Arsava E M, Uluç K, Kansu T, Dogulu C F, Soylemezoglu F, Selekler K
Department of Neurology, Hacettepe University Hospitals, Ankara, Turkey.
J Neuroophthalmol. 2001 Mar;21(1):34-6. doi: 10.1097/00041327-200103000-00010.
A 53-year-old woman with symptoms of hypopituitarism and ophthalmoplegia was diagnosed as having idiopathic granulomatous hypophysitis and later developed bilateral optic neuritis. She responded well to steroid treatment. Granulomatous hypophysitis is a rare entity, and this is the first reported case associated with optic neuritis.
一名53岁有垂体功能减退和眼肌麻痹症状的女性被诊断为特发性肉芽肿性垂体炎，随后发展为双侧视神经炎。她对类固醇治疗反应良好。肉芽肿性垂体炎是一种罕见疾病，这是首例报告的与视神经炎相关的病例。
