Interactive Transcript
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Dr. Schupack,
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we've got a 28-year-old male with visual loss,
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probably a visual field cut,
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a sagittal T1 with contrast,
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some moderate but definite enhancement of our mass.
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Here's the pre-contrast.
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T one. Here's the post.
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And here's the axial.
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T two spin echo. So again,
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in approaching a lesion of this size,
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we want to know the gender,
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we want to know the age which we have.
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We want to see if the lesion is smooth and or solid,
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which it is. Are there any cysts?
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No. Is there calcium? No.
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Is there blood? No. Is there fat?
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Answer is no. Then we say to ourselves, okay,
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is it intraaxial? For instance,
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is it arising from the hypothalamus?
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No. Is it arising extra axially?
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Probably from the Pituitary gland, can't separate it out.
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And then if it's intracellular,
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what kind of other characteristics does it have?
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And we've already alluded to those.
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If it's supercellular, is it a general mass in an adult?
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Or is it a pediatric patient?
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If it's a pediatric patient,
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then our differential diagnosis changes.
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And then what's the status of the stalk in this case?
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The stalk is compressed.
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It clearly is not arising from the stalk.
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It's not a primary stalk lesion like a
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met or e g or sarcoid or pituocytoma.
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And then we go back to the clinical question,
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which is the patient has a visual field problem where's
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the optic apparatus, it is markedly compressed.
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So this lesion is going to be dealt with.
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And then as I look at it and decide it's infrastellar
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extension, I'm also thinking,
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is there retrocellular extension? Yes, there is.
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You can talk about that in a moment.
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Is there anterior extension? Not much.
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Is there infrastellar extension? There certainly is.
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And is there paracellar extension?
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There certainly is. To the left.
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So I'll drive, and you can address some of those issues.
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Okay, well, in the earlier vignette, dr.
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Pomez gave a very detailed differential.
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Of cellar supercellar masses.
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And he loves to do stuff like that.
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I do.
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But I would say the first thing is if you look
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at ones that really enlarge the cella,
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that list gets a lot smaller.
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True. Meaning something like sarcoid, epidermoid,
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some of these things are just not going to do this.
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So when you talk about things that are definitely
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eroding and enlarging the cella,
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you've already cut down that list
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and this one is doing that.
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I'm going to inject one thing radiographically
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and that's so right, as usual.
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But look what it's doing to the clivus, right?
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It's not destroying the clivus, it's remodeling.
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It's almost like somebody just went and cut the clivus
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off right there. You can still see a cortical rim,
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so that tells you it is not a malignant aggressive lesion,
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right? Remodeling, remodeling. Now,
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so some something like this.
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Okay,
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so let's just say that we're talking about a primary
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cellar lesion. Let's say we decided that there's.
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Cyst. The clivus doesn't look right.
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Okay,
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so maybe adenoma, macroadenoma. Now, I'll tell you,
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when I see something
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aggressive like this taking out the skull base,
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I think of prolactinoma, okay?
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Those are very aggressive.
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I remember very clearly somebody coming in when I was at
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the Mayo Clinic and I had to put the patient into
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a halo emergently because a lesion like this,
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I've basically taken out their skull base condyles.
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Okay?
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So when I think of an aggressive lesion so we talked
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before. Before you get into some major commando thing,
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let's be sure to check the prolactin
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and see what's going on here.
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So I think that's the first thing is does
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look like a macroadenoma. It'll do it.
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But make sure you check that prolactin because
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prolactinomas are evasive and that's the
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kind of stuff they'll do, and they can.
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Pretty nasty resect,
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which I know you'll talk about in a minute.
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But I want to clarify one thing.
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I said the lesion was behaving radiographically in
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a non-aggressive way relative to the skeleton.
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What I meant by that was it wasn't malignant.
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It wasn't wiping out the bone.
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But you're so right.
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It does have an aggressive growth pattern or behavior
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other than that, but it's just not a malignant lesion.
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Right. So we're seeing a lesion.
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So this is a 28-year-old with visual loss, right?
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Not something we're going to have to really want to do
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something about. So when you start thinking along and say,
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okay, we got the lesion.
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Now what? So that's when we kind of get back.
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And as I say,
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most of my reports and something like this are going to be
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describing the anatomic relations so that somebody can
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start thinking about that. This thing, for example,
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is in the middle fossa, right?
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Now, we talked about the cavernous sinus.
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So this is way out there, right?
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It's on the lateral side of that carotid, okay?
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It's in the middle fossa.
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So we know. The cavernous sinus is involved.
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Okay.
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The super cavernous carotids are displaced and encased.
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And encased, right? So they're going through the lesion,
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okay. The anterior cerebral complex,
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see that right there is right on top of the lesion.
