Abstract
A case of choroidal osteoma presenting in a 22-year-old girl is reported. The tumour, unilateral and in a juxtapapillary site, appeared markedly elevated on the retinal plane, not flat or slightly elevated as in previous reports. Visual acuity was not affected, and there was a complete absence of subjective symptoms. Echography, fluorangiography, computerised tomography, and visual field tests were performed. Echography is the best method for identifying and differentiating this lesion from a malignant tumour.
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CITATION STYLE
Cennamo, G., Jaccarino, G., De Crecchio, G., & Liguori, G. (1990). Choroidal osteoma (osseous choristoma): An atypical case. British Journal of Ophthalmology, 74(11), 700–701. https://doi.org/10.1136/bjo.74.11.700
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