Cogan syndrome: An autoimmune eye and ear disease with systemic manifestations

被引:5
|
作者
Bhandari, Gurbir Singh [1 ]
Duggal, Lalit [2 ]
Jain, Neeraj [2 ]
Patel, Jeet [2 ]
机构
[1] Adesh Inst Med Sci & Res, Dept Rheumatol, Bathinda, Punjab, India
[2] Sir Ganga Ram Hosp, Dept Rheumatol & Clin Immunol, New Delhi, India
来源
NATIONAL MEDICAL JOURNAL OF INDIA | 2019年 / 32卷 / 06期
关键词
D O I
10.4103/0970-258X.303611
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cogan syndrome (CS) is a rare vasculitis seen primarily in young adults. It predominantly affects eyes, ears and the heart with characteristic findings of interstitial keratitis, sensorineural hearing loss and vestibular dysfunction. A high index of suspicion is required to diagnose this rare disorder. It is one of the few vasculitis which can involve vessels of all sizes: small, medium and large. Coexistence of inflammatory bowel disease (IBD) in Cogan syndrome has been described in the literature. Immunosuppressive agents such as corticosteroids with or without steroid sparing agents are the standard of care. Early diagnosis and treatment are the cornerstone of treatment to prevent permanent damage to the ears and eyes. We describe a patient with Cogan syndrome with large vessel vasculitis and IBD. Our patient was treated with glucocorticoids and methotrexate.
引用
收藏
页码:349 / 351
页数:3
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