Kempf H G
CHU de Tübingen, Chef de Service.
Rev Laryngol Otol Rhinol (Bord). 1990;111(1):67-9.
In the last 21 years, 22 histologically proven cases of Wegener's granulomatosis (WG) were observed and treated. In 19 patients WG appeared primarily in the ENT-area. Ten patients had middle ear involvement. Whereas, in 9 cases the inner ear was affected too. Before introduction of immunosuppressive therapy the patients (n = 8) died averagely after 5.6 months after onset of the first symptoms. Under therapy with cyclophosphamide and prednisone total remission of WG can be reached for long times (n = 14, 3.2 years of follow up). In 14 cases serologically anti-cytoplasmatic antibodies against neutrophil granulocytes were determined in high activity stage of WG. In combination with the clinical and histological findings the determination of these antibodies gives the possibility to solve difficulