Böhm M, Stark E, Fabel H
Dtsch Med Wochenschr. 1985 Feb 8;110(6):221-4. doi: 10.1055/s-2008-1068802.
In two female patients asthma, marked eosinophilia and symptoms of systemic vasculitis could be classified clinically or histologically as allergic angiitis and granulomatosis (Churg-Strauss syndrome). The course in one patient went back over 20 years, characterized by an asymptomatic interval of 16 years. It is to be assumed that the disease is more frequent than it is diagnosed. It has to be thought of when, in addition to asthma and eosinophilia, there is evidence of involvement of other organs.
在两名女性患者中，哮喘、明显的嗜酸性粒细胞增多以及系统性血管炎症状在临床或组织学上可归类为变应性血管炎和肉芽肿病（Churg-Strauss综合征）。其中一名患者的病程超过20年，其特征为有16年的无症状期。据推测，该疾病的实际发病率高于诊断率。当除哮喘和嗜酸性粒细胞增多外，还有其他器官受累的证据时，就必须考虑到该病。
