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Case Review: Staging a PI-RADS 5 Lesion

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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.

Report

Editorial Note

Faculty

Stephen J Pomeranz, MD

Chief Medical Officer, ProScan Imaging. Founder, MRI Online

ProScan Imaging

John F. Feller, MD

Chief Medical Officer, HALO Diagnostics. Medical Director & Founder, Desert Medical Imaging. Chief of Radiology, American Medical Center, Shanghai, China.

HALO Diagnostics

Tags

Prostate/seminal vesicles

Neoplastic

MRI

Genitourinary (GU)

Body

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