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眼部褐黄病。临床病理、组织化学及超微结构研究。

Ocular ochronosis. Clinicopathological, histochemical, and ultrastructural studies.

作者信息

Kampik A, Sani J N, Green W R

出版信息

Arch Ophthalmol. 1980 Aug;98(8):1441-7. doi: 10.1001/archopht.1980.01020040293017.

Abstract

Presented here are the clinical, histological, histochemical, and ultrastructural findings of an eye with notable ochronotic changes. Ochronotic pigment is seen by light microscopy as amber globules or fiber-like structures in the cornea, conjunctiva, and sclera combined with degenerated collagen. In the area of a previous injury the intense involvement of the cornea, which is usually not notably involved, indicates the role of preexisting degeneration for the development of clinically visible pigmentation. Although the ultrastructure of the ochronotic pigment is similar to melanin, the chemical behavior is different and, it seems, similar to elastin. Ultrastructurally, most of the pigment granules are extracellular, partly altering the collagen fibers and fibrocytes. The electron-microscopically observed four patterns of deposition are interpreted as stages in the development of ochronotic deposits, according to biochemical findings in the literature.

摘要

本文展示了一只出现明显褐黄病性改变的眼睛的临床、组织学、组织化学和超微结构检查结果。在光学显微镜下,褐黄病色素表现为角膜、结膜和巩膜中的琥珀色小球或纤维样结构,并伴有变性的胶原蛋白。在先前损伤的区域,通常未明显受累的角膜出现强烈病变,这表明先前存在的变性在临床上可见色素沉着的发展中所起的作用。尽管褐黄病色素的超微结构与黑色素相似,但其化学行为不同,似乎与弹性蛋白相似。超微结构上,大多数色素颗粒位于细胞外,部分改变了胶原纤维和成纤维细胞。根据文献中的生化研究结果,电镜观察到的四种色素沉积模式被解释为褐黄病沉积物发展的不同阶段。

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