at my cases, um, as you see here,
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we starting there is finding here for collectivity
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and, um, I'll put it in a, in a bone window.
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There's a litic lesion here in the skull.
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And if I put it in a soft tissue window,
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you can obviously see that there is a soft tissue component
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that is extending out to thecal,
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but also it has, um, an extra axial
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and intercranial, extra AAL extension.
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I will put it in a brain window.
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It's not the best brain window you can have.
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'cause the CT here is like a one kernel ct.
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So it's not the best CT for the brain, right?
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It's trying to manually make it there.
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It's not helping much. This is the best I can show you.
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But see there is here a soft tissue component
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that is extending intracranial,
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but I think it's, look, it's obviously extra axial, right?
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So there's a soft tissue component of that lytic lesion,
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which, which is typical for multiple myeloma, right?
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This is the first one,
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and I can show you the, let's put the volume of interest
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here, right?
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Like I told you before, for clinical use,
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you wanna make your volume of interest the biggest you can,
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but make sure that you're not including something
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that might be hotter than your lesion.
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Because we report the max UV, right? The SUV max.
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So I'm gonna take it away from the cortex
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because the cortex might be hotter than my
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lesion, although I don't think so.
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But see, I'm scrolling up
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and down, making sure that I'm not touching the cortex
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and oh, I always can go corona
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and to make sure that I'm out.
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It's kind of 7.9 near the max SUV, right?
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You, you notice that I have in mind I can display more.
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I have the peak, the means and the vision.
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I have others, but we report in the clinical report,
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the max, the SUV max, right?
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I'll go down more in the axi.
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You always have to look at the brain.
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Like I said, I'm not gonna go systematically,
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but quickly through
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the pet only image, which I always depend on a lot,
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all you see is basically
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skeletal findings.
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See here and this rep, right?
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Yeah. So you guys can see it.
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I, I know that you guys went through these cases.
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These were last weak cases.
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Again, it's a,
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it's a bone lesion with a soft tissue component.
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Ative, some areas it's a,
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it's an obvious litic destructive lesion
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of the soft tissue component.
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In other areas, it's more of permi, right?
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This most eaten how you describe it.
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See here, you have to zoom in to be able
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to see the abnormality, the bone abnormality you see here,
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it's not the obvious litic destructive,
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but it's obvious that the bone is abnormal, right?
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So really this is a bone lesion
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with a soft tissue component.
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It's not a subpleural or pleura based, um, lesion.
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It's not a long lesion. Let me put it in a long window here.
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So look here. See, it's not a long nodule. It is not.
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It is actually a bone lesion with soft tissue component.
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And this is important to determine in a multiple myeloma.
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Why? Because multiple myeloma lesions are either middle
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or extramedullary lesion.
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And it's important to decide on this patient,
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are all these lesions gonna be middle only or there is mid
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and extra medullary?
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This is important in their staging.
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And it's, so Im important to emphasize this
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and I, I always tell that to my president
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'cause they always do this mistake.
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They still use primary
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and metastatic terms in, um,
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myeloma and in lymphoma.
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And these are the two that we see a lot.
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We don't see leukemia a lot in our, uh, pet suite
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because leukemia is considered low grade for us.
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So re rarely we would see them coming through our suite.
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Um, so what is the point I'm making here?
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I'm making the point that
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primary metastatic disease are not valid terms
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in lymphoma and myeloma.
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And you have to think about it for a second.
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If you think about myeloma, what is the primary site?
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And if you tell me, well,
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bone marrow is the primary site, okay?
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Bone marrow is the primary site.
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What is the metastatic site? In the myeloma disease?
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There's no metastatic, right?
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Because hematologic malignancies are different than
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the rest of malignancies.
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There's no primary metastatic.
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So they have, we, we have our own terms when we talk about
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hematologic cancers.
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So we need to use their terms, right?
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So the terms we use here in myeloma is medullary, intary,
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and extramedullary, right?
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Or medullary and extramedullary patients.
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Um, in lymphoma we use nodal and extra nodal disease, right?
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So just use their terms in your reports.
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Never say primary metastatic disease.
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When you talk about, um, a myeloma patient,
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a lymphoma patients, even if it's a negative scan,
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don't say, okay, there is no f dg avid primary metastatic
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disease in the myeloma or lymphoma patients.
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It just doesn't look right
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and it makes you look like you
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don't understand what you're talking about.
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This is my advice, okay? So coming back to the patients.
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So in, in a, in a lesion like this, it's easy
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for you when you're looking like on, on, um,
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on the point in the long window
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or the soft tissue window to say, okay,
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is this a pleural based nodule?
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Don't look carefully
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because this will put it in an extra medullary lesion
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category and this will stage the patient differently.
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So make sure, and in this lesion too, make sure that,
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is this a bone lesion or is this really a long lesion?
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Okay? Again, this is another
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litic lesion, right?
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And like I said
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before, you already went through this whole patient,
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the whole case,
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and you just figured out that all these lesions are
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just here.
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Look how here, put this one here. TIC lesion here.
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That is ly active. This is the uter.
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You have to make sure it is the uter. Just follow it up.
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This there, right? So this isn't, there's no problem.
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It's not a lymph, it's just David.
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So all the lesions in these patients are,
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um, bone lesions, right?
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I'm looking at bladder
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and there's nothing suspicious here.
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It's just like some, um, bladder neck funneling
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that we sometimes see or there's maybe, I don't remember.
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There's something in this.
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I'll just go slowly and make sure what are we seeing?
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Because there's some budding here
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and the, it's just how the most probably it's how the
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bowel is sitting on the semi empty bladder.
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Just put it in a different orientation and go there.
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I'm sorry it's a little bit slow
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because I have like four cases open.
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So single here is gonna be slower than normal.
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See how, how it is looking in the sagittal, see this
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here, the in the bowel is sitting on the bladder,
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making the bladder look kind of concave, right?
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This one, this is why when you look axial,
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it looks like there's focal connectivity here,
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but it's not focal connectivity, it's just
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the bladder, right?
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You just confirm that this is what it's, okay.
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So this lesion, this patient has numerous metabolically
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active medullary,
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but plate lesions with soft tissue,
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some are some which is the larger,
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larger ones have soft tissue components.
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All this has been lower disease, right?
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And then some incidental findings, right?
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And I'm not gonna go over the incidental findings.
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You know how to report incidental CT findings
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and we do report the CT findings, of course.
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Um, the important other point I always make in these cases
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is that there's no evidence
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of metabolically active extramedullary disease.
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This is it because this is important in the stage.
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That's it for this multiple myeloma patient
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because this was an interest staging, um, patient.
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And of course if you look here at the map,
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although there is diffuse in this patient,
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there is diffuse bone marrow activation as you see here.
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There's diffuse homogenous bone marrow activation,
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but it's obvious that is in the, there's a background
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of bone marrow activation, but there's also disease, right?
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It's obvious. This is what we always say.
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We can tell when there is a bone marrow involvement on top
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of the bone marrow activation, right?
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So there's a difference between the look of involvement
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or infiltration and activation.
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There's a difference. And we can tell when there is
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both in the same patient.
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And you can see here how there is bone marrow activation
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and infiltration in the same time, right?
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It's obvious in this patient, right? It's beautiful, right?
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I don't think there's anything else in this patient that is,
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um, significant.