Abstract
ONSM typically affects middle aged women. Ophthalmologic presentation in the vast majority of patients consists in the classical features of optic neuropathy. The vast majority of patients exhibit a variable loss of vision and/or visual field, almost always accompanied by funduscopic evidence of optic nerve pathology. Optic nerve involvement presents in one half of those affected either as a disc swelling or optic atrophy. Careful examination will virtually always reveal a reduced amplitude and velocity of pupillary light reaction, a so-called relative afferent pupillary defect. Proptosis and motility impairment may develop; however they usually are only of moderate degree. Disease progression is slow, but in many cases results in blindness if left untreated. While in the adult patient population, prognosis quo ad vitam is excellent, childhood ONSM runs a more aggressive course and may be a sign of neurofibromatosis.
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Pitz, S., Wilhelm, H. (2008). Clinical Presentation. In: Jeremic, B., Pitz, S. (eds) Primary Optic Nerve Sheath Meningioma. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-77558-4_2
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DOI: https://doi.org/10.1007/978-3-540-77558-4_2
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