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Optic Nerve Glioma, NF1

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We are continuing our analysis of

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intraconal lesions of the orbit.

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This next patient presented with left-sided visual loss.

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As we look at the T1 and T2 weighted

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scans of the brain MRI,

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we notice an asymmetry in the size of the left optic

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nerve compared with the right optic nerve.

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We see that the left optic nerve caliber

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is wider than the right optic nerve.

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This is true both on the T2-weighted scan

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as well as the T1-weighted scan.

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We also note that the normal signal intensity of the

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optic nerve, which should look like white matter,

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is brighter

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on the T2-weighted scan.

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With respect to optic nerve sheath lesions,

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we want to make the distinction between that,

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which is respecting the optic nerve versus the meninges

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that surround the optic nerve sheath.

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Because the differential diagnosis is an optic nerve glioma

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versus an optic nerve meningioma.

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Remember that the optic nerve is not a peripheral nerve.

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It's actually a portion of white matter from the brain,

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and therefore,

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we do not get schwannomas of the optic nerve.

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We get optic nerve gliomas or astrocytomas,

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and the vast majority of these

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are pilocytic astrocytomas.

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The tumor of the optic nerve sheath is a meningioma

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and this will generally spare the signal

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intensity of the optic nerve.

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Let's look at the additional sequences on this patient.

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As we scroll further inferiorly,

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we note that there is a large mass

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along the right side of the neck.

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This mass is quite heterogeneous and infiltrates

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a great portion of the right side of the neck.

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We identify the internal carotid artery.

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And we identify the vertebral artery,

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and we see how closely opposed the tumor is to these blood vessels.

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This is a multiloculated lesion in the right side of the neck.

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If we scroll further inferiorly,

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we see that it will continue down the neck,

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extending to the subcutaneous tissue,

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as well as infiltrating the fat,

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as well as infiltrating the musculature,

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while it also infiltrates the carotid sheath.

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For those with good

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analytical tools,

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one might also note that the neuroforamen on the right side,

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at this cervical spine level, is enlarged.

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Further inferiorly,

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we note that there is an additional lesion that is

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infiltrating around the clavicle

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and between the clavicles.

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And an additional lesion in the right axilla.

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This is a patient who has neurofibromatosis type 1 with

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plexiform neurofibromas, affecting the right side of the neck,

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as well as the anterior chest wall and the right axilla.

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Now, when we consider the lesion in the orbit,

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it makes a lot more sense.

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This is a patient who has an optic nerve glioma as

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part of the neurofibromatosis type 1 spectrum.

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There are seven major criteria for neurofibromatosis type 1.

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They include café-au-lait spots,

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axillary freckling, lisch nodules,

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plexiform neurofibromas, optic nerve pathway gliomas,

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a family history of neurofibromatosis,

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and bony dysplasia.

Report

Description

Faculty

David M Yousem, MD, MBA

Professor of Radiology, Vice Chairman and Associate Dean

Johns Hopkins University

Tags

Syndromes

Pediatrics

Orbit

Neuroradiology

Neuro

Neoplastic

Neck soft tissues

Musculoskeletal (MSK)

MRI

Head and Neck

Carotid Space

CT

Brachial Plexus

Bone & Soft Tissues

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