Prolonged follow-up of 36 children with optic glioma confirms that the tumour is congenital, non-neoplastic, and self-limiting, and has a good prognosis for life. Visual impairment, present at the time of diagnosis, does not change appreciably thereafter. Excision of such a tumour should be undertaken only to control proptosis in a blind eye. Life cannot be prolonged by irradiation or transcranial procedures on the tumour.
CITATION STYLE
Hoyt, W. F., & Baghdassarian, S. A. (1969). Optic glioma of childhood: Natural history and rationale for conservative management. British Journal of Ophthalmology, 53(12), 793–798. https://doi.org/10.1136/bjo.53.12.793
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