Weintraub M I
Am J Ophthalmol. 1977 Mar;83(3):355-7. doi: 10.1016/0002-9394(77)90733-4.
A 13-year-old girl suddenly experienced ataxia, bilateral external ophthalmoplegia, and areflexia. She was previously healthy but several family members had had a flu-like illness. Cerebrospinal fluid punctures demonstrated a persistent lymphocytosis and protein elevation. Clinical improvement occurred in several months. These findings represent a variant of Guillain-Barré-Strohl syndrome (infectious polyneuritis), a systemic illness rather than a primary ophthalmologic entity.
一名13岁女孩突然出现共济失调、双侧眼球外展麻痹和反射消失。她之前身体健康,但有几名家庭成员曾患类似流感的疾病。脑脊液穿刺显示淋巴细胞持续增多和蛋白质升高。数月后临床症状有所改善。这些表现代表了格林-巴利-施特罗尔综合征(感染性多发性神经炎)的一种变异型,这是一种全身性疾病而非原发性眼科疾病。