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前部增殖性玻璃体视网膜病变。临床病理、光学显微镜及超微结构研究结果

Anterior proliferative vitreoretinopathy. Clinicopathologic, light microscopic, and ultrastructural findings.

作者信息

Elner S G, Elner V M, Díaz-Rohena R, Freeman H M, Tolentino F I, Albert D M

机构信息

Eye Research Institute of the Retina Foundation, Boston.

出版信息

Ophthalmology. 1988 Oct;95(10):1349-57. doi: 10.1016/s0161-6420(88)33003-4.

Abstract

Proliferative vitreoretinopathy (PVR) involving the posterior and equatorial retina is an established clinicopathologic entity. Clinically, a similar process, anterior PVR (APVR), results in anterior dragging of the peripheral retina by membranes which connect to the ciliary body or iris and cause circumferentially and radially fixed retinal folds. The pathology of APVR, however, has not been reported. The authors describe pathologic findings in 28 cases of APVR and ultrastructural pathologic findings in 6 surgical APVR specimens. Anterior PVR was frequently associated with retinal detachment (RD) repair (96%) and trauma (38%). Residual vitreous at the vitreous base virtually always provided a scaffold for membranes containing proliferating cells and deposited extracellular matrix. Major components of APVR membranes were fibrovascular tissue (71%), pigment epithelial cells (43%), fibrous and corneal stromal ingrowth (32%), and glial proliferation (18%). Because of its anterior location, APVR membranes also incorporated ciliary epithelium and corneal endothelium. Contraction of APVR membranes caused anterior retinal displacement and detachment in anatomic configurations corresponding to narrow and wide peripheral troughs. The authors' findings indicate that APVR is a distinctive clinicopathologic entity which may complicate rhegmatogenous RD and its repair.

摘要

累及后部和赤道部视网膜的增殖性玻璃体视网膜病变(PVR)是一种已明确的临床病理实体。临床上,类似的过程,即前部PVR(APVR),会导致周边视网膜被连接至睫状体或虹膜的膜向前牵拉,从而引起沿圆周和径向固定的视网膜皱褶。然而,APVR的病理学尚未见报道。作者描述了28例APVR的病理发现以及6例手术切除的APVR标本的超微结构病理发现。前部PVR常与视网膜脱离(RD)修复(96%)和外伤(38%)相关。玻璃体基底部的残留玻璃体几乎总是为含有增殖细胞和沉积细胞外基质的膜提供支架。APVR膜的主要成分是纤维血管组织(71%)、色素上皮细胞(43%)、纤维和角膜基质内生长(32%)以及神经胶质增生(18%)。由于其前部位置,APVR膜还包含睫状体上皮和角膜内皮。APVR膜的收缩导致视网膜向前移位并脱离,其解剖形态与周边窄槽和宽槽相对应。作者的发现表明,APVR是一种独特的临床病理实体,可使孔源性RD及其修复过程复杂化。

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