Interactive Transcript
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So this is another patient with biopsy-proven
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rectal cancer and comes to us for staging purposes.
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So in this instance, um, you know, there are two
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or three findings on the MR that are critical to
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make and also in terms of take-home messages.
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Uh, there are two sort of key take-home messages here.
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So the first thing that is obvious is, you
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know, when you look at this tumor, the bulk
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of the tumor has a very bright T2 signal.
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When you have a lesion or a rectal cancer
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that demonstrates high signal intensity and
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by high, I mean similar signal intensity to
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that of fluid in greater than 50 percent of
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the tumor, we call those tumors mucinous.
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Subtypes.
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Why is it important to make that
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morphologic distinction and why is it
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important to call attention to that?
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It's important because these mucinous
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tumors typically, they are bad actors.
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They typically, when they present, are more
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advanced in their, uh, local staging, uh, they
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have a higher propensity to cause nodal mets
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and they have a higher propensity to spread.
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And so typically these patients have worse
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prognosis than those that do not have the
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mucinous, uh, subtype of the adenocarcinoma.
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And so, uh, this particular cancer, as you can
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see, you know, the bulk of the tumor is T2 bright
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signal, so clearly is, uh, is a mucinous subtype.
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The second interesting part here is that the lesion is
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in the inferior aspect of the lesion is in the lower rectum
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because, as you know, this is only four centimeters.
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So clearly it is involving the mid to low rectum.
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And so here is one example where
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you have a tumor low-lying.
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And when you have a low rectal cancer, you have
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to tweak the template in terms of reporting.
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And so let's look at this, uh, tumor in
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the different planes so that, there you go.
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So as I'm scrolling on the sagittal, you can
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clearly see that there is a large tumor that
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is going well beyond the, um, lumen into
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the surrounding fat and it's very bright
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and more than 50 bright in signal intensity.
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So this is mucinous. It's low-lying.
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Now these patients typically, as I said, they are
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advanced in terms of rectal staging.
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Now if you pay close attention on the true axial
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you can see that there is a lymph node right here
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posteriorly, which is sitting right on the mesorectal
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fascia, and this node is bright in signal intensity.
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So remember, as I mentioned earlier, when you
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have a positive node that contains mucin in
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a patient who has a primary mucinous cancer,
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you do not use any of the size criteria.
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You just call this node positive because
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it clearly has mucin within it, which
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reflects what you see in the primary tumor.
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So this is a positive lymph node.
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The patient does have additional nodes that are not
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mucin-containing.
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There is also an obturator node right
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here, which is not mucin-containing.
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And in those instances, you will follow
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the same criteria that we talked about.
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So in this case, so this is
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between 5 and 8 millimeters.
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You have to look at any two.
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So is it rounded?
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It looks sort of rounded.
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It has ill-defined margins, has no heterogeneous
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signals, so it meets two of the criteria.
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So that clearly means that it would be a positive
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node and the obturator node that we see right here.
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So remember, the reason it's obturator
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is because if you draw the line like
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so it's not medial, it's lateral to it.
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So that's along the obturator antenna.
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So this is an obturator node.
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And if I okay.
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Again, measure the short axis.
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Remember, for the pelvic side, well,
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it has to be more than 7 millimeters.
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This does not meet the criteria.
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And so that's, um, it's not positive.
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So again, you can see the outline of
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the mesorectal fascia and clearly here,
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posteriorly the tumor is reaching it.
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So the MRF is involved in this case, has
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positive nodes and it has mucinous pathology.
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Now the other thing is, when you're looking at
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the lower extent of
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the cancer, in terms of lower rectal cancer.
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So remember when we talked about anatomy, I told
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you the mesorectal fascia, as you come down into the
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pelvis, it is closely approximated to the rectal lumen.
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And in the pelvis, the mesorectal fascia basically
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inserts on the puborectalis and on the levator muscle.
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So, when you are talking about low rectal cancers in
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your template, in terms of looking at MRF extent, you
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measure the shortest distance to the levator muscle.
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Rather than, you know, looking at mesorectal
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fascia because you really cannot identify the
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mesorectal fascia lower down in this region.
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So when in this particular instance, you
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can see on the coronal, I can see the
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iliopsoas muscle on the right side.
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And as I'm scrolling through, and here it is on the
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right side, on the left side, it clearly is involved.
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So the iliopsoas muscle is involved and there is perhaps
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a bright signal extending, as you can see right here,
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beyond the iliopsoas or the part of the levator ani.
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And so when you have levator muscle involvement, in this
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instance, it indicates that this is T4 disease.
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So the two take-home points in this
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case are if you have more than 50%
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involvement of the tumor with T2 bright signal.
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It's a mucinous subtype of adenocarcinoma,
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and you have to call attention to that in
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your report in terms of morphologic evaluation
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because these tumors typically are bad actors.
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They have worse prognosis and they
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are higher in grade and staging.
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And if there is accompanying adenopathy,
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which is bright in a T2 signal, you do not
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use the conventional size criteria for adenocarcinoma.
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Instead, you call that node positive.
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If you have a tumor that is in the lower
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rectum, in that instance, for the status of
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the mesorectal fascia, there is no shortest
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distance to measure because the mesorectal
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fascia is closely applied to the levator ani muscle.
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So for low rectal cancer, the take-home
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message is to give the shortest distance to the
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levator ani or the shortest distance to the
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puborectalis, depending on where the cancer is.
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Because if there is involvement of the levator
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ani, as is the case in this particular
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patient, that indicates it's T4 disease.
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