Henriquez A S, Kenyon K R, Dohlman C H, Boruchoff S A, Forstot S L, Meyer R F, Hanninen L A
Surv Ophthalmol. 1984 Sep-Oct;29(2):139-47. doi: 10.1016/0039-6257(84)90171-1.
Based on their own study of nine corneas with clinically documented posterior polymorphous dystrophy and a review of the literature, the authors describe the morphologic features of this entity. Study by phase contrast light microscopy and transmission and scanning electron microscopy found that changes were primarily in the endothelium and consisted of endothelial cell degeneration and loss with focal fibroblastic and epithelial-like cell transformation. Secondary alterations of Descemet's membrane were seen; they consisted of abnormal lamination with deposition of abnormal collagen material, particularly in the posterior collagen layer, and formation of guttate excrescences and pits.
基于他们自身对9只临床诊断为后多形性营养不良的角膜的研究以及对文献的回顾,作者描述了该疾病的形态学特征。通过相差显微镜、透射电子显微镜和扫描电子显微镜研究发现,变化主要发生在内皮细胞层,表现为内皮细胞变性和丢失,伴有局灶性成纤维细胞和上皮样细胞转化。观察到Descemet膜的继发性改变;包括异常分层,伴有异常胶原物质沉积,特别是在后胶原层,以及形成滴状赘生物和凹坑。