神经Behcet病病例常表现为以脑干、脊髓为主的脑脊髓炎征象。脑于脑炎临床、病理与神经Behcet病 很相似,故临床上对缺乏皮肤、粘膜及眼症状的Behcet病鉴别起来有一定的难度。 本文作者报告5例神经Behcet症候群均系男性,其中2例无皮肤粘膜症状。发病年龄20～40岁,病程1～10年,临床以反复进行性不完全缓解,再燃经过为 Neurological Behcet disease often manifested as brainstem, spinal cord-based signs of encephalomyelitis. Brain in encephalitis clinical, pathological and neurological Behcet disease is very similar, so the clinical lack of skin, mucous membranes and ocular symptoms of Behcet disease identification there is a certain degree of difficulty. The authors report that all five neurobending Behcet’s syndromes were male, with 2 of them having no skin mucosal symptoms. Age 20 to 40 years of age, duration of 1 to 10 years, the clinical progressively incomplete remission, and then after the burn