Please use this identifier to cite or link to this item: http://imsear.hellis.org/handle/123456789/71960
Title: A case of neurofibromatosis 1 presenting with optic pathway glioma with an early onset and an aggressive course.
Authors: Ganesh,
Gupta,
Sharma,
Bhuttan,
Issue Date: 23-Mar-2008
Citation: Ganesh S, Gupta A, Sharma M, Bhuttan S. A case of neurofibromatosis 1 presenting with optic pathway glioma with an early onset and an aggressive course. Indian Journal of Ophthalmology. 2008 March-April; 56(2): 161-162
Abstract: Optic pathway glioma associated with neurofibromatosis 1 has a classically indolent course. However, involvement of the optic radiations is relatively rare and is associated with a more aggressive course. A three-year-old girl presented with strabismus and loss of vision in the left eye with relative afferent pupillary defect and optic disc pallor. She had multiple cafiota au lait spots. Visually evoked potential was suggestive of an optic nerve conduction defect and magnetic resonance imaging of the brain was suggestive of an optic pathway glioma involving the optic nerves, the optic chiasma and the optic tracts. The optic radiations and the dendate nuclei had hamartomas. Optic nerve biopsy confirmed pilocytic astrocytoma. Radical radiotherapy under general anesthesia was subsequently given. This case report aims to highlight the involvement of the optic radiations and the unusually aggressive clinical course in this case.
URI: http://imsear.hellis.org/handle/123456789/71960
Appears in Collections:Indian Journal of Ophthalmology

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