Veevaete F, van der Straeten M, de Vos M, Roels H
Scand J Respir Dis. 1978;59(6):287-96.
A 15-year-old boy died after a 3 years' illness; asthmatic bronchitis, recurrent heart failure and eosinophilia were the essential manifestations. The autopsy elicited a diagnosis of allergic granulomatous angiitis, because of angiitis with fibrinoid necrosis and granulomatous lesions in vascular and extravascular regions. The most important differential diagnostic aspects of this disease are discussed, especially the resemblances to Wegener's granulomatosis, hypersensitivity angiitis and polyarteritis nodosa.
一名15岁男孩患病3年后死亡;哮喘性支气管炎、反复心力衰竭和嗜酸性粒细胞增多是主要表现。尸检诊断为变应性肉芽肿性血管炎,因为血管和血管外区域存在伴有纤维素样坏死的血管炎和肉芽肿性病变。讨论了该疾病最重要的鉴别诊断要点,尤其是与韦格纳肉芽肿、超敏性血管炎和结节性多动脉炎的相似之处。