Liou H H, Yip P K, Chang Y C, Liu H M
Department of Neurology, National Taiwan University Hospital, Taipei, ROC.
J Rheumatol. 1994 Dec;21(12):2380-4.
We describe a Chinese male patient with clinicopathologically definite Churg-Strauss syndrome. He had a clinical pattern of mononeuropathy multiplex and unusual optic neuritis, the latter probably being due to vasculitis related demyelination of the optic nerve. Magnetic resonance imaging of the brain revealed many clinically silent central nervous system lesions. He initially received steroid therapy, but an early cessation of treatment resulted in acute exacerbation. Later on, he was treated with combined prednisolone-cyclophosphamide therapy for 1 year. His ophthalmological and neurological symptoms responded well to such a regimen and disappeared within 6 months.
我们描述了一名患有临床病理确诊的变应性肉芽肿性血管炎综合征的中国男性患者。他具有多发性单神经病和不寻常的视神经炎的临床模式,后者可能是由于与视神经脱髓鞘相关的血管炎所致。脑部磁共振成像显示许多临床上无症状的中枢神经系统病变。他最初接受了类固醇治疗,但早期停药导致病情急性加重。后来,他接受了泼尼松龙-环磷酰胺联合治疗1年。他的眼科和神经症状对这种治疗方案反应良好,并在6个月内消失。