Interactive Transcript
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We've been dealing with intraconal lesions and
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have been focusing on the optic nerve.
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So we've seen cases of optic nerve gliomas,
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both isolated as well as with neurofibromatosis type 1.
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And then, we moved to optic neuritis
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and we saw cases of multiple sclerosis with optic neuritis.
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We talked about idiopathic optic neuritis,
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where it is unassociated with demyelinating disorders.
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And then, we talked about
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Neuromyelitis Optica Spectrum Disorder, NMOSD.
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I'd like to now continue with the discussion of
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intraconal lesions, but move from the optic
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nerve to the optic nerve sheath.
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Interestingly enough,
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optic nerve sheath meningiomas tend to present
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with visual loss earlier and with more severe
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visual loss than lesions of the optic nerve itself.
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So it is one of the distinguishing features that
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a patient with optic nerve meningioma tends to
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have worse visual loss than a person with optic nerve glioma,
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in part because of the low grade nature of
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the optic nerve glioma, which, as I said,
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is a grade 1 pilocytic astrocytoma.
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So, this patient presented with visual loss in the right eye.
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As we scroll the T2-weighted and post-gadolinium scans,
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we see that, once again, we have a lesion that is
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affecting the optic nerve sheath complex.
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On the T2-weighted scan, it shows low signal intensity,
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and it is relatively extensive,
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going through the orbital portion of the optic nerve sheath complex.
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The post-gadolinium-enhanced images are somewhat
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different than what we've seen previously,
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in that it appears as if the optic nerve itself
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can be separated from the optic nerve sheath lesion.
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So, on the post-gad fat-suppressed scan,
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we are seeing contrast enhancement,
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but it looks as if this is extending along the
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length of the optic nerve sheath complex.
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However, the optic nerve itself has normal signal
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intensity, is not what is enhancing.
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Okay, I'm going to pull down the T1-weighted scan
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post-contrast with fat suppression.
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And here, as we scroll the images,
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we find a unique characteristic of this lesion.
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I'm going to stop on this image,
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which is midway through the orbit.
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Note that the optic nerve itself is not enhancing,
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and yet we have all of this fluffy enhancement
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around the optic nerve within the optic nerve sheath.
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Contrast this amount of enhancement with
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the normal optic nerve sheath complex,
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which may only show little specks of enhancement
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of the optic nerve sheath.
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So this is a lesion of the optic nerve sheath,
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but not the optic nerve.
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And the most common of these lesions is the optic nerve meningioma.
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One can get other lesions that affect the optic
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nerve sheath, including things like sarcoidosis
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or subarachnoid seeding,
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or other inflammatory lesions, including idiopathic,
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orbital inflammation, or pseudotumor.
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Meningiomas of the optic nerve may occur within the
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orbit or they may extend along the
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optic nerve from the skull base.
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One of the things to be very concerned about
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is making sure that the lesion is emanating
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directly from the optic nerve sheath complex
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within the orbit, as opposed to the skull base.
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Why is this important?
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The most common location for skull base
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meningiomas that extend along the optic nerve
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is the planum sphenoidale.
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This is this region of the skull base.
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From this region,
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an optic nerve can be affected bilaterally via the optic canal.
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Having bilateral meningiomas is a very bad
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prognostic sign because of bilateral visual loss.
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So when one sees an optic nerve meningioma,
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one wants to make sure that it's primarily from
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the orbital portion and not from the
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skull base where the potential is,
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that may extend into the contralateral optic nerve,
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leading to binocular blindness.
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