Naumann G O, Schlötzer-Schrehardt U, Küchle M
Department of Ophthalmology, University of Erlangen-Nürnberg, Germany.
Ophthalmology. 1998 Jun;105(6):951-68. doi: 10.1016/S0161-6420(98)96020-1.
Renewed interest in pseudoexfoliation syndrome (PEX) may be attributed to an increased awareness of many clinical risks not only for open-angle glaucoma and its recent recognition as a generalized disorder. This review summarizes the range of intraocular and extraocular manifestations. Involvement of all tissues of the anterior segment of the eye results in a spectrum of intraocular complications that have management implication for all practicing ophthalmologists.
The study design was a review.
Clinical diagnosis depends on biomicroscopy, biocytology, and laser-tyndallometry. Laboratory research methods range from light and electron microscopy, to immunohistochemical and molecular biologic approaches.
Clinical-histopathologic correlations focus on the involvement of lens (PEX-phacopathy), zonular apparatus (zonulopathy), ciliary body (cyclopathy), iris (iridopathy), trabecular meshwork (trabeculopathy), and cornea (corneal endotheliopathy) leading to the following complications: (1) open-angle glaucoma as well as angle-closure glaucoma due to pupillary and ciliary block; (2) phacodonesis, lens dislocation, and increased incidence of vitreous loss in extracapsular cataract surgery caused by alterations of the zonular apparatus and its insertion into the ciliary body and lens; (3) blood-aqueous barrier breakdown (pseudouveitis), anterior chamber hypoxia, iris stromal hemorrhage, pigment epithelial melanin dispersion, poor or asymmetric pupillary dilatation, and formation of posterior synechiae due to involvement of all cell populations of the iris; and (4) early diffuse corneal endothelial decompensation explained by a damaged and numerically reduced endothelium.
In view of the multitude of clinical complications, PEX is of relevance to comprehensive ophthalmologists, including specialists in glaucoma, cataract, cornea, neuro-ophthalmology, and retina. Special attention to the risks associated with PEX is advised before, during, and after surgery.
对假性剥脱综合征(PEX)重新产生兴趣可能归因于人们不仅对开角型青光眼的诸多临床风险有了更高的认识,而且最近认识到它是一种全身性疾病。本综述总结了眼内和眼外表现的范围。眼前节所有组织的受累导致了一系列眼内并发症,这对所有执业眼科医生的治疗都有影响。
研究设计为综述。
临床诊断依赖于生物显微镜检查、生物细胞学检查和激光廷德尔ometry。实验室研究方法从光镜和电镜检查到免疫组织化学和分子生物学方法。
临床-组织病理学相关性集中在晶状体(PEX-晶状体病变)、悬韧带装置(悬韧带病变)、睫状体(睫状体病变)、虹膜(虹膜病变)、小梁网(小梁病变)和角膜(角膜内皮病变)的受累,导致以下并发症:(1)开角型青光眼以及由于瞳孔阻滞和睫状体阻滞引起的闭角型青光眼;(2)晶状体震颤、晶状体脱位,以及由于悬韧带装置及其插入睫状体和晶状体的改变导致的囊外白内障手术中玻璃体丢失发生率增加;(3)血-房水屏障破坏(假性葡萄膜炎)、前房缺氧、虹膜基质出血、色素上皮黑色素弥散、瞳孔扩张不良或不对称,以及由于虹膜所有细胞群受累导致的后粘连形成;(4)早期弥漫性角膜内皮失代偿,这是由受损且数量减少的内皮所解释的。
鉴于众多的临床并发症,PEX与包括青光眼、白内障、角膜、神经眼科和视网膜专家在内的综合眼科医生相关。建议在手术前、手术中和手术后特别关注与PEX相关的风险。