Abstract
Neuroretinitis was first described in 1916 by the German ophthalmologist Theodor Karl Gustav von Leber [1], who described a condition of unilateral vision loss associated with optic disc edema and a stellate pattern of macular exudates. Believing this represented retinal dysfunction, Leber characterized the condition as an “idiopathic stellate maculopathy.” Since then, the condition has gone by several names, including Leber’s stellate maculopathy, acute macular neuroretinopathy, Leber’s idiopathic stellate neuroretinitis, and Leber’s stellate optic neuritis. Gass and others recognized that disc swelling preceded the formation of the macular exudates and that the retinal vessels were angiographically quiescent. These observations lead Gass and others to suggest that the exudates arise from the optic disc and not the retina. Gass hypothesized further that the process resulted from an inflammatory insult to the optic nerve and renamed the syndrome “neuroretinitis”. Neuroretinitis is relatively rare, described in less than 1 % of all patients in large uveitis surveys. A number of infectious and noninfectious causes of neuroretinitis have been identified (Tables 47.1a and 47.1b).
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London, N.J.S., Cunningham, E.T. (2016). Neuroretinitis. In: Zierhut, M., Pavesio, C., Ohno, S., Orefice, F., Rao, N. (eds) Intraocular Inflammation. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-75387-2_47
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