论文部分内容阅读
变态反应性肉芽肿性脉管炎(AGA)是1951年Churg及Strauss将支气管哮喘、嗜酸性细胞增多、全身坏死性脉管炎作为三联综合征,从古典的结节性多动脉炎(PN)分出的一种独立疾病。在日本由厚美等(1964年)首次报告,此后有零星报道。进入80年代后,引起人们的关注,已有许多报告。作者作为日本厚生省系统性损害调查研究班的一员,曾提出AGA的诊断指标(1981年),在日本进行了第1次(1982年)、第2次(1983年)AGA调查,提出了日本AGA病例的临床特点。此后,有关AGA的病例报道增多,于1986年12月进行第3次调查。调查结果,弄清了,日本AGA的临床特点,在详细报告的同时,根据调查结果拟订了AGA的临床诊断标准。
Allergic granulomatous vasculitis (AGA) was established in 1951 by Churg and Strauss as bronchial asthma, eosinophilia, and systemic necrotizing vasculitis as triplet syndromes from classic nodosa polyarteritis (PN) A separate disease. It was first reported in Japan by Hou Mei et al. (1964) and then sporadically reported. Since the 1980s, there have been many reports that have drawn people’s attention. The author, as a member of the Japanese Ministry of Health and Welfare Systemic Damage Investigation, proposed the diagnostic criteria for AGA (1981), the first (1982) and the second (1983) AGA surveys in Japan, and proposed that Japan Clinical features of AGA cases. Since then, there have been more cases of AGA, and the third survey was conducted in December 1986. The results of the investigation revealed that the clinical features of the Japanese AGA were based on detailed findings and the clinical diagnostic criteria for AGA were developed based on the findings.