Scleral Disease
Melanosis oculi (ocular melanocytosis) is a congenital blue nevus of the episclera and sclera associated with increased pigmentation of the uveal tract.

Multiple gray pathces are seen in the sclera and episclera, and the ipsilateral iris and fundus are darker than those of the unaffected eye.

Melanosis oculi with melanosis of the ipsilateral eyelid skin is referred to as oculodermal melanocytosis (nevus of Ota).

The most serious complication of the oculodermal melanocytosis is malignant transformation, although this is rare and seems to occur only in white patients. Malignant transformation in the skin, conjunctiva, orbit, and meninges is possible but rare.

Previous

Next


Scleritis | Episcleritis | Scleromalacia Perforans | Congenital Melanosis Oculi


Eye Lid | Lacrimal System Disorders | Scleral Disease


Home