Fuchs spot

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

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.

References

↑ "Forster-Fuchs' Retinal Spot". patient.info. Retrieved 24 December 2012.

Symptoms and medical signs relating to the eye

Adnexa	lacrimal: Schirmer's test eyelid: Abadie's sign of exophthalmic goiter Boston's sign Dalrymple's sign Stellwag's sign

Globe	pupil: Argyll Robertson pupils Adie pupil Marcus Gunn pupil iris: Fleischer ring Kayser-Fleischer ring Brushfield spots Lisch nodule conjunctiva: Bitot's spots Arlt's line retina: Hollenhorst plaque Roth's spot Fuchs spot others: Alexander's law Hirschberg test Siegrist streaks Hudson–Stahli line

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Fuchs spot

Symptoms

See also

References