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Utilizing the Sequences

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Now let's look at our five-point scoring system,

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that we use for reading, but in truth,

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it's really a four-point system because nobody uses

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spectroscopy for reading, imaging, scoring.

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And in fact, many people, including our colleagues

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in Germany, don't even use dynamic contrast

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enhanced MRI for screening of the prostate.

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And have found no difference between

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the diagnostic study with DCE MRI,

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dynamic contrast-enhanced MRI,

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and the screening study that excludes it.

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So, if you are doing a screen, who might be a

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candidate for a screen that hasn't had a biopsy?

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Because that's a question that's often asked.

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The virgin prostate.

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Somebody with BPH.

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Maybe the prostate is gradually,

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slowly getting bigger.

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And the PSA is low, 4.5, certainly

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under 10, and it's rising very slowly.

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The patient isn't that symptomatic, otherwise.

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And the patient has no strong family history

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of carcinoma in the prostate, or in other

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organs like the colon and the pancreas.

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That would be a candidate.

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For somebody that has not had a biopsy,

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to have a screening MRI, looking for

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areas of diffusion restriction, especially

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in the peripheral zone, and morphologic

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abnormalities on the T2-weighted image.

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So, here is our T2-weighted image.

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Performed with the cardiac external coil.

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It is not endorectal, so there's been

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nothing placed in this patient's butt.

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The buttocks is collapsed because

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they've had the proper prep tuned into

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the vignette on prep if you need to.

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It's fast.

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It's inexpensive.

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The patients like it a lot better when you

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don't have to put anything in their rear end.

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So this is the way to do both

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screening and diagnostic MRI.

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Now I've got some of the

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parameters listed on the left.

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I'm not going to read them off to you.

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You can see the scan time.

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You can read them for yourselves.

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And this is an axial series of images.

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Look at the overall slice thickness.

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This is a

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3.5 millimeter slice thickness.

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So this is damage.

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2D technique, but exquisite detail showing

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you the peripheral prostate capsule.

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We'll talk about the anatomy separately.

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But I'm just showing it now

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for protocol assessment.

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And you would go up and down looking for what?

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Looking for areas of mass like, confluent,

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or round hypo intensity in the peripheral zone.

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What would you be looking for in

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the central zone on the prostate?

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The T2-weighted MR, something akin to wax on,

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wax off, something lentiform, something that

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looks like you took a piece of charcoal and

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started erasing the central and transitional

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zones whose anatomy will be defined shortly.

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So don't worry, we're on

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to anatomy in a little bit.

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Let's keep going on to the next

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portion of the examination.

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This is a T1-weighted image.

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This actually doesn't come

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into the scoring system.

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However, you'll have a

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T1-weighted image for a few reasons.

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One, it's awfully nice to look at the

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periprosthetic fat and see that it is clean.

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It's also an excellent way

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to depict bony metastases.

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It's also an excellent way to look

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for lymphadenopathy, the clean fat

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around the posterolateral corners.

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At 7 o'clock and 5 o'clock, with these small

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tiny little dots at 7 o'clock and 5 o'clock

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helps you clear the neurovascular bundle.

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So if you lose that circumferential fatty ring,

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then you have to worry, if you have a mass in the

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prostate, about neurovascular bundle invasion.

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So here is a coronal.

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Now, not every, not every scan

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needs to have a coronal projection.

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Uh, in fact, if you're doing the

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study three dimensionally, you can

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reconstruct the coronal projection.

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So this is an optional one to add to

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your screen, to your diagnostic study.

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You're probably gonna have a

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coronal for lesion localization.

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But not necessarily for the screen itself.

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And in the coronal projection parameters shown

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on the left, our abnormality on the T2,

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which looked a little rectangular, I'll go back to

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it for a minute, looks a little rectangular.

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It looks a lot more round in the coronal

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projection, and we're going to divide up the

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prostate into a base, a mid, and an apex,

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and that'll be a story for an anatomic day.

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But at the base, on the viewer's left,

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the patient's right, there is a round

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mass in the PZ, or peripheral zone of the

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prostate, where most of the cancers occur.

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Here's your hyperintense PZ, with a

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tumor growing straight out the top.

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So in this case, the coronal projection.

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Helps you localize the position of the tumor.

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Although, if you're pretty advanced,

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you wouldn't need to do that in the axial projection.

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You'd be, you'd figure it out by looking

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at the axials from top to bottom.

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And you would know where you are anatomically.

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If you want, you could also include a sagittal

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T2-weighted image for further localization.

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Although, for screening,

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that wouldn't be necessary.

