Interactive Transcript
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So, Dr. Finazzo, now that we've established we've
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3 00:00:02,740 --> 00:00:05,779 got a hypervascular arterial phase enhancing
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renal cell carcinoma, which is not a good
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prognostic sign, a poor prognostic sign.
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Some of the other poor prognostic signs include large
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size, tumor necrosis, which may affect the character
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of the diffusion, which I know you're going to discuss
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in a moment, um, obstruction of the renal vein or
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invasion of the renal vein with retroperitoneal
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collaterals, and transcapsular invasion.
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So we've got a diffusion image
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in the upper left-hand corner.
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Could you talk a little bit about if you
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would use diffusion, and if you would,
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how you would use it, and when does it restrict?
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So, diffusion weighted imaging is really
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what we're trying to master at this point.
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Uh, diffusion is really good in the
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two extremes, in cysts and in papillary
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cancers, because of the cellularity.
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When we're dealing with renal cell,
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we're dealing with low signal in diffusion
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weighted imaging,
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and we're dealing with low cellularity.
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So those two combined give us a very poor
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ability to use diffusion in our favor when
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we're dealing with clear cell renal cell.
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But when we're dealing with papillary,
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we will see restricted diffusion.
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The time when diffusion helps us is in
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talking about aggressiveness in renal cell cancers.
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So the more aggressive a lesion is, the more necrotic
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it is, then you will see more restricted diffusion
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in a lesion that you're strongly favoring to be
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a renal cell, a clear cell renal cell carcinoma.
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And
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I know this is confusing.
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It's even confusing for me.
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Um, but I know there's been recent reports
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that there is a correlation, there's a
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rough correlation between the ADC map
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and the restriction of velocity.
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So the lower the velocity, the
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higher the grade of the tumor.
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Unfortunately, you can see velocity restriction in an
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oncocytoma, in a chromophobe, and in an AML.
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So it's not specific for renal cell carcinoma, yet.
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The lower the velocity is on the
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ADC map, the nastier the tumor.
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That's correct.
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And then, but what they're looking
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at now is the intravoxel inherent
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motion, so the first part of the curve.
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And what they found is renal
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cells will have the higher spike.
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A chromophobe will have somewhere in the middle and a
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papillary would be at the lower end of the spectrum.
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And that's how we're trying to use
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diffusion weighted for histologic
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subtyping.
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And so, for those of you that are
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diffusion weighted imaging fans.
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You know, there are four major causes
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of diffusion restriction in the brain,
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but I just want to mention two of them.
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One of them is viscosity.
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And, of course, if you have a necrotic
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tumor, it kind of simulates an abscess.
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So a necrotic tumor or an abscess
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could produce diffusion restriction.
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And the other one that Dr.
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Fonazzo mentioned is cellularity or cell packing.
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So, you know, when you have really, really dense cell
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packing, say a lymphoma or a medulloblastoma of the
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brain, you're going to have diffusion restriction.
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So, as Dr.
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Finazzo mentioned earlier, in a renal cell you have
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very loosely packed cells, so you're not going
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to have cellularity-related diffusion restriction,
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but you could have viscosity-related diffusion
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restriction if you have a fair amount of necrosis.
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That's correct.
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Shall we move on?
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Sure.
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Dr. P and Dr. Finazzo out.
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