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Summary of Extradural Neoplasms

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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.

Report

Description

Faculty

David M Yousem, MD, MBA

Professor of Radiology, Vice Chairman and Associate Dean

Johns Hopkins University

Tags

Spine

Neuroradiology

Neoplastic

Musculoskeletal (MSK)

MRI

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