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Fuchs异色性睫状体炎和眼部弓形体病各自都有非常明显的特征,根据其特点,临床上可以做出正确诊断。Fuchs异色性睫状体炎主要见于20—40岁的成年人,通常是单侧的,病情呈慢性过程,无疼痛或明显炎症。裂隙灯检查可见小的和中等大的白色KP,这些KP绝不融合,而是散布在纤维蛋白网上。前房反应轻微,细胞极少,闪光弱阳性。虹噗浅层萎缩、异色,有时有色素上皮萎缩。虹膜色素稀少者,在裂隙灯检查时,虹膜透光。
Fuchs heterochromocystitis and ocular toxoplasmosis each have very distinct characteristics, according to its characteristics, clinically correct diagnosis can be made. Fuchs heterochromatic ciliary body disease is mainly seen in adults 20 to 40 years old and is usually unilateral and has a chronic condition with no pain or marked inflammation. Slit lamp examination revealed small and medium white KP, these KP never fusion, but scattered in the fibrin network. Anterior chamber reaction mild, very few cells, flash weakly positive. Rainbow puffs shallow atrophy, discoloration, and sometimes pigment epithelial atrophy. Iris thinner, check the slit lamp, the iris light.