Interactive Transcript
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Dr. P here back with our 72-year-old woman with a known
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3 00:00:04,860 --> 00:00:07,790 greater than 4 centimeter anterior inferior pole left
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renal mass. I'm starting out with two quick images
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from our in-phase out-of-phase Dixon method M Dixon
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method and fat sep series: the fat-only image and the
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water image as part of that subtraction. The fat-only
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image has lots of fat inside, nice and bright, whereas
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the water image shows the lesion to be very dark,
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dropping out, virtually having no signal intensity,
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and the lesion therefore contains macroscopic fat.
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The lesion is consistent with probably one of the
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most commonly encountered benign solid renal tumors,
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known as angiomyolipoma, which occurs in adult women.
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They're now classified as part of the family of
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perivascular epithelioid cell tumors, or PEComas.
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Now AMLs are typically composed of blood
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vessels, so they're vascular, smooth muscle
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components, and mature adipose tissue.
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Most of these are sporadic, but occasionally
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you'll see them in association
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with tuberous sclerosis complex.
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An example of AML associated with tuberous sclerosis
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complex is the epithelioid, a rare type that contains
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few or no fat cells, the epithelioid type of AML.
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Epithelioid AMLs may demonstrate aggressive
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clinical behavior, including extension into
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the inferior vena cava and even metastases.
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So a different behavior for the
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tuberous sclerosis complex type of AML.
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Now in 10 percent of cases where AMLs are really big,
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greater than 4 cm, and that's why I measure the 4 cm
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size, there's an increased risk for potentially life
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threatening hemorrhage known as Wunderlich's syndrome.
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It's also found that tumors that have ruptured
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have sometimes large pseudoaneurysms greater
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than 5 mm in size, suggesting those seen in
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angiography are hemorrhagic pseudoaneurysms.
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Now, rarely, large AMLs can be considerably exophytic
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and difficult to differentiate from perinephric
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liposarcomas, but fortunately, again, that's very rare.
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Features that help suggest an exophytic AML include
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a well-marginated lesion, which our lesion is.
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It's extremely well-marginated.
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A sharp renal parenchymal defect
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with a sharp renal interface.
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We have that here.
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And the presence of enlarged vessels, which you
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may see on a CT angiogram or on a real angiogram.
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Now let's continue looking at our lesion and
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see some of the other characteristics of it.
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Here's a simple T2 without fat suppression.
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And yes, these lesions have a vascular component.
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So, we didn't fat suppress this, so it doesn't
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dissuade me from the diagnosis, the very fact that it
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is somewhat hyperintense on the T2-weighted image.
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Let's look at the diffusion MRI.
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On diffusion MRI, there's no diffusion
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restriction, which you might see with a
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solid, cellular, heavily packed lesion.
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And as you know, there are several causes of diffusion restriction:
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one of which is viscosity, another which is
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cell death, another which is cell packing.
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So this lesion does not demonstrate diffusion
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restriction implicating those underlying etiologies.
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So we're into this diagnosis of
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angiomyolipoma, and we're going to continue
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on discussing it in the next vignette.
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