Peeters G J, Cremers C W, Pinckers A J, Hoefnagels W H
Ann Otol Rhinol Laryngol. 1986 Mar-Apr;95(2 Pt 1):173-5. doi: 10.1177/000348948609500213.
A 22-year-old woman is described with gastrointestinal complaints, sclerokeratitis, and a bilateral progressive hearing loss. The clinical picture, the outcome of lymphocyte stimulation tests against S antigen (retina soluble antigen), outer rod segment, and scleroprotein, and the successful administration of corticosteroids after a partial spontaneous hearing improvement, are suggestive of an autoimmune disease.
一名22岁女性出现胃肠道不适、巩膜角膜炎和双侧进行性听力丧失。临床表现、针对S抗原(视网膜可溶性抗原)、外节杆段和硬蛋白的淋巴细胞刺激试验结果,以及在听力部分自发改善后成功使用皮质类固醇治疗,提示为自身免疫性疾病。