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Case Review: PI-RADS 5 With Capsular Involvement

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Let's take this 66-year-old man with a PSA of 6.55,

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positive physical examination, and

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utilize this to drive home three points.

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PI-RADS grading, T staging,

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and capsular involvement.

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So let's start with PI-RADS grading.

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This is a basic PI-RADS

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grading case of a PI-RADS 5.

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There is a mass, some portions of it nodular,

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some ill-defined, infiltrating the entire left

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portion of the gland without crossing the midline.

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The mass, as we'll see in a moment, meets

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major peripheral zone criteria, which is

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diffusion restriction, heavy diffusion

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restriction, at the locus of the mass.

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The T2 criteria are more important in the TZ

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central region, the diffusion criteria more

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important in the PZ peripheral region.

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The fact that the mass is greater than 1.5

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centimeters in size makes it a PI-RADS 5.

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1.5 and under would make it a PI-RADS 4.

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5 and under would make it a PI-RADS 4.

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Now let's take issue number two, the T stage.

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The T stage reflects the

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size, extent, and magnitude.

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Non-local, as well as local extent of the mass.

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So, do we have a mass that

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extends out of the prostate?

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That's probably one of the most

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important T stage criteria.

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So, what would be a T2?

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A T2 would be a tumor involving

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one half of one lobe or less.

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A T2B would be a tumor involving more than

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one half of one lobe, but not both sides.

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A T2C would be involvement of both sides.

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A T3 would be involvement of the prostate capsule.

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And a T3B would be involvement

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of the seminal vesicle.

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So let's take a look at our seminal vesicles.

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We saw in a companion case that we had

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a desiccated seminal vesicle on the

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left and an invaded one on the right.

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Here we've got normal seminal vesicles.

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With a typical glandular secretory acinar pattern.

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And in fact, we see some proteinaceous

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material that is layering dependently.

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These are normal seminal vesicle glands.

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There is no seminal vesicle involvement.

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What about T3A?

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Is there capsular involvement?

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And the answer is yes.

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There is likely capsular involvement.

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And what do we use to make that determination?

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That there is capsular contact

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for at least two centimeters.

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Not only is there capsular contact for at

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least two centimeters, but if we blow up

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our coronal projection, and this is why

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we look in every projection, we've got

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capsule, anatomic capsule, anatomic capsule

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violated, transgressed by this tissue.

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Not quite as easy to see in the

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sagittal projection, but suggestive.

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So, you should suggest that there is capsular

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invasion, that this is a T3B abnormality.

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Now what about regional nodes?

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If regional nodes are not

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assessed, then we say NX.

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If regional nodes are positive, then

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we'd say that there is an N1 abnormality.

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And that's a pathologic designation, but if

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we are confident that we have regional nodal

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involvement on MRI, we'd say MR suggestive of N1.

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A T3a N1 abnormality if nodes were present.

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If nodes are not present, then we'd say N0 by MRI.

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So you have NX, not assessed.

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N0, not involved.

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N1, regional nodes involved.

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What about distant metastases?

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Distant metastases, M0, no distant mets.

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M1, M1A, non-regional lymph nodes,

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M1B, bony metastases, and M1C, other

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sites with or without bone involvement.

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In this case, we did not have evidence

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of distant metastases, so we would have

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an M0, at least by MRI, not by pathology.

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Now, let's turn our attention to the

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major criteria for the peripheral zone,

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which is the diffusion image, and see if

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there is high signal intensity diffusion

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restriction on the high B-value image.

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And indeed, there is, in the

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left portion of the gland.

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And it's highly diffusion restricted.

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It's very hyperintense, meaning it's

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likely to be a Gleason 9, 8, or 7,

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above a Gleason 6.

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Let's put up the corresponding ADC map.

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There should be low velocity pixel by pixel

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illustrated by darker signal intensity

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in the left hemigland and there is.

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You can actually calculate these values and

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the lower the velocity, the higher the Gleason

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stage or Gleason histology is likely to be.

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For our final act, let's

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put up a B0 diffusion image.

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The tumor is darker than the normal gland.

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Now let's put up an intermediate B-value image.

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The normal gland, still a little bright.

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The tumor, still a little gray.

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Let's take a higher B-value, say around 1200.

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Now the tumor getting brighter,

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the gland getting darker.

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And then the B1600 value, the tumor is

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brighter and the normal gland is darker.

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So they invert.

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When you're at a B-value of 0, in

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other words a T2 image with echoplanar

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technique, the tumor is solid and gray,

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the normal peripheral zone is bright.

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But as the B-value goes up, the tumor gets

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brighter, the normal gland gets darker.

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The brighter that gets, the

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worse it is for the patient.

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And the more likely the patient is to have

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a histologic advanced Gleason stage.

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So we've illustrated three key points.

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An obvious left hemigland

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not crossing the midline.

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PI-RADS 5 lesion measured

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length, width, and height.

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I'm not going to measure it for you right now.

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A suggestion on MRI of transcapsular extension.

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We've illustrated the technique for T, T

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stage grading, including nodes and metastases.

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We stuck with the higher T-stage grades.

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And then finally we gave you some

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subtle and not so subtle criteria

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for assessing capsular invasion.

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Two centimeters of capsular

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contact, bulging, bulging, bulging.

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One I didn't describe, the facement

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of the neurovascular bundle.

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And then finally, directly seeing the anatomic

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capsule, as we did in this case, transgressed.

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This was also a hypervascular tumor on DCE MRI.

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PI-RADS 5.

Report

Faculty

Stephen J Pomeranz, MD

Chief Medical Officer, ProScan Imaging. Founder, MRI Online

ProScan Imaging

Tags

Prostate/seminal vesicles

Neoplastic

MRI

Genitourinary (GU)

Body