国际眼科纵览

• 综述 • 上一篇    下一篇

Cogan综合征

刘广森  高磊   

  1. 264000 青岛大学,青岛大学附属烟台毓璜顶医院(刘广森);261000青岛大学,潍坊眼科医院(高磊)
  • 收稿日期:2017-08-21 出版日期:2017-10-22 发布日期:2017-10-26
  • 通讯作者: 高磊,Email:gl6365@163.com

Cogan′s syndrome

LIU Guang-sen1, GAO Lei2.   

  1. 1.  Qingdao University,The affiliated Yantai Yuhuangding Hospital of Qingdao University,  Yantai 264000, China; 2.Weifang Ophthalmic Hospital, Qingdao University,  Weifang 261000, China
  • Received:2017-08-21 Online:2017-10-22 Published:2017-10-26
  • Contact: GAO Lei, Email: gl6365@163.com

摘要:

Cogan综合征是一种罕见的以非梅毒性角膜基质炎及听觉-前庭功能障碍为特点的综合征,病因尚不明确,可能为自身免疫性疾病。多在青年人发病,主要表现为非梅毒性角膜基质炎和听觉前庭功能障碍。分为典型性和非典型性。需与肉芽肿性多血管炎、类风湿性关节炎、系统性红斑狼疮等鉴别。治疗以糖皮质激素、免疫抑制剂为主。(国际眼科纵览, 2017,  41:   328-331)

Abstract:

Cogan′s syndrome (CS) is a rare disease,characterized by nonsyphilitic ocular keratitis and vestibuloauditory dysfunction.  The cause of the disease is unclear. It may be an autoimmune disease. The inicidence of the disease is mostly young people. The main manifestation are nonsyphilitic ocular keratitis and vestibulo auditory dysfunction. The CS is divided into typical and atypical. It needs to differentiate with granulomatosis with polyangiitis, rheumatoid arthritis, systemic lupus erythematosus. The treatment is mainly with glucocorticoids and immunosuppressive agents.(Int Rev Ophthalmol,  2017,  41:   328-331)