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家族性渗出性玻璃体视网膜病变中的视网膜受累情况。

Retinal involvement in familial exudative vitreoretinopathy.

作者信息

Miyakubo H, Inohara N, Hashimoto K

出版信息

Ophthalmologica. 1982;185(3):125-35. doi: 10.1159/000309234.

Abstract

34 cases of familial exudative vitreoretinopathy were seen during a 40-month period ending April 1981. There were 30 cases from 11 families and 4 sporadic cases. The familial cases showed the mode of inheritance compatible with the autosomal-dominant inheritance. Ophthalmoscopy and super-wide panoramic fluorescein angiography revealed characteristic retinal vascular abnormalities in all cases, embracing supernumerous vascular branchings, arteriovenous shunt formation in the extreme periphery, generalized hyperpermeability of vessels and incomplete arteriovenous interdigitating pattern. Vitreoretinal adhesion was present in the peripheral temporal retina in all cases. An avascular zone wider than 1 disc diameter was noted in the majority of cases in the extreme temporal periphery. A V-shaped retinal degeneration was seen along the temporal meridian in 18 cases (48%). Retinal detachment was present in 19 eyes of 14 cases, and it was rhegmatogenous in 11 and traction-induced in 8 eyes. Retinal exudates and total posterior vitreous detachment was seen only occasionally.

摘要

在截至1981年4月的40个月期间,共发现34例家族性渗出性玻璃体视网膜病变。其中11个家族有30例,4例为散发病例。家族性病例的遗传方式符合常染色体显性遗传。检眼镜检查和超广角全景荧光血管造影显示,所有病例均有特征性的视网膜血管异常,包括血管分支过多、最周边部动静脉分流形成、血管普遍通透性增加以及动静脉交叉模式不完全。所有病例周边颞侧视网膜均存在玻璃体视网膜粘连。大多数病例在颞侧极周边部可见一个宽度超过1个视盘直径的无血管区。18例(48%)沿颞侧子午线可见V形视网膜变性。14例患者的19只眼发生视网膜脱离,其中11只为孔源性,8只为牵拉性。视网膜渗出和完全性玻璃体后脱离仅偶尔可见。

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