Interactive Transcript
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We're going to segue from our infectious etiologies of
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extradural disease into the neoplastic category.
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You've seen the discussion of
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nerve sheath tumors before,
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both when we were dealing with intradural intramedullary
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lesions, as well as intradural extramedullary lesions.
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I just want to refresh your memory that in 15% of cases,
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the nerve sheath tumor in the spine may be completely
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extradural and in another 15%, it may be the so called
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dumbbell lesion, which has both an intradural compartment
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as well as an extradural component.
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Here, for example,
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is a patient who has a cystic schwannoma in the lumbar spine.
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It is causing enlargement of the neuroforamen on the
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right side and is displacing the
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thecal sac to the left side.
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Do not be confused by the bright signal
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on the T2-weighted scan.
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Remember that we've seen lesions that are bright on
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T2, which still shows avid contrast enhancement.
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So this is not a cyst.
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This is in fact a tumor.
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And in this case, a schwannoma in the neuroforamen.
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Here it is on the pre-contrast T1-weigghted scan.
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Contrast that with this case that was also shown when
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discussing intradural extramedullary lesions.
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Here we have the schwannoma, which is extending from the
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intradural extramedullary location into an extradural
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location in the left neuroforamen.
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So again,
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if we look at this purely on the T2-weighted scan,
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it is very bright. We might say, well,
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could that just be a big cyst?
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As you note on the post-gadolinium enhance scan, however,
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this lesion is solidly enhancing. And right
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about here is our border with the dura.
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So we have a component that is intradural extramedullary,
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as well as the component that is extradural
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and extending out into the far neuroforamen.
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So an intradural extradural dumbbell schwannoma.
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I also showed this slide in the previous talk on
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intradural extramedullary lesions to show that the
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patients who have neurofibromatosis type II might
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have lesions intradural, as well as extradural.
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In this case,
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big lesions in an extradural location, actually,
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intramuscular even, as well as some that
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are intradural but extramedullary.
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And this is part of the neurofibromatosis type II
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syndrome, also known as MISME for
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Multiple Inherited Schwannomas,
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Meningiomas, and Ependymomas.
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Neurofibromas are more characteristically found in patients who
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have neurofibromatosis type I.
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And these lesions as well may be extradural
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or intradural. Sometimes, they may be associated also
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with intramedullary lesions
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like neurofibromatosis type II,
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the latter causing ependymomas, whereas neurofibromatosis
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type I, associated with astrocytomas of the spinal
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cord. The dural ectasias and arachnoid
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cysts and scalloping are also a manifestation
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of neurofibromatosis type I. In children,
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we also consider the neuroblastoma, ganglioglioma lesions that
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occur in a paraspinal location.
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In this case,
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we see them in the anterior paraspinal location.
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However, they may be laterally located or they may extend
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into the neuroforamena. This big lesion,
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although predominantly anterior to the spinal canal, we
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see it goes into the neuroforamena, and in that way, can
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actually cause compression of the thecal sac.
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This, by the way, is the kidney.
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So let's not be distracted by that.
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So neuroblastomas and ganglioneuromas and gangliomas are
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lesions that will vary in the histology depending upon
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the age, with the neuroblastomas being those
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that occur in the youngest age group.
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On the axial scan, we see this big lesion
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here representing the ganglioneuroma.
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