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Meesmann corneal dystrophy associated with epithelial basement membrane and posterior polymorphous corneal dystrophies.

机译:Meesmann角膜营养不良与上皮基底膜和后部多态性角膜营养不良有关。

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PURPOSE: To report a rare case of bilateral and symmetric Meesmann corneal dystrophy concurrent with bilateral epithelial basement membrane dystrophy and bilateral but asymmetric posterior polymorphous corneal dystrophy in a patient of Armenian origin. METHODS: Complete ophthalmologic examination was performed on a 6-year-old boy from Armenia who was diagnosed with bilateral symmetric Meesmann corneal dystrophy combined with bilateral epithelial basement membrane dystrophy and bilateral but asymmetric posterior polymorphous corneal dystrophy. This case was observed and treated for 24 years. RESULTS: On slit-lamp biomicroscopy, the patient showed bilateral multiple intraepithelial cystic lesions, bilateral irregularly shaped grayish-white opacities in the superficial corneal epithelium, and bilateral but asymmetric transparent vesicles surrounded by gray halos at the level of the Descemet membrane and the endothelium. CONCLUSIONS: This case is reported because of the unusual occurrence of Meesmann corneal dystrophy with other corneal dystrophies.
机译:目的:报道亚美尼亚籍患者的罕见的双侧和对称Meesmann角膜营养不良合并双侧上皮基底膜营养不良和双侧但不对称后部多形性角膜营养不良的病例。方法:对亚美尼亚的一名6岁男孩进行了完整的眼科检查,该男孩被诊断​​为双侧对称Meesmann角膜营养不良合并双侧上皮基底膜营养不良和双侧但不对称的后部多形性角膜营养不良。观察该病例并治疗24年。结果:在裂隙灯显微镜下,患者显示双侧多发性上皮内囊性病变,双侧不规则形状的灰白色混浊在浅表角膜上皮,双侧但不对称的透明囊泡在后桥膜和内皮水平处被灰色光晕包围。结论:该病例报道是由于梅斯曼角膜营养不良与其他角膜营养不良的异常发生。

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