Interactive Transcript
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You.
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So in the next seven or ten minutes,
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I'm going to be discussing
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how do we approach adult intraxial tumor and
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especially focusing on tumor mimics.
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You know, non-neoplastic lesions
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which could look like a tumor.
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So if you look at the definition of tumor,
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it's a Latin word for swelling and
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it's not really synonymous with cancer or neoplasm,
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to which we,
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majority of the times,
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confuse with or misuse it for.
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Here is an example of a lesion which could look
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like a tumor and a non-neoplastic lesion.
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A 41-year-old male presenting with altered
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mental status and expressive aphasia.
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In the emergency department you can see there is a lot
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of vasogenic edema and swelling in the left brighter
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lobe which shows some peripheral kind of thick left
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meningeal enhancement and also has a couple of small areas
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of restricted diffusion which kind of conform to this
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smaller necrotic regions within this lesion.
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And if you look at my impression,
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I say the possibility of an infection or inflammatory
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disease process cannot be excluded.
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A granulomatous disease process is also a possibility.
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A tumor, when I say tumor over here,
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what I mean is a neoplasm seems less likely,
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though focal leptomeningeal metastatic disease
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cannot be completely excluded.
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A venous infarct also seems less likely.
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But I'm considering that and that kind of report when
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I look at that there is a lot of hedging going on.
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I'm not really focusing on one particular differential
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diagnosis because of the appearance of this lesion.
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But I am favoring infection as a very high possibility
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considering especially those small areas of restricted
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diffusion in the necrotic portion of the lesion.
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And this is what happens.
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This patient was managed conservatively and within a
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few weeks you can see the patient comes back to the
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emergency department again and now
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with a much larger lesion,
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clearly increased areas of enhancement and larger areas
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of this necrotic cystic part which
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is showing restricted diffusion.
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And when I see a transformation that quickly
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within a few days or a couple of weeks,
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that's much more concerning for an infection.
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And based on this restricted diffusion,
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this one turned out to be a pyogenic abscess.
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Another example over here, a thick irregular necrotic
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mass in the posterior left frontal lobe.
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And if you look at the differential diagnosis,
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it could be anywhere from a stroke,
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a subacute infarct or hemorrhage could look like that.
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An infection and abscess could look like that.
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Neoplasm I am considering very highly glioma based
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on the irregular necrotic appearance of this mass.
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But metastasis and lymphoma is in the
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differential diagnosis now also.
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Considering cumifactor demyelinating lesion
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in the differential diagnosis.
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But if I look at a scan done just five
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days prior to this baseline scan,
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you can see this lesion again evolved very quickly.
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Five days ago,
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all you could see is that swelling and with some
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peripheral minor enhancement along the cortex over here.
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And within five days, this lesion has increased in size,
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is showing a lot of tissue breakdown and necrosis.
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And if I look at the history,
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this is a young patient with infective endocarditis.
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And with that history and with that quick evolution,
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if I look at the diffusion-weighted images,
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it's very clear that this is really a pyogenic abscess.
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The reason being it's showing restricted diffusion in
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that central necrotic cystic part of the lesion.
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Right. So that turned out to be a pyogenic abscess.
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So pyogenic abscesses typically will show restricted
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diffusion in the central necrotic part.
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Two different patients, two different entities.
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Over here in the upper panel,
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you can see peripheral thin,
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relatively regular rim of enhancement showing restricted
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diffusion in the central necrotic portion.
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The one in the lower panel also has thin rim
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of enhancement and central necrosis,
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but without restricted diffusion.
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And the one in the upper panel
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turned out to be an abscess,
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whereas the one in the lower panel
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turned out to be a glioblastoma.
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So it's very important to look at
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diffusion-weighted imaging.
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Another example over here is a patient who
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presented with a peripheral thick,
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irregular rim enhancing lesion showing some
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restricted diffusion in the central portion.
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And within a week,
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you can see the lesion grew very quickly,
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shows much more increased swelling, edema, mass effect,
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and also has restricted diffusion,
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but more at the nodular peripheral
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component of the lesion.
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Another separate lesion is seen in
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the left cerebral hemisphere,
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and this one turned out to be a fungal abscess and
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aspergillosis so abscesses typically pyogenic abscesses
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will show restricted diffusion
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in the central necrotic part,
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whereas fungal abscesses may show restricted diffusion
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along the peripheral nodular component
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of the abscess also.
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But once I see that quick evolution
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and restricted diffusion,
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you have to consider an infection as a tumor mimic in a
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case like that. So solitary necrotic intraxial masses,
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I can divide them into glioma,
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solitary metastasis abscess or Lymphoma,
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and other entities such as granuloma tuberculoma
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and tumefactive demyelinating lesions.
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And the first thing I want to look at on an imaging,
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if the patient especially has fever and
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is showing restricted diffusion,
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that kind of favors the diagnosis of an abscess.
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On the other hand,
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gliomas if there is especially older individuals,
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multifocal or multicentric disease and
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non-enhancing cortical involvement.
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An infiltration going beyond the
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enhancing part of the tumor.
