Raines M F, Duvall-Young J, Short C D
Manchester Royal Eye Hospital.
Br J Ophthalmol. 1989 Nov;73(11):907-10. doi: 10.1136/bjo.73.11.907.
We have described a complex abnormality of retinal pigment epithelium, Bruch's membrane, and choriocapillaris in mesangiocapillary glomerulonephritis (MCGN) type II. Patients with MCGN type II were examined by vitreous fluorophotometry which reveals that there is a breakdown of the blood retinal barrier (BRB) in those patients with the typical fundus lesions. The function of this barrier was calculated as a penetration ratio and was statistically greater in these patients when compared with a group of (a) normal persons, (b) patients with drusen, and (c) patients with other forms of glomerulonephritis.
我们已经描述了II型系膜毛细血管性肾小球肾炎(MCGN)中视网膜色素上皮、布鲁赫膜和脉络膜毛细血管的复杂异常。通过玻璃体荧光光度法对II型MCGN患者进行检查,结果显示,那些具有典型眼底病变的患者存在血视网膜屏障(BRB)破坏。该屏障的功能以渗透比计算,与(a)正常人群、(b)有玻璃膜疣的患者和(c)其他形式肾小球肾炎患者组相比,这些患者的渗透比在统计学上更高。