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富克斯葡萄膜炎综合征患者眼部的脉络膜厚度

Choroidal Thickness in Eyes with Fuchs Uveitis Syndrome.

作者信息

Kardes Esra, Sezgin Akçay Betül Ilkay, Unlu Cihan, Ergin Ahmet

机构信息

a Umraniye Research and Training Hospital , Istanbul , Turkey.

出版信息

Ocul Immunol Inflamm. 2017 Apr;25(2):259-266. doi: 10.3109/09273948.2015.1115877. Epub 2016 Jan 14.

Abstract

PURPOSE

This study measured the macular thickness, peripapillary retinal nerve fiber layer (RNFL) thickness, subfoveal choroidal thickness (SFCT), and ganglion cell complex (GCC) thickness in eyes with Fuchs uveitis syndrome (FUS).

METHODS

In total, 25 patients with unilateral FUS were enrolled. The diagnosis of FUS was based on the presence of several of the following clinical features: absence of acute symptoms and ciliary injection; small to medium-sized and stellate keratic precipitates (KP) diffusely scattered on the entire corneal endothelium; chronic low-grade anterior chamber inflammation; iris stromal atrophy with or without heterochromia; lack of posterior synechiae; iris nodules; and vitreous cells and debris. Spectral domain optical coherence tomography (SD-OCT; RTVue-100 OCT) was used to obtain the measurements. The SFCT, RNFL thickness, macular retinal thickness, and GCC thickness of the eyes with FUS were measured and compared with those of the uninvolved fellow eyes. A paired samples t-test was used for statistical analyses. A value of p<0.05 was considered to be statistically significant for all analyses.

RESULTS

The mean age of the patients was 35.2 ± 4.8 years. Fifteen patients (60%) were male, and 10 (40%) were female. Small- to medium-sized stellate KPs and mild anterior chamber reactions were seen in all patients. Heterochromia was observed in 24% of the eyes, iris nodules in 36% of the eyes, lens opacity in 44% of the eyes, and vitreous cells and debris in 88% of the eyes. The mean SFCT was significantly thinner in eyes with FUS (296.47 ± 32.29 µm) than in the fellow eyes without FUS (324.47 ± 26.73 µm; p = 0.001). The mean average GCC thickness was found to be 101.09 ± 5.46 µm in eyes with FUS and 103.80 ± 6.65 µm in eyes without FUS (p = 0.023). There were no significant differences in the mean RNFL and macular thickness values.

CONCLUSIONS

We detected subfoveal choroidal thinning in eyes with FUS when compared with the uninvolved fellow eyes. In our opinion, thinning of the SFCT in FUS might be associated with autoimmune responses and chronic inflammatory processes.

摘要

目的

本研究测量了富克斯葡萄膜炎综合征(FUS)患者眼睛的黄斑厚度、视乳头周围视网膜神经纤维层(RNFL)厚度、黄斑中心凹下脉络膜厚度(SFCT)和神经节细胞复合体(GCC)厚度。

方法

共纳入25例单侧FUS患者。FUS的诊断基于以下几种临床特征:无急性症状和睫状充血;中小型星状角膜后沉着物(KP)弥漫性散在于整个角膜内皮;慢性低度前房炎症;虹膜基质萎缩伴或不伴异色症;无虹膜后粘连;虹膜结节;以及玻璃体细胞和碎屑。使用光谱域光学相干断层扫描(SD-OCT;RTVue-100 OCT)进行测量。测量FUS患者眼睛的SFCT、RNFL厚度、黄斑视网膜厚度和GCC厚度,并与未受累的对侧眼睛进行比较。采用配对样本t检验进行统计分析。所有分析中,p<0.05被认为具有统计学意义。

结果

患者的平均年龄为35.2±4.8岁。15例(60%)为男性,10例(40%)为女性。所有患者均可见中小型星状KP和轻度前房反应。24%的眼睛观察到异色症,36%的眼睛观察到虹膜结节,44%的眼睛观察到晶状体混浊,88%的眼睛观察到玻璃体细胞和碎屑。FUS患者眼睛的平均SFCT(296.47±32.29μm)明显比未患FUS的对侧眼睛(324.47±26.73μm;p = 0.001)薄。发现FUS患者眼睛的平均GCC厚度为101.09±5.46μm,未患FUS的眼睛为103.80±6.65μm(p = 0.023)。RNFL和黄斑厚度的平均值无显著差异。

结论

与未受累的对侧眼睛相比,我们检测到FUS患者眼睛的黄斑中心凹下脉络膜变薄。我们认为,FUS中SFCT变薄可能与自身免疫反应和慢性炎症过程有关。

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