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Developing Right Fusiform Optic Glioma

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This is an MRI of the brain

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in a two-year-old child

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with neurofibromatosis type 1.

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And at this young age,

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we don't see any significant signs

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of myelin vacuolization,

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possibly some subtle findings in the posterior

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aspect of the right globus pallidus.

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And otherwise,

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we're seeing some signal abnormality in the deep

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cerebellar white matter bilaterally.

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Now, the optic nerves at this time

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look normal in caliber.

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They're symmetric in caliber.

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If we look at the post-contrast imaging,

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on the right side,

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we're seeing a possible subtle focus

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of enhancement in the posterior orbital

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segment of the right optic nerve.

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But there's no significant tortuosity.

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And this could easily be written off

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as possible artifact or a passing vessel.

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But we know that patients

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with neurofibromatosis type 1

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have a significant

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predisposition to optic pathway tumors.

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Well,

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if we fast forward about seven or eight years,

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we can see there is asymmetric thickening of

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the right optic nerve throughout

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the entire orbital segment.

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We can see there's more tortuosity of the

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right optic nerve than the left because

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it goes out of plane and into plane.

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And this coronal image shows the fusiform

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enlargement of the right optic nerve

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as compared to the left.

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So, what started off as a subtle enhancement

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over eight or nine years becomes

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a very clear fusiform glioma.

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We don't know how every lesion will evolve.

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Some will get bigger over time.

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Some areas of enhancement in signal

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abnormality may dissipate,

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and some may stay the same.

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We don't know.

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But these are the types of findings that we're

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being asked to look for and being aware that

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not just an optic pathway glioma

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can occur in NF 1,

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but how it may look when it's more subtle,

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how it may evolve is important,

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and that's what my hopes are

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in showing this case.

Report

Faculty

Asim F Choudhri, MD

Chief, Pediatric Neuroradiology

Le Bonheur Children's Hospital

Tags

Pediatrics

Neuroradiology

Neuro

MRI

Brain

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