Behcet 氏病多见于东地中海盆地,但世界各地均有报告。本文报告28例1938～1963年地中海东岸黎巴嫩等国的患者。男性26例,女性2例,年龄11～37岁,其中2例为见弟二人均患此病。病程:此病的特点为慢性复发性,平均每年发作4～5次,随疾病的发展而发作次数逐渐减少。一例已患病26年,现虽失明,每年仍复发1～2次。此病最终几乎总是失明。当此病达严重阶段,于少数病例产生神经系统并发症,此时生命的预后常不佳。开始症状:此病开始偶有周身乏力,低烧。常有多次急性扁桃腺炎病史,下肢游走性关节痛或结节性 Behcet’s disease is more common in the Eastern Mediterranean basin, but reports are available from all over the world. This article reports 28 patients from 1938 to 1963 in countries such as Lebanon on the eastern Mediterranean coast. There were 26 males and 2 females, aged from 11 to 37 years old, two of whom were affected by the disease. Course of disease: The disease is characterized by chronic recurrent, an average of 4 to 5 episodes per year, with the development of the disease and the number of seizures gradually reduced. One case has been ill for 26 years, although it is blind, recurrence still occurs once or twice a year. The disease eventually ends up being almost always blind. When the disease reaches a serious stage, nervous system complications occur in a few cases, and the prognosis of life is often poor. Start Symptoms: The disease starts with occasional whole body fatigue, fever. Often many times the history of acute tonsillitis, lower extremity migratory joint pain or nodularity