Interactive Transcript
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Let's take this 66-year-old man with PSA
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of 12.27, prior negative biopsy,
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and no history of carcinoma.
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He has had a physical examination that is
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positive for a nodule and is symptomatic.
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We have an axial T2 fast spin echo
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image, and the purpose of this case is
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to introduce you to the basic analysis
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of a high-grade cancer and a stager.
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So staging is key.
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And we're going to stage
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according to the T-stage system.
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So we're going to have a T-stage,
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an N-stage, and an M-stage.
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So let's begin with our cancer, which is
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solid, intermediate in signal intensity, and
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has transgressed key anatomic boundaries.
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It has violated the surgical capsule.
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The surgical capsule is really a
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pseudocapsule between the central
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TZ gland and the peripheral gland.
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Here it's intact.
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Here it's violated.
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The cancer has violated the anatomic capsule.
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There's the intact left anatomic capsule.
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There is the transgressed anatomic capsule.
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Let's scroll it.
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Let's go up and down.
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And this lesion has gone all the way
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from the apex, low in the prostate,
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to the base, high in the prostate.
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In fact, it's gone into the base and
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involved the right seminal vesicle.
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Now as one ages, the seminal vesicle, which
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is normally hyperintense, becomes more hypointense
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due to desiccation of secretions and
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sometimes the simple mere fact of obstruction
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can produce desiccation of the seminal vesicle.
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But we still see its glandular
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acinar appearance or architecture.
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On the right side that architecture is lost.
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continuous with the rest of the mass.
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Now let's look at the dynamic contrast
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enhanced MRI, which is purely a supplement.
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Because any DCE MRI can still
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qualify you for a PI-RADS 4 or 5.
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This one happens to be a hypervascular
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lesion, which is a poor prognostic sign.
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And let's get right into the center of the tumor.
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So here's the center of the tumor.
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And let's go to a mask.
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And now let's follow the contrast.
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Contrast has not arrived yet.
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Contrast has arrived.
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The right gland
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is brighter than the left gland.
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So if we look at the curve of the normal
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gland, it would look something like this:
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Pretty quick arrival, and then as time
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goes on, we'll see it keeps going up.
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Whereas the right gland, the tumor enhancement
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on DCE MRI, is going to look something like this:
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It's going to rise very quickly, as it does right
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here, and then as we follow it, it's going to
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come down and eventually they'll meet so that
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as you get deeper into the time activity curve,
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they're going to become equal in enhancement.
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So let's do that.
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Let's keep following them.
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Let's take away our curves.
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This is getting less bright.
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This is getting more bright.
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This is getting less bright.
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That's getting more bright. This is getting
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less, that's getting more, and they are equal.
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That is typical of a tumor curve on the
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right and a non-tumor curve on the left.
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Now let's go to our diffusion portion of the exam.
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We've got a diffusion image in the lower right
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hand corner showing the scope of the cancer.
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And very hyperintense.
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If we go to an earlier image with a
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B value of 0 or 500 or 700 or 800, this
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area is not going to be as bright.
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But as the B value goes up, this gets brighter.
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I'm going to illustrate that for you in a second.
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Interestingly, this portion of the tumor, the
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brightest portion of the diffusion restriction
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in the anteroapical region, was a Gleason 9.
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This portion, brighter near the
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base and the back, Gleason 9.
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The rest of it, Gleason 7.
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This is proven on TRUS, on transrectal
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ultrasound biopsy imaging with MR as a map.
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The ADC parametric map, which is
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a map of velocities, shows the
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restricted velocity of the main tumor.
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The greater the degree of restriction we
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know correlates with the Gleason grade.
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So the lower the velocity, the darker
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the signal, the higher the grade.
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And that correlates very nicely with
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what we saw on diffusion imaging as well.
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So this area back here that's a
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little bit blacker, Gleason 9.
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These areas that are a
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little bit grayer, Gleason 7.
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And the apical region that we
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saw correlated with a Gleason 9.
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Now, let's look at some of the other projections.
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So let's take a look at the
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coronal projection for a moment.
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I'm just going to drop it in the left-hand corner
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and keep my diffusion image up, because I promised
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to show you the individual diffusion images.
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And we have our best look at seminal
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vesicle invasion on the right.
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We have involvement of the base, the
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mid, the apical, the lateral, and
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mesial segments of the prostate gland.
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If we were to localize this tumor axially, we'd
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say that its epicenter is in PZP and PZM, with
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extension into TZA and TZP from apex to base.
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We'd say that the capsule is transgressed,
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both laterally and posteriorly, and we'd
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say that it's transgressed laterally.
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With crossing of the right-sided
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Denonvillier rectoprostatic fascia.
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We would say, in the sagittal projection,
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that the mass does not invade the preprostatic
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space of Retzius, even though the Gleason 9
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component was, in part, antero and apical.
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We would say that the bladder base is not invaded.
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We would say that the pelvic sidewall
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in the coronal and axial, not shown right
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now, is also not affixed by the mass.
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Now let's return to our diffusion sequences.
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So let me start with this one.
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This would be a b value of zero.
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Let's go to an intermediate b value.
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Let's go to a higher b value.
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And then let's go to the highest b value.
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Now the things that cause diffusion
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restriction, and you've heard this on multiple
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vignettes, are viscosity, cellularity,
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cell membrane interruption, and so on.
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Cell death, cell necrosis.
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The ones that apply here in prostate
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cancer are desmoplasia, or firmness of the
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lesion, and cellularity, or cell packing.
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That can also occur, by the way, in the
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bone marrow, as we'll see in a moment.
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So now let's scroll.
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Let's focus on our tumor.
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I'm gonna make it a little bit bigger.
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Let's focus on our tumor.
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Keep focusing while I'm making it
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bigger, and look what's happening.
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Our tumor, as the B value goes
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up, is getting a little brighter.
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A lot brighter.
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Brightest, as we go from B value
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to 0, to 800, to 1,200, to 1,600.
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And the areas with the highest signal
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intensity have the highest Gleason scores.
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But wait, there's more.
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There's involvement of the pubis.
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There was involvement of
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other skeletal areas, too.
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And just as you would with PET CT, you're
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going to take each of these dots, and
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correlate it with a morphologic image.
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So you might pick up, say, the axial T2, for
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instance, and then you would look to see if
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those dots correspond to linear tubular vessels,
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or whether they correspond to lymph nodes.
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So in this particular example, the
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patient did have positive lymph nodes.
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There are a few of them that are, like this one,
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very tiny, micrometastases, non-tubular, there it
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is right there, and
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It's there, it's there, it's gone.
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There, there, gone.
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So not a tube.
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Whereas some of these are very
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squiggly and wiggly like that.
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That's obviously a vessel.
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You don't even need the
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anatomic image to prove that.
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But you go back and forth like you would
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with PET CT to decide what's anode, what's
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round, what's gray, what's lost its fatty
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hilum, and what is a tubular structure.
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So in staging this lesion,
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we've got a T three B lesion.
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We've also got nodal metastases, so it'd be an
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N1 for nodal metastases as opposed to an N zero.
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And we've got an A, a metastatic lesion in the
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bone, which would make it an M1 B for bone lesion.
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So T three BN one regional nodes, M1 B for bone.
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There's seminal vesicle invasion,
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there's transcapsular extension.
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We give the tumor volume.
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We'd say the right
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neurovascular bundle is invaded.
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The right rectoprostatic fascia is invaded.
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The lesion is not affixed to the pelvic sidewall.
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There's bony metastases.
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And there are regional nodes.
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By the way, don't forget to
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look at the rest of the scan.
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Yes, you looked at the bones, but there
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is an ileosois bursal cyst on the right.
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And there are some other
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additional minor findings.
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That is an example of a PI-RADS 5
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with T staging illustrated.
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