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后多形性角膜病变

Posterior polymorphous keratopathy.

作者信息

Liakos G M, Casey T A

出版信息

Br J Ophthalmol. 1978 Jan;62(1):39-45. doi: 10.1136/bjo.62.1.39.

Abstract

Seven cases with posterior polymorphous changes of the cornea are reported. After clinical and pathological examination of the above cases, as well as a short review of the literature, the following points are made: (1) Some cases are congenital, being either familial or sporadic, but others are acquired. (2) The term "posterior polymorphous keratopathy" covers all the variants of the condition and is preferred to the traditional "posterior polymorphous dystrophy". (3) The congenital type is a mild variant of the mesodermal dysplasia, whereas the acquired type follows local disease. (4) The condition can be static, but over 50% of cases are slowly progressive, calling for penetrating keratoplasty.

摘要

报告了7例角膜后多形性改变的病例。在对上述病例进行临床和病理检查以及对文献进行简要回顾后,得出以下几点:(1)一些病例是先天性的,可为家族性或散发性,但其他病例是后天获得性的。(2)“后多形性角膜病变”这一术语涵盖了该病的所有变体,比传统的“后多形性营养不良”更可取。(3)先天性类型是中胚层发育异常的一种轻度变体,而后天获得性类型继发于局部疾病。(4)该病可以是静止性的,但超过50%的病例呈缓慢进展,需要进行穿透性角膜移植术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3af/1043134/df6ad962a677/brjopthal00217-0049-a.jpg

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