一例罕见的先天性单侧外层渗出性视网膜病变合并牵牛花综合征视盘异常病例。

Kremer I, Cohen S, Izhak R B, Ben-Sira I

Br J Ophthalmol. 1985 Jan;69(1):32-7. doi: 10.1136/bjo.69.1.32.

We present the case of a 13-year-old girl with a right congenital esotropia who at the age of 6 months presented an anomaly of the optic disc and retinal vessels in the same eye. In the following year she developed Coats's disease, rubeosis iridis, and neovascular glaucoma that led to enucleation. Pathological examination confirmed the clinical diagnosis.

我们报告一例13岁患有先天性右眼内斜视的女孩，她在6个月大时右眼出现视盘和视网膜血管异常。次年，她患上了科茨病、虹膜红变和新生血管性青光眼，最终导致眼球摘除。病理检查证实了临床诊断。