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And again, if you have three-dimensional

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imaging, you can reconstruct your sagittal,

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you don't have to acquire it, and that gives

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you extreme efficiency in performing the exam.

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Then we've got diffusion-weighted imaging.

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This is the second most important, if not

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equally important, as part of the examination.

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So what we'll do is we'll get a

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baseline study, B0, in which the

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diffusion gradients are turned off.

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So it's basically a very, very fast,

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uh, Echo planar type, T2-weighted image.

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And then we start turning up the dial.

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We turn up the heat.

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That's what elevating the B value does.

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It makes the gradients tighter, higher.

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It shows with greater sensitivity

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diffusion restriction.

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And as we go from, say, 0 to 400 to 800 to

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1200 to 1600, an area that diffusion restricts

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gets brighter and brighter and brighter.

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As opposed to, say, an area that has high T2, like

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this one, gets darker as you dial up the B value.

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Now this is only a B700, but we like to go to

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a B value of at least 1400 and preferably 1600.

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What's the least B value that I will work with?

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154 00:06:56,590 --> 00:06:58,409 1200 works on most scanners.

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1400, very acceptable.

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1600, ideal.

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So this area right here, which didn't look like

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much of anything, oh, it's diffusion restricting.

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It has a lentiform or oval shape.

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These two stalwarts of the prostate MRI, the T2

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Spin Echo, Fast Spin Echo, 2D or 3D, and the diffusion

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weighted image are the guts of the prostate exam.

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You'll then take this information and you will

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convert it. As we'll see in a few moments, into

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a parametric map, a so-called a DC map, and the

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bright area that you saw in the left gland.

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Your right will now appear dark and we'll

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explain to you why that is in a moment.

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Another component of the MRI, less important than

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the ones you've already seen, less important than

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the T2, the diffusion, and the yet-to-be-shown.

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A DC map is the DCE-MRI.

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The Dynamic Contrast-Enhanced MRI.

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Its main value is in helping you further

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determine how aggressive a lesion is.

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If you see an area that immediately enhances

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in the first seven seconds after contrast

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administration, on the very first arrival of the

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contrast into the adjacent vessels nearby, odds

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are you've got at least eight, nine, or ten.

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And especially if this intensity starts to smear.

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Like cream cheese on a bagel, that means

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that it's washing out, and that's another

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negative, ominous sign that you're

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dealing with a Gleason 8, 9, or 10.

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Other signs that you're dealing with a high

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grade Gleason lesion are size, bulkiness, extreme

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diffusion restriction, very low signal on the

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ADC map, broad areas of abutment of the capsule.

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All signs of something that is more aggressive.

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So here we've got a combination of the dynamic

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contrast-enhanced MRI in a different patient

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and a T2-weighted image in a different patient.

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This is cancer, this is an aggressive cancer.

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So we're showing you two aspects of the exam.

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Now here is something else that you

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can do as an option and that is the

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three-dimensional T1-weighted image.

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I don't routinely perform this,

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but if you're looking for very small nodes, or you

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really want to drill into the neurovascular

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bundle and you're not sure if you see the bundle

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around the edges at 5 and 7 o'clock around the

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prostate, you may opt for one-millimeter axial

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slices using some form of T1 appearing GRE.

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I don't do this routinely.

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You can also reformat or reconstruct it.

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Now let me show you the ADC map, which is the

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second most important part of the examination,

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or perhaps even the most important part, and it's

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derived from the diffusion-weighted sequences.

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So diffusion and ADC map,

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for you beginners, go hand in hand.

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Diffusion makes the map.

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So what is the map?

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The map is a pixel-by-pixel blow, in other words,

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a blow-by-blow, a blow-by-blow description,

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that's hard to say, of the velocity of flow blow.

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In each single pixel on the image.

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So if you have diffusion

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restriction, what's the velocity?

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Lower, right?

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Because it's not moving.

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It's restricted.

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So the lower the velocity,

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the lower the intensity on the ADC map.

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So what's bright on diffusion?

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Dark on the map.

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So that's how you do it.

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So you've got a mass on the

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T2 weighted image in the peripheral zone.

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You've got diffusion restriction

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that's bright on the diffusion image.

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You've got low signal intensity

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on the parametric ADC map.

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And if you choose to do dynamic

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contrast-enhanced MRI, and the lesion

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is aggressive, it will enhance early.

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And therefore be bright on this color

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flow map of dynamic contrast-enhanced MRI.

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So that's the exam.

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Notice I did not show you a spectroscopy.

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I also said that the DCE MRI does not have

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to be performed in every single individual.

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It's going to be elective and selected

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by you based on judgment and the

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scenario, but you must have the T2, the

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diffusion, and the ADC parametric map.

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