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[施奈德原发性遗传性结晶性角膜营养不良。组织病理学与超微结构(作者译)]

[Primary hereditary cristalline corneal dystrophy of Schnyder. Histopathology and ultrastructure (author's transl)].

作者信息

Pfannkuch F

出版信息

Klin Monbl Augenheilkd. 1978 Sep;173(3):355-8.

PMID:312360
Abstract

The present study consists of light- and electron-microscopic examination of excised cornea in a case of lipid keratopathy (Schnyder) in which a perforating keratoplasty was performed. It demonstrates the deposition of cristalline and non-cristalline substances in the corneal epithelium as well as the anterior half of the corneal stroma. Histiocytic elements infiltrate the subepithelial connective tissue. Bowman's membrane is conspicuously almost totally missing. The paper concludes with a discussion of the above findings.

摘要

本研究包括对一例施行了穿透性角膜移植术的脂质角膜病变(施奈德病)患者切除角膜的光镜和电镜检查。它显示了晶体和非晶体物质在角膜上皮以及角膜基质前半部分的沉积。组织细胞成分浸润上皮下结缔组织。鲍曼膜明显几乎完全缺失。本文最后对上述发现进行了讨论。

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