ArticleCase reports in ophthalmology2012
Optic nerve sheath meningioma in the first decade of life: case report and review of the literature.
Article in Case reports in ophthalmology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed, 21 citations in OpenAlex.
- Primary and Secondary Optic Nerve Sheath Meningioma.Journal of neurological surgery. Part B, Skull base · 2021Article
- [Primary meningioma of the optical nerve sheet in infancy as initial presentation of neurofibromatosis type 2].Der Pathologe · 2019Article
- Variable structure and function relationship of compressive optic neuropathy at the time of diagnosis.Clinical ophthalmology (Auckland, N.Z.) · 2019Article
- MR imaging of brain pilocytic astrocytoma: beyond the stereotype of benign astrocytoma.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2017Review
- Central Retinal Vein Occlusion in a Childhood Optic Nerve Tumour.Neuro-ophthalmology (Aeolus Press) · 2016Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND/
aimTumors of the optic nerve are mostly either optic nerve gliomas or optic nerve sheath meningiomas (ONSMs). While gliomas occur in children, most meningiomas are slow-growing tumors affecting middle-aged individuals with progressive visual loss, proptosis, disc edema and optociliary veins on fundus examination. ONSMs are extremely rare in children, with only 14 cases reported in children under the age of 10 years. The purpose of this study is to describe an additional case and review clinical, radiologic and histopathological findings that can help differentiate such tumors in children and allow an early and accurate diagnosis. CASE REPORT: An 8-year-old girl had a 2-year history of progressive proptosis and total visual loss on the right side. A computed tomography scan revealed a well-defined intraconal mass with perioptic calcification. Magnetic resonance imaging showed a tumor surrounding the optic nerve and extending intracranially, with enhancement following gadolinium injection. The patient was submitted to fronto-orbital craniotomy for complete tumor excision. Histological studies identified the neoplasm as ONSM.
conclusionsThough unusual, ONSMs may occur in children and, in these cases, present a much more aggressive behavior than in adults. ONSM should therefore be differentiated from optic glioma in children because of its aggressive behavior and need for different treatment modalities.
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