Bruneton J N, Dilhuydy M H, de Mascarel A, Le Treut A
Poumon Coeur. 1979;35(1):5-9.
From 20 observations, the authors worked out the frequency and the radiological picture of chest localizations of angio-immunoblastic lymphadenitis (A.I.L.). There are 2 kinds of pulmonary involvement: --a specific one by interstitial immunoblastic infiltration (20 to 45% of cases) and showing on X ray a reticulomicronodular interstitial syndrome; --a secondary infection (33% of cases) often the cause of death. Pleural involvement is unfrequent (11% to 25% of cases) and its onset late. Mediastinal lymph-node involvement is found in 37 to 50% of cases. It is usually discovered straight away.
通过20例观察，作者得出血管免疫母细胞性淋巴结炎（A.I.L.）胸部定位的频率和放射学表现。肺部受累有两种情况：——一种是特异性的，由间质免疫母细胞浸润引起（占病例的20%至45%），X线表现为网状小结节间质综合征；——继发性感染（占病例的33%），常为死亡原因。胸膜受累不常见（占病例的11%至25%），且发病较晚。纵隔淋巴结受累见于37%至50%的病例，通常可立即发现。