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Whether you diagnose that with Mr perfusion or Mr
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spectroscopy or on Flare imaging is always indicative
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of a high-grade glioma in an adult patient.
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When I'm trying to consider solitary metastatic lesion
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always look for other enhancing lesions,
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disproportionate edema, history of primary malignancy.
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For example,
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if the patient has lung cancer node kind
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of favors solitary metastasis,
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usually metastasis they don't infiltrate
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beyond the enhancing tumor margins.
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And that's another thing if you can use Mr spectroscopy,
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MR perfusion to diagnose that.
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On the other hand lymphoma and other granulomatous
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tuberculomas they are usually seen in immunocompromised
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patients and may show incomplete ring of enhancement.
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Here is an example adult patient presenting
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with progressive left-side weakness.
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And you can see there is a large tumor-like lesion in
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the right basal ganglia with swelling and mass effect.
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But if you look at the post-contrast images, there is
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incomplete rim of enhancement. And once we see that,
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we know that this is not a tumor,
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it's a tumefactive demyelinating lesion.
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As you can see a month later there is almost complete
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resolution of the lesion with conservative management.
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Another example over here in a 35-year-old individual
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presenting with headache and foot drop,
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numbness and tingling in the hand.
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And what we see on imaging is heterogeneously enhancing
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tumefactive lesion in the right parietal deep
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periventricular white matter has some edema swelling,
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some restricted diffusion.
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But if you look at the post-contrast images, the majority
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of the enhancement is almost like an incomplete ring
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of enhancement. And this is two months later.
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You can see the enhancement kind
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of is changing rather quickly.
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The edema actually has increased and this is
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three years later complete resolution.
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This is another example of a tumefactive
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demyelinating lesion. Now,
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one of the things we do to differentiate tumefactive
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demyelinating lesion from a neoplastic lesion
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such as a glioma. Two different patients,
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one in the upper panel showing you a mass in the left
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cerebral hemisphere whereas the one in the lower panel
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has a mass in the right cerebral hemisphere.
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If you look at the diffusion,
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not much to differentiate between
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the two post-contrast images.
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The one in the lower panel is showing
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you an incomplete rim of enhancement.
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There is some mild marginal enhancement even
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for the patient in the upper panel.
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If I show you the perfusion maps, it's much more clear
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which one is a neoplasm and which one is not perfusion.
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The one in the upper panel is showing you much more
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increased blood volume suggesting that this is a
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neoplastic lesion whereas the one in the lower
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panel is showing you very low blood volume.
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And this is what we typically see with TB to
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demyelinating lesions which could look like
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a high-grade glioma on imaging.
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But if.
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Look at the perfusion,
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they are usually very low on blood volume.
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This is what is already known.
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We published it many years ago looking at
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differentiating tumefactive demyelinating lesions
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from high-grade gliomas based on perfusion.
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Typically,
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high-grade gliomas will show high blood
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volume and also high leakiness,
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whereas tumefactive demyelinating lesions will show low
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blood volume and low leakiness on the perfusion scans.
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And that's one way to differentiate tumefactive
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demyelinating lesions from high-grade gliomas.
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Now,
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sometimes we do fall into a case like this where
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it clearly looks like a high-grade glioma.
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Even on perfusion maps,
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you can see very high blood volume.
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And luckily, we don't see these cases that often.
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This one turned out to be a tuberculoma.
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And I think the only thing we can see in a
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case like that, retrospectively maybe,
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is that thin rim of T2 dark signal which probably
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pointed that this could be something
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other than a glioma. Again,
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I don't expect anybody to make a diagnosis of
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tuberculoma based on the initial baseline
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imaging in a case like this.
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But once in a while we do fall into that where you have
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cases such as tuberculoma presenting like a lesion which
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almost looks like a very high-grade glioma or a GPM.
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This is another example,
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another entity which can look like a tumor.
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Here's a patient sent to one of our neurosurgeons
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for a biopsy to confirm a tumor.
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And when I looked at the scan,
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there's a very well-defined lesion in
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the splenium of the corpus callosum.
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If you look at the T1 weighted images,
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it's actually very bright on T1 weighted images not
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showing much contrast enhancement and showing some
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susceptibility blooming at the periphery of this lesion,
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low in blood volume.
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And this one turned out to be actually a cavernoma,
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right?
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So vascular lesions such as cavernomas
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could mimic a neoplasm on imaging.
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Another entity which we see maybe five to seven cases a
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year in a busy neurosurgical practice which can mimic
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a neoplasm is vasculitis. Here is an example,
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a solid-enhancing,
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heterogeneously enhancing mass in the left frontal lobe
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which was sent for biopsy to confirm the diagnosis
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of a suspected diagnosis of a glioma.
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And when we look at SWI,
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it's showing you areas of susceptibility blooming
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in the central part of the lesion.
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But more importantly,
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DSC-T2* perfusion analysis showed that the lesion
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in fact showed low blood volume even in the regions
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which were not showing susceptibility blooming.
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And this is another way to differentiate a high
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grade glioma from a non-neoplastic entity.
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For example,
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this one turned out to be cerebral amyloid angiopathy
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on histopathology and tissue diagnosis.
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