Interactive Transcript
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with a pancreatic mass, which
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we have to characterize now.
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And I will start with T1 fat-suppressed,
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non-contrast-enhanced images here.
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And we see this expansive large mass in
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the pancreatic tail, which shows multiple
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areas of heterogeneous T1 hyperintensities
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along with the periphery of this lesion.
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So that gives us an idea that possibly
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this lesion actually has some internal
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hemorrhages or hypertense content.
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And if we correlate this with T2-weighted images,
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we find that this, this entire thing which was
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looking T1 hyperintense actually is T2 hyper
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intense, so that further reinforces our thought
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that it is possibly hemorrhagic content here.
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But this tumor looks like
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necrotic at multiple locations.
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It is very big espine cell involving the
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pancreatic tail in a young female patient.
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So that is a daughter tumor.
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That means it is SPN.
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So, let us see how it behaves
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in the arterial phase.
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On the arterial phase, we can see
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most of the tumor is not enhancing,
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only the periphery is enhancing.
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And then, if we go to the venous
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phase, we can see it better, the non
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enhancing part and enhancing part.
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But if we compare it with the, the one we
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started with the arterial phase, if we see the
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enhancement pattern on the arterial phase, the
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periphery of this lesion is enhancing like a rim.
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Like, there is a claw formed here, and
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almost everything along with the periphery is
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enhancing, but the center is not enhancing.
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It's mostly necrotic, mostly it
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is replaced by hemorrhagic tissue.
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The point is, given the age, given
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the presentation along with the tail,
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given the gender, it favors it as SPN.
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But sometimes the same appearance can
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be seen with neuroendocrine tumors.
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Those are non-functional.
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They can grow up to this extent and
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they can undergo necrosis as well.
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But usually that necrosis is not
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that striking as in this case is.
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So, in the case of neuroendocrine tumor,
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when it is necrotic, you will still see
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some of the enhancing soft tissue, and that
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will enhance more during the arterial phase.
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And then, non-functional neuroendocrine
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tumor, still you can have tumor markers.
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And patient age group can be
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different, patient can be male as well.
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But in this particular patient, given this
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patient's presentation and the appearance of
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the tumor, uh, we gave the diagnosis of SPN, and
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it was proven on the postoperative pathology.
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