Interactive Transcript
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So let's talk about perio, lymphatic nodules.
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Now again, so these are nodules which are gonna live
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along the lymphatics.
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And so here again is my diagram.
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So these nodules are gonna be along the interloper, septa,
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subpleural lung, sometimes central lo core structure
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and along the bronchovascular tree.
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And so as opposed to random nodules
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where they're like really all over the place, like tropic,
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these perilymphatic nodules tend to cluster.
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Let's just show you example here.
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So here's example
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of these nodules along the intra lo receptor subpleural lung
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along the bronchovascular tree.
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But notice on this axial slice nodules in the more center
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mid portion of the lung from an
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anterior posterior direction.
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There's a lot of nodules here,
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but anteriorly especially right here, kind more peripherally
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and laterally, there are almost no nodules.
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And then posterior, there's just a few nodules.
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So perilymphatic nodules really like to do this,
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especially sarcoidosis, which is gonna be the first thing
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that you think about when we see perilymphatic nodularity.
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Here's our differential diagnosis for paralympic nodularity,
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but again, most of the time it's gonna be sarcoidosis,
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whether primary or secondary.
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Remember there are secondary causes of sarcoidosis.
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People act like they know sarcoidosis.
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They're like, oh, that's just sarcoidosis.
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But sarcoidosis is like very esoteric.
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No one really knows what causes sarcoidosis.
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It's probably the same endpoint
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or same phenotype of many different stimuli, which then lead
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to the same imaging morphology
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and same pathological abnormalities that we see.
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And that's why there are both idiopathic sarcoidosis cases
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and secondary sarcoidosis cases.
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But um, bottom line, the more I learn about sarcoidosis,
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the more I realize I don't really understand.
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Sarcoidosis. Very, very interesting.
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One of the secondary causes of sarcoidosis,
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which is well defined from occupational exposure,
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is chronic beryllium disease or borreliosis from.
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So if someone works in aerospace
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or manufacturing of, of certain types of lamps
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or just maybe works in, in a place that uh,
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maybe minds this stuff,
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then obviously you would think about borreliosis.
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But most places don't have a bres
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clinic or beryllium clinic.
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If you do, then obviously it would be something you include
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in differential diagnosis.
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So paralympic nodules, sarcoidosis,
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sarcoidosis, sarcoidosis.
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And every once in a while you just wanna make sure you're
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not dealing with a case of lymphocytic carcinomatosis.
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But usually most of those cases they manifest
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with interocular, septal thickening
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and some associated nodularity along the interlobular septa
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rather than the para lymphatic nodularity being the major
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finding on that CT scan.
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Also, when you have lympho genetic carcinomatosis,
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very commonly they're gonna have other
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manifestations of malignancy.
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You're gonna have like maybe even like a big tumor,
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which is the primary tumor.
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And then you're gonna have adjacent
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lympho, genetic carcinomatosis.
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So it's spreading into lymphatics,
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or we're gonna have like macroscopic nodules within the
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lungs which spread their hematologist
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and now are extending into the interlobular
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septa and the lymphatics.
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So usually it's not a diagnostic conundrum in
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that alternative diagnostic consideration of lympho genetic
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Carcinomatosis.
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So more sarcoidosis here.
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Paralympic nodularity, beautiful example.
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Again, they like the cluster sarcoidosis.
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I don't know why, but beautiful example
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of interocular sepup here.
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Rock blaster tree, visual nodularity, subpleural nodularity,
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just classic sarcoid sarcoidosis likes
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to be mid upper lung preponderant,
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but I certainly have also seen cases
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of basal predominant sarcoidosis.
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It's not as common, but it should not dissuade you from a
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diagnosis sarcoidosis just based on zonal distribution.
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Another example of sarcoidosis with mass like fibrosis here.
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So, so sometimes patients with sarcoidosis can start
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to evolve into a fibrotic pattern.
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And so very commonly you take a mass like morphology.
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And so we see that here on ct. This is just an MRI.
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This is just a vibe sequence with gadolinium contrast.
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So those of you guys who do a lot of cardiac MRI,
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you should probably look at these vibe sequences
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or your T one sequences, uh, carefully,
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especially after contrast.
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'cause I very common with MRI, you're looking
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for an infiltrative abnormality like cardiac sarcoidosis.
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And so if you're looking for cardiac sarcoidosis,
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you should probably look for pulmonary sarcoidosis as well.
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And this patient indeed had pulmonary sarcoidosis
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with very beautiful perilymphatic distribution.
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Here's the case of lympho genetic SP tumor.
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You see how this just looks different.
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So what, what's the diva of this CT scan here?
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You know, what's who? Who is the star of the show here?
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It's not nodularity is it?
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If you look carefully, it's gonna be the
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interlobular septal thickening.
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Sure, there's nodularity there superimposed on there.
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And sure it's perilymphatic
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because it's along the Interlobular septa.
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But the major finding here is that
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of interlobular septal thickening with concomitants.
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That's the secondary finding of interlobular,
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lymphatic nodularity.
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But this patient has like ular pleural fusions bilaterally.
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The patient history of malignancy.
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I mean, come on, no one would call this sarcoidosis.
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I think anyone who has any
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clinical experience at all in terms of diagnostic chest ct,
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the first thing that you'd be worried about,
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the first thing you would exclude would be
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that this is some sort of bad limited carcinomatosis.
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Maybe a lymphoma or some sort of odd leukemic infiltration
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or other inflammatory infiltrative abnormality.
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So yeah, this is not sarcoidosis, chronic brelin disease.
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I just wanna bring this up. And so sometimes
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these can look a little different.
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And so if we look at the CT scan very, very quickly,
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we might say, oh, there's just ground lass
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opacity all throughout the lungs.
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But you know that it's not brown lass opacity,
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it's more this fine granularity,
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which actually is clustering along fissures along the
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bronchovascular tree
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and in some areas along the subpleural lung.
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So this is a patient actually
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with chronic beryllium disease,
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but with a fine perilymphatic, nodularity.