Zhivov A, Stachs O, Kraak R, Guthoff R
Augenklinik, Universität Rostock.
Klin Monbl Augenheilkd. 2008 Jan;225(1):86-90. doi: 10.1055/s-2008-1027130.
Corneal ulcers can be observed occasionally due to infections, wearing contact lenses or in dry eyes. Confocal microscopy represents a new tool for the differential diagnostic work-up of pathological processes and provides the possibility for dynamic healing control.
We report on the corneal morphological changes caused by corneal ulcers of varying aetiologies. Morphological changes and pathological processes in infiltrates as well as in ulcus corneae can be investigated by means of the confocal in vivo microscopy based on the confocal laser scanning microscope model Heidelberg Retina Tomograph II with the Rostock cornea module.
Corneal infiltrates are characterised by inflammatory cell infiltration without other morphological changes. An advanced process like corneal ulcer is characterised by not only the tissue defects but also by oedematous structures of the entire cornea resulting in an increase in corneal thickness, increased cell density of leukocytes and of Langerhans cells. The scar tissue formation as well as epithelium regeneration are documented during the follow-up. Confocal detection of pathogens (acanthamoeba, fungus, etc.) was performed.
The confocal microscopic data about micromorphological changes could be useful in the evaluation of defect geometry and healing processes of the cornea. Differential diagnostic distinction between bacterial, fungal or acanthamoeba genesis is possible.
角膜溃疡偶尔可因感染、佩戴隐形眼镜或干眼症而出现。共聚焦显微镜是用于病理过程鉴别诊断检查的一种新工具,并为动态愈合监测提供了可能。
我们报告了不同病因引起的角膜溃疡所导致的角膜形态学变化。基于带有罗斯托克角膜模块的海德堡视网膜断层扫描仪II型共聚焦激光扫描显微镜的共聚焦活体显微镜,可研究浸润灶以及角膜溃疡中的形态学变化和病理过程。
角膜浸润的特征是炎性细胞浸润,无其他形态学改变。像角膜溃疡这样的进展期病变不仅以组织缺损为特征,还以整个角膜的水肿结构为特征,导致角膜厚度增加、白细胞和朗格汉斯细胞的细胞密度增加。随访期间记录了瘢痕组织形成以及上皮再生情况。对病原体(棘阿米巴、真菌等)进行了共聚焦检测。
关于微观形态学变化的共聚焦显微镜数据可能有助于评估角膜缺损的几何形状和愈合过程。细菌、真菌或棘阿米巴病因的鉴别诊断是可能的。