山东大学耳鼻喉眼学报 ›› 2018, Vol. 32 ›› Issue (2): 99-102.doi: 10.6040/j.issn.1673-3770.0.2017.354
谢洪彬,杨美娜,陈青山,刘旭阳,樊宁
XIE Hongbin, YANG Meina, CHEN Qingshan, LIU Xuyang, FAN Ning
摘要: 目的 免疫球蛋白G4-相关性疾病(IgG4-RD)是近年来逐渐被认识的一类相对少见的、与淋巴细胞密切相关的系统性疾病,IgG4-RD可累及一个或多个器官,当累及眼部组织时,则称为IgG4相关性眼病(IgG4-ROD)。本文分析IgG4相关性眼病伴继发性青光眼病例,探讨其治疗方法。 方法 分析IgG4相关性眼病伴继发性青光眼患者临床表现,综合组织活检、影像学检查、患者对激素治疗的应答以及长期观察等因素。 结果 血清IgG4水平升高是考虑该病最重要的血清学特征,具有较高的诊断价值,但特异性不高。本病需长期使用糖皮质激素治疗,多数患者对激素治疗应答良好,临床症状和器官功能均可得到改善,IgG4水平也有所降低。 结论 IgG4-ROD导致继发性青光眼是其并发症之一,其手术方式的选择和术后远期效果缺乏临床经验。该病变本身及长期使用激素所引起的眼部并发症值得关注。
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