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白塞氏病为一病因未明的综合征。主要临床特征为复发性虹膜睫状体炎,口腔和生殖器溃疡。大量报告说明,此征还可累及皮肤、关节、心血管、消化各系统。1941年knapp首次报道合并神经症状的本综合征称神经白塞氏病。国外神经白塞氏病的发病率约为白塞氏病的10～25％(11、12)。我国自1957年齐氏首次报告2例,至1979年9月已有512例,其中神经白塞氏病共16例(2～10)。我院历年收治白塞氏病19例,其中有神经损害者3例,现报告如下。
Behcet’s disease is a syndrome of unknown etiology. The main clinical features of recurrent iridocyclitis, oral and genital ulcers. A large number of reports show that this sign can also affect the skin, joints, cardiovascular, digestive system. 1941 knapp first reported this syndrome with neurological symptoms called neurobeitosis. The incidence of foreign neuronal Behcet’s disease is about 10 to 25% of Behcet’s disease (11,12). Since 1957, Qi’s first report of 2 cases in China, to 1979 September has 512 cases, of which a total of 16 cases of neurocissel disease (2 to 10). 19 cases of Behcet’s disease were treated in our hospital over the years, including 3 cases of nerve damage, are as follows.