Publication:
A Rare Case of Sporadic Optic Pathway Glioma in a 7-year-old Female

creativeworkseries.issn1812-2027
dc.contributor.authorGupta, S
dc.contributor.authorSinha, U
dc.contributor.authorRaj, A
dc.date.accessioned2026-01-14T07:45:58Z
dc.date.available2026-01-14T07:45:58Z
dc.date.issued2024
dc.descriptionGupta S,1 Sinha U,2 Raj A3 1Department of Physiology All India Institute of Medical Sciences (AIIMS), Gorakhpur (Uttar Pradesh), India 2Department of Radio-diagnosis 3Department of Ophthalmology All India Institute of Medical Sciences AIIMS, Patna, Bihar, India
dc.description.abstractABSTRACT Sporadic optic pathway gliomas (OPGs) are uncommon and have greater predisposition to severe clinical presentations and complications. Severe visual impairment is the most frequent presentation. The treatment is based on multiple factors and needs to be individualized. Precise assessment of visual function is one of the important factors to plan the management. We present a case of sporadic OPG in a 7-year-old female with severe visual decline. Visual functions were assessed ophthalmologically and electrophysiologically. Diagnosis was confirmed on the basis of clinical, radiological, histopathological and electrophysiologic findings. Surgical resection was planned owing to the poor visual functions and the mass effects. Patient is on regular follow-ups with no signs of deterioration so far. Appropriate visual assessment is crucial in young children with sporadic optic pathway glioma for planning the mode of treatment. Surgical resection in cases with severe visual impairment is helpful, however, irreversible visual impairment remains irremediable. KEY WORDS Optic pathway glioma, Sporadic, Visual
dc.identifier.urihttps://hdl.handle.net/20.500.14572/4263
dc.language.isoen_US
dc.publisherKathmandu University
dc.subjectOptic pathway glioma
dc.subjectSporadic
dc.subjectVisual
dc.titleA Rare Case of Sporadic Optic Pathway Glioma in a 7-year-old Female
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage498
oaire.citation.startPage495
relation.isJournalIssueOfPublicatione11bafba-6525-4c58-88d9-4eff4919cf29
relation.isJournalIssueOfPublication.latestForDiscoverye11bafba-6525-4c58-88d9-4eff4919cf29
relation.isJournalOfPublicationa782b7ff-cf89-4178-ad1c-11ed89cfe1bd

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