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So if you're pulling it down from below,
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you got to wonder, well, if I'm going to do that,
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can I do that without damaging the anterior
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cerebral complex? So right there.
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So that is a very important relation.
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You can see right here these anterior cerebral
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complex kind of riding on top of it.
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So that's an important thing to know.
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And also the posterior communicating.
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So here's one going right through the lesion.
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Okay?
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So you're going to have to be looking
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out for these things.
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If we're trying to get rid of this or decompress it,
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at least that's going to be the goal.
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Maybe not completely removal because we
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said it's in the cavernous sinus,
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but if we can decompress the optic apparatus,
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I think transsphenoidal approach is probably going
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to have a role here, but it's going to be tough.
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You're right up against the basilar.
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Right? So you may not want to get all the way back here,
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take some of this out, decompress the optic apparatus,
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and then you still have a transcranial approach,
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depending on how successful you are with that.
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Okay, but this guy, we're not going to let him go blind.
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So something's going to need to be done.
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If it turns out to be a prolactin secretor,
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medically shrinking it down, boy, that's the best option.
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If that's not what's going on here,
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then there are surgical options,
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but it may take more than one.
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But probably because a sellar is so big,
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probably start out from below,
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kind of suck it out from right,
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see what the consistency of it's.
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Like wood, that's not going to work,
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but at least you try to.
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If it's very soft and suckable,
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you may do better than you think.
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And this supercellar portion can prolapse down,
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at least provide some measure compression.
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Yeah, a couple of just kind of summary points.
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There is some anterior extension,
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some presellar extension. As we said, it's intracellular.
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Supercellar. There's retroclival or retrocellar extension.
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And there is infracellar extension.
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If we look at this thing really carefully
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in the axial projection, we follow it.
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Sorry, I'm going up. Let's go down.
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We follow it down, down the carotid.
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Termini are splayed. Let's keep going.
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It's going a little bit off to the right.
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And wow, right there. It's in the Nasopharynx,
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which is unusual.
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And let's look at the Sagittal projection to see if
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that's real. Let's go over to the better side.
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And we can see a clear plane of hypointense separation
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right there. I'm going to make it a little brighter.
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And now let's go over to the other side.
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And you'll see it just wiped out the bone.
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And boom, it's gone right into the Nasopharynx,
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right next to the fossa of Rosenmuler.
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So it has infracellular extension.
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And then finally,
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as I've described to you in other Vignettes,
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instead of the lateral cavernous sinus wall,
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which is right here being a line,
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this black line right here.
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With gray on one side and white on the other.
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It's an interface.
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It's simply an interface with a gray mass abutting it
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so it's no longer a line with white underneath.
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It an obvious sign of cavernous sinus extension.
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Now, one more thing Dr.
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Pomerance was talking about.
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Let me give you the drive back.
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So one thing you might want to do,
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depending on the prolactin things,
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is do you want to biopsy it to figure out what's
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going on before we even get involved?
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Kind of easy biopsy, right?
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It's in the sphenoid. It's really taken out the sphenoid.
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Yeah, I don't want to biopsy.
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You could ENT could do it for you.
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Okay.
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And maybe that'll make you a little smarter when
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you're trying to figure out what to do,
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what the consistency is going to be,
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what other treatment options you have.
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So this is kind of going to present itself right
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out there. So that's another consideration.
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I'll make one other point that I know you love,
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and because this lesion is pretty
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gray and kind of solid looking,
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one of the thoughts you have here is this a weird
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meningioma that's just wiped out the.
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Pituitary gland, which is unusual,
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usually can separate out the gland.
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But I know you love this sign of carotid encasement and
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just kind of compression kind of crushing down the
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carotids and the carotid flow voids
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and their shape is maintained.
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So that really goes against the diagnosis of meningioma,
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as does the enhancement. Granted,
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it's enhancing quite a bit,
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but not as much and not as intensely as a meningioma,
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which has the mother in law sign.
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Likes to come early, likes to stay late.
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Intense enhancement early on. Well, the other thing is,
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well, okay,
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meningioma from where meningiomas start at areas
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of blood supply at particular places,
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meaning the tuberculum sellae would have to be the origin.
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And you don't see a lot of hyperostosis
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stuff like that there.
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You think it'd be worse if it was
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really coming from there.
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Which is kind of where it would have to be started
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to get into the sellar and grow like that.
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So meningiomas location, location, location.
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Right? Because they don't just start all over the place.
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Right. There's particular places.
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And there and the surgery for them is to get to
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the blood supply first, devascularize them.
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So finding the origin of a meningioma is really and the
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tuberculum sellae meningioma is really in this differential.
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So I think when you're reporting this in the conclusion,
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you have to say,
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most compatible with pituitary macroadenoma,
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with other differential diagnostic considerations
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unlikely. And I think it's time to move on.
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Shall we?
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