Fuchs spot

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The Fuchs spot or sometimes Forster-Fuchs' retinal spot is a degeneration of the macula in case of high myopia. It is named after the two persons who first described it: Ernst Fuchs, who described a pigmented lesion in 1901, and Forster, who described subretinal neovascularisation in 1862.[1] The size of the spots are proportionate to the severity of the pathological myopia.

An Optical coherence tomography (OCT) of the retina, showing a Fuchs spot.

Symptoms[edit]

First signs of a Fuchs spot are distorted sight of straight lines near the fovea, which some days later turn to the typical well-circumscribed patches after absorption of haemorrhage, and a pigmented scar remains. As in macular degeneration, central sight is affected. Atrophy leads to the loss of two or more lines of the Snellen chart.

See also[edit]

References[edit]

  1. ^ "Forster-Fuchs' Retinal Spot". patient.co.uk. Retrieved 24 December 2012.