血管免疫母细胞淋巴结病(Angio-i mmuno—blastic lymphadenopathydisease 简称 AILD),自1974年 Frizzeral、Lukes 等报告后引起国内外的广泛重视。AILD 的肺部表现比较特殊,本文报告2例。例1 男,42岁。因全身淋巴结肿大,伴同断性发烧近1年,1982年5月25日入院。患者于1981年7月始发现左侧颈部淋巴结肿大,不红,不痛,伴 Angio-i mmuno-blastic lymphadenopathydisease (AILD) has attracted wide attention both at home and abroad since its publication in 1974 by Frizzeral and Lukes. AILD lung performance is rather special, this article reports 2 cases. Example 1 male, 42 years old. Due to systemic lymphadenopathy, with the same break-off fever for nearly 1 years, May 25, 1982 admission. Patients in July 1981 began to find the left cervical lymph nodes, not red, no pain, with