Brooks A M, Grant G, Gillies W E
Royal Victorian Eye and Ear Hospital, East Melbourne, Australia.
Aust N Z J Ophthalmol. 1987 Nov;15(4):283-9. doi: 10.1111/j.1442-9071.1987.tb00085.x.
We have demonstrated the reversibility of corneal endothelial changes which accompany superficial keratopathy (superficial punctate keratitis, exposure keratopathy, chemical keratopathy and keratoconjunctivitis sicca), stromal keratitis and anterior uveitis (predominantly iridocyclitis). These changes include small subendothelial dark areas equal to or less than one cell in diameter and larger subendothelial dark areas up to two to four cells in diameter. These dark areas are similar but form two groups. The smaller ones may be due to oedema, some developing into larger dark areas, but it is also possible that smaller dark areas represent inflammatory cells or even local destruction of endothelial cells. The larger dark areas elevate the overlying endothelium. Either may be very numerous. They may be present together or separately. They become much less numerous and disappear with resolution or suppression of the acute keratitis or uveitis. The relief mode of corneal specular microscopy was used to distinguish these dark areas from other inflammatory and degenerative changes (such as fine inflammatory deposits, larger keratic precipitates, pigment deposits and guttatae at the level of the corneal endothelium).
我们已经证实了与浅层角膜病变(浅层点状角膜炎、暴露性角膜炎、化学性角膜炎和干燥性角结膜炎)、基质性角膜炎和前葡萄膜炎(主要是虹膜睫状体炎)相关的角膜内皮变化是可逆的。这些变化包括直径等于或小于一个细胞的小的内皮下暗区以及直径达两到四个细胞的较大的内皮下暗区。这些暗区相似但形成两组。较小的暗区可能是由于水肿,有些会发展成较大的暗区,但较小的暗区也可能代表炎症细胞甚至内皮细胞的局部破坏。较大的暗区会使上方的内皮细胞隆起。两者都可能非常多。它们可能同时出现或单独出现。随着急性角膜炎或葡萄膜炎的消退或得到控制,它们的数量会大大减少并消失。使用角膜内皮显微镜的缓解模式将这些暗区与其他炎症和退行性变化(如细小的炎症沉积物、较大的角膜后沉着物、色素沉着和角膜内皮水平的角膜小滴)区分开来。