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[角膜内皮和后弹力层的继发性营养不良:组织学和超微结构研究(作者译)]

[Secondary dystrophies of corneal endothelium and Descemet's membrane: histological and ultrastructural study (author's transl)].

作者信息

Renard G, Dhermy P, Pouliquen Y

出版信息

J Fr Ophtalmol. 1981;4(11):721-39.

PMID:7035536
Abstract

Secondary alterations in Descemet's membrance were noted in corneal specimens from 20 patients undergoing transfixing keratoplasty, after examination by optical, and in some cases, by transmission or scanning electron microscopy. The most frequent anomaly, thickening of Descemet's membrance, was observed in cases of prolonged or recurrent corneal affections, particularly interstitial keratitis, advanced forms of keratoconus, cicatricial leukomas, and keratoconus. Thickening was due to juxtaposition, with a normal Descemet's membrance, of repair tissue made up of collagen interspersed with zones of cell necrosis and isolated fibrils. These different layers could be interpreted as successive deposits of reparative endothelial cells, the ultrastructural appearance of each layer being characteristic of the type of cell from which it was derived. In this way, the history of each cornea can be reconstituted, from the original normal endothelial cell to the final endothelial repair cells, passing through all the intermediary types of fibroblastic cells. This relationship between the cells which manufacture descemetic tissue and the structure of Descemet's membrance is particularly evident in Groenouw's macular dystrophy type II in which mucopolysaccarides are deposited. Descemetic verrucosities were observed in interstitial keratitis, of syphilitic origin or not, in one case of keratoconus, one case of buphthalmia, two cases of corneal leukoma, one case of vitreocorneal contact from aphakia, and in cases of Groenouw's type II dystrophy. The lesions are either isolated or spread across the posterior surface of the cornea. They differ from the verrucosities of primary cornea guttata by their irregular disposition, their frequent coalescence, the persistence of an endothelial regenerative process, their ultrastructural characteristics close to those of Hassal-Henlè's bodies, and more particularly by the association of a granular material with narrow and wide interval striated collagen. Various hypotheses are discussed which could provide an explanation why certain cells lay down Descemet's membrance in the form of tuberosities, and why these may present in alignments, but no satisfactory definite conclusion can be reached.

摘要

在对20例行穿透性角膜移植术患者的角膜标本进行光学检查,部分病例还进行透射或扫描电子显微镜检查后,发现后弹力层存在继发性改变。最常见的异常是后弹力层增厚,见于角膜疾病病程延长或复发的病例,尤其是间质性角膜炎、圆锥角膜晚期、瘢痕性角膜白斑和圆锥角膜。增厚是由于由胶原组成的修复组织与正常后弹力层并列,其中散布着细胞坏死区和孤立的原纤维。这些不同的层可被解释为修复性内皮细胞的连续沉积,每层的超微结构外观是其来源细胞类型的特征。通过这种方式,从原始的正常内皮细胞到最终的内皮修复细胞,经过所有中间类型的成纤维细胞,每个角膜的历史得以重构。制造后弹力层组织的细胞与后弹力层结构之间的这种关系在II型格罗诺夫黄斑营养不良中尤为明显,其中有粘多糖沉积。在间质性角膜炎(无论是否为梅毒起源)、1例圆锥角膜、1例牛眼、2例角膜白斑、1例无晶状体眼的玻璃体角膜接触病例以及II型格罗诺夫营养不良病例中观察到后弹力层疣状病变。病变可为孤立性或散布于角膜后表面。它们与原发性角膜小滴的疣状病变不同,其排列不规则、常融合、内皮再生过程持续存在、超微结构特征与哈萨尔-亨勒小体相似,更特别的是与颗粒物质和宽窄相间的条纹状胶原相关。讨论了各种假说,这些假说可以解释为什么某些细胞以后弹力层结节的形式沉积,以及为什么这些结节可能呈排列状,但无法得出令人满意的确切结论。

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