Interactive Transcript
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Another of the intrinsic lesions of the
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optic nerve is the optic nerve glioma.
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This is a tumor which is seen in the pediatric
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population largely, secondary to neurofibromatosis type 1.
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Here we have a patient who has enlargement of the optic nerve
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within the optic nerve sheath,
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demonstrated on the T2-weighted imaging.
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We separate the optic nerve enlargement
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from the sheath on the T2-weighted scan.
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So, here is the optic nerve enlargement,
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separate from the optic nerve sheath.
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This second case, we see that the patient has the
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bilateral involvement of the optic nerves,
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and we are starting to see thickening of the optic chiasm, as well.
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On the FLAIR image,
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we see that the chiasm is markedly enlarged and
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the tumor is going into the optic radiations,
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the temporal lobe optic radiations. And from there,
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could extend even to the occipital lobes.
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This is a low-grade astrocytoma, pilocytic astrocytoma,
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associated with neurofibromatosis type 1.
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In general, this is very difficult to treat,
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and therefore, it is merely observed rather than addressing surgically.
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Here's a patient with a CT scan, demonstrating marked
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enlargement of the optic nerve sheath complex
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in a patient who had optic nerve glioma.
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One of the features of neurofibromatosis is something
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that we hear about a lot but never show on imaging.
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This is an image of Lisch nodules.
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These are these brown pigmentation on the iris of the globe.
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And this is one of the primary criteria
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of neurofibromatosis type 2.
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There are no imaging features on CT or MRI
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scan that correlate with Lisch nodules.
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Remember also that Café-au-lait spots and axillary
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freckling also constitute some of the major criteria
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of neurofibromatosis type 1,
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as well as plexiform neurofibromas.
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So the primary criteria for neurofibromatosis include
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six or more café au lait spots, two or more Lisch nodules,
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axillary freckling, an optic pathway glioma,
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first-degree relative with neurofibromatosis,
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a plexiform neurofibroma or bone dysplasia.
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Now, that bone dysplasia often affects the greater wing of
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the sphenoid, and therefore can lead to proptosis as you
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have herniation of brain tissue through the greater ring
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of the sphenoid, or what is characteristic of neurofibromatosis,
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which is pulsatile exophthalmos,
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that is, that CSF pulsation in the brain is transmitted to the orbit
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and the globe is seen to pulse in and cause exophthalmos.
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Within the orbit itself,
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not only do we have the possibility of bony
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dysplasias and optic nerve gliomas,
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you may have a plexiform neurofibroma of the fifth
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cranial nerve that can infiltrate the orbit.
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You can have remodeling of the walls of the orbit.
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You can have expanded CSF space into the orbit,
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enlarged foramina of the orbit from neurofibromas
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of the cranial nerves,
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and you may have elongation of the globe itself,
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one of the causes of macrophthalmia, so-called buphthalmos.
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