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白塞氏病(Bechcets Disease)为临床难治疾病之一,其眼病变和全身合并症甚多,视力及生命予后均有较高的危险率。早在Behcet报告以前,地中海沿岸及中近东就曾多发此病。50～70年代中期日本有关本病的报告较多,占日本全部葡萄膜炎的7.6％。我国自1954年齐氏首次报告以来,临床病例报告亦屡见不鲜。但长期观察眼及全身各系统合并症及生命予后等报告尚未见到,笔者自1956至1982年间曾长期观察了3例患者,报导如下:
Bechcets disease is one of the most refractory diseases in clinical practice. There are many eye diseases and systemic complications, and high risk of vision and life. As early as the Behcet report, the disease was frequently reported on the Mediterranean coast and in the Near and Middle East. From 1950 to the mid-1970s, Japan reported more about this disease, accounting for 7.6% of all Japanese uveitis. Since the first report of Qi’s work in China in 1954, clinical case reports have not been uncommon. However, long-term observation of the ocular and systemic complications and life after the report has not been seen, the author from 1956 to 1982 had long-term observation of three patients, reported as follows: