Interactive Transcript
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Dr. P back with our 72-year-old woman with a
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3 00:00:03,390 --> 00:00:05,790 greater than four centimeter mass known now to
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us as an angiomyolipoma. Angiomyolipomas can be
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classified as classic with macroscopic fat and
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what we call lipid-poor AMLs depending upon
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their appearance. I put up before you an axial T2
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non-fat suppressed and one that's pretty, pretty
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heavily fat suppressed. Now on the standard T2
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Uh, the lesion is somewhat hyperintense, but not
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that much greater in signal than the surrounding
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fat, but certainly hyperintense to the kidney.
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On the fat-suppressed image, a large
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component of the lesion is dark and fat
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suppressing, but some components are white.
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So you're probably asking, well, what's
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the signal intensity on T2 imaging?
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And the answer is, it depends.
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Depends on the vascularity, how much smooth muscle.
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Do you have pseudoaneurysm formation, and how much fat?
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So, you can't really use the T2-weighted
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image as what I call the DECIDA scan.
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You've got to go through everything, especially
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looking at something that is very sensitive for
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fat, like fat suppression imaging, or Dixon method
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imaging, or in-phase or out-of-phase, uh, imaging.
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These lesions, as we said
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previously, are hypervascular.
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Now, classic AMLs are easier to diagnose than these.
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Because they have the typical pathologic
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hallmark of macroscopic fat, seen
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on even a basic T1-weighted image.
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And they're readily identified
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on cross-sectional imaging.
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But the lipid-poor ones, you know, that may be a
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challenge to differentiate from renal cell carcinoma.
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This is a pretty exophytic,
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uh, looking lesion right here.
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And that's a critical diagnosis.
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In my experience, most renal cell carcinomas
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don't have this very exophytic irregular appearance.
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They may be exophytic, but they tend to
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have more of a smoother, rounder appearance.
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But in ambiguous cases, you're going to have
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to use a number of factors, diffusion imaging,
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the parametric factors when you inject the case
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to see how much vascularity there is in there.
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Both can be very vascular, and how much
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washout you may experience thereafter, and
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sometimes it can be extremely difficult.
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I have seen kidneys completely resected
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from Wunderlich Syndrome with a massive,
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massive hemorrhage from an AML, and it's not
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until you get the specimen on the table that
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you realize you just took out a benign lesion.
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Now, the presence of macroscopic fat can be
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appreciated as suppression of signal intensity
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on these fat suppression images, as you've seen.
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Especially on the India ink
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artifact scan, the out-of-phase.
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So if you can't do Dixon method, just
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do in-phase imaging and out-of-phase
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imaging, as you've seen previously.
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Now, benign lesions, as we've said before,
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including classic AMLs, may be exophytic.
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But this angular interface, and you do have
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a little bit of a claw sign here, admittedly.
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But this sort of angular, irregular appearance
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supports the diagnosis of angiomyolipoma,
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and I'm scrolling through it on the
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T2 and the T2 fat suppression imaging.
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But in some studies, such as the study by
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Takayashi, Takayashi and others, the angular
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interface sign is present really uncommonly,
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less than 10 to 20 percent of the time.
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So that alone isn't going to get you off the hook.
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You'll also hear the sign, the mushroom sign, where
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the lesion appears to mushroom right out of the kidney,
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which it's doing right here on the T2-weighted imaging.
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So there are a number of things you can use.
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The mushroom sign is one of them.
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Hypervascularity.
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Relative lack of washout.
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The absence of diffusion restriction.
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The presence of macroscopic fat.
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Perhaps the angular interface sign, the demographics,
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usually an adult or slightly older woman.
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All of these things combined might help you
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towards the diagnosis of the benign angiomyolipoma
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and away from renal cell carcinoma, which
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can also have micro and macroscopic fat.
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Dr. P out.
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