Hui A N, Ehresmann G R, Quismorio F P, Boylen C T, Mayberg H, Koss M N
Chest. 1981 Dec;80(6):753-6. doi: 10.1378/chest.80.6.753.
We report a case of classic Wegener's granulomatosis. Direct immunofluorescent study showed finely granular deposits of IgG and IgM in some of the alveolar walls, and of IgM in the maxillary sinus arteries. Electron-microscopic study of the lung and maxillary sinus showed intravascular fibrin, but failed to demonstrate electron-dense deposits in the blood vessel walls. Our patient also had circulating cryoglobulins, consisting of IgG, IgM, Clq, and C3, and evidence of circulating immune complexes as demonstrated by the Clq-binding test. These findings suggest that circulating immune complexes may play an important role in the pathogenesis of the respiratory lesions of Wegener's granulomatosis.
我们报告一例典型的韦格纳肉芽肿病。直接免疫荧光研究显示,部分肺泡壁有IgG和IgM的细颗粒状沉积,上颌窦动脉有IgM沉积。对肺和上颌窦的电子显微镜研究显示血管内有纤维蛋白,但未在血管壁发现电子致密沉积物。我们的患者还存在循环冷球蛋白,由IgG、IgM、Clq和C3组成,Clq结合试验证明有循环免疫复合物的证据。这些发现提示,循环免疫复合物可能在韦格纳肉芽肿病肺部病变的发病机制中起重要作用。