Goulart R A, Mark E J, Rosen S
Department of Pathology, Harvard Medical School, Beth Israel Hospital 02215.
Am J Surg Pathol. 1995 Feb;19(2):145-53. doi: 10.1097/00000478-199502000-00003.
Wegener's granulomatosis appeared as localized or infiltrative tumefactions in six patients. The tissue swellings affected the retroperitoneum, mediastinum (two), breast, retroorbital tissue (two), and gingiva. There was extensive fibroblastic proliferation in each case with a predominantly granulocytic inflammatory component, microabscess formation, and collagen necrobiosis. In one of the mediastinal lesions and in the gingiva, there was a granulomatous component as well. In the breast were scattered multinucleated histiocytes. Necrotizing vasculitis was absent or limited in all cases. All patients responded dramatically to cyclophosphamide and/or prednisone after the diagnosis was established. These observations indicate a role for tissue destruction in Wegener's granulomatosis mediated by granulocytes without a vasculitic component.
韦格纳肉芽肿病在6例患者中表现为局限性或浸润性肿块。组织肿胀累及腹膜后、纵隔(2例)、乳房、眶后组织(2例)和牙龈。每例均有广泛的成纤维细胞增生,主要为粒细胞性炎症成分、微脓肿形成和胶原坏死。在1例纵隔病变和牙龈病变中也有肉芽肿成分。乳房中有散在的多核组织细胞。所有病例均无坏死性血管炎或仅有局限性坏死性血管炎。所有患者确诊后对环磷酰胺和/或泼尼松反应显著。这些观察结果表明,在无血管炎成分的情况下,粒细胞介导的组织破坏在韦格纳肉芽肿病中起作用。