Interactive Transcript
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60-year-old man with an elevated PSA to 5
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without family history or obstructive symptoms.
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For images, we have an axial T2-weighted image.
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We have the axial ADC map, which is windowed
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and leveled at 1400 and 1400, respectively.
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We have an interpolated B equals
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1600 diffusion-weighted image.
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That's our high B value image.
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And we have the arterial phase images
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from a dynamic post-contrast series.
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All right.
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So, The first thing you notice is that
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the transition zone is very large.
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It's compressing the peripheral zone, but
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we look at the peripheral zone anyway.
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On the ADC map, it's very nice, high T2 signal
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throughout, so there are no focal areas of well
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defined diffusion restriction in the peripheral zone.
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And the peripheral zone, Focal diffusion
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restriction is the finding that we use to
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direct us most often to a suspicious lesion
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that's going to be Pirads 4 or Pirads 5.
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The transition zone, uh, is evaluated
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mostly on the T2 images, with diffusion
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and post-contrast having secondary roles.
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The Transition zone is very large.
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It's got a very heterogeneous appearance.
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This is sort of your typical appearance of nodular BPH.
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You have areas of high signal, low signal.
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You have nodules that are very well-defined, right?
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And inside the nodules the
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appearance can be very heterogeneous.
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The finding in the transition zone that
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jumps out at me is this region right here.
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It's about 1.
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5 centimeters in diameter.
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It's well-defined, low T2 signal.
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here and maybe causing some mass effect using the
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Pirads lexicon. Want to know is it circumscribed
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or non-circumscribed and what that means is are the
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margins well-defined or non-well-defined, right?
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Encapsulated is another term in the Pirads lexicon. An
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encapsulated nodule will actually have a well-defined
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low signal rim around it like here and here and here.
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So we're looking at are the margins
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distinct or not distinct. Okay, are we?
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Circumscribed or non-circumscribed.
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So if you look on the axial images, when
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we read this initially, we thought that the
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nodule was non-circumscribed, that its margins
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were not very distinct, and if that's the
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case, this gets called a Pirads 4 lesion.
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Now if you look on the sagittal images, you
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might convince yourself that the margins
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are very distinct, in which case it's not.
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This would be called a Pirads 2.
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So this leads, so this, this leads to some issues.
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And if you can't decide if it's a 2
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or a 4, you can always call it a 3.
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Sometimes you can look at your
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diffusion images to help, um, characterize.
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Because in the transition zone, right, if
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you have a score of 2 based on the T2, but
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you have a score of four for diffusion,
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you can bump the score up to a three.
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And likewise, if you score a three for the T
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two appearance and you have a high diffusion
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score, uh, then you can bump it up to a four.
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Right?
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If the DWI score is five, and since the
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diameter of this is about 1.5 centimeters, if we
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thought it really, truly restricted diffusion,
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it would get a score of five for diffusion,
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and this would become a Pirads 4 lesion.
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Right.
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I know it seems very complicated.
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So in this case, uh, the area has well
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defined diffusion restriction on the ADC
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map, but it doesn't have well-defined focal
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diffusion restriction on the high B-value image.
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So this gets a diffusion score of 3,
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which means we're not bumping up the
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total Pirads score based on the diffusion.
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So that's unfortunate.
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Interpreted this, we had two thought processes.
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One was, um, it may be doesn't have
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distinct margins, and we're going to call it
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a Pirads 4, and we're going to biopsy it.
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The other thought process was, this is the only
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thing in the transition zone that looks like this.
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BPH appearance, but this nodule is solid,
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it's clearly not within an existing nodule,
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it's causing some mass effect on a nodule,
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and it may have diffusion restriction.
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Um, it did not contrast-enhance, all right, which
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didn't factor into our decision very much at all,
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to be honest with you, because um, a lot of things
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enhance or don't enhance in the transition zone.
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This was biopsied and came back as normal tissue.
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Now, this is actually a good case to talk about
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how difficult these studies can be because if
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you look at this patient's PSA density, it's 0.05.
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Alright, so in our practice, uh, we
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only, um, biopsy PI-RADS 3 lesions in
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patients whose PSA density is less than 0.15.
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Uh, and we do that mostly to limit the number of
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biopsies in those patients, so we'll get followed
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up very closely, and the biopsy is pretty invasive.
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Uh, so in this case, if we had decided to call this
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a PI-RADS 3 or 2 instead of a 4, the patient might
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not have gone to biopsy and biopsies aren't the
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most pleasant experience and being a large gland
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and an anterior lesion, this could have been very
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difficult to biopsy and perhaps in retrospect it was.
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So this is probably not the best case to to
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show as the first case in the fellowship, but
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it is a good case to to show how complicated
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sometimes these transition lesions can be.
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In many subsequent cases, we'll see some very
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straightforward peripheral zone lesions, we'll see
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some very straightforward transition zone lesions,
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and we'll see a couple that are difficult like this.
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And the thing to remember is, right, just
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because there are a couple, Um, a small
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number of very, very difficult cases really
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doesn't invalidate the entire technique.
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A lot of sites, including ours, have had
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very great success at limiting the number
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of men requiring an unnecessary biopsy by
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using MRI and using the PI-RADS criteria.
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And we found that when we do this consistently and
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do this well, a very large percentage of the men that
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we biopsy end up having, uh, significant cancer.
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And that really lowers the risk of having a PSA
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test, which is, you may go on to a biopsy you
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don't need, or you may incompletely characterize
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a lesion and end up overtreating low-risk
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lesions and undertreating high-risk lesions.
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So apologies for starting the fellowship
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with a difficult case, uh, but hopefully
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it will be a lot easier from here on out.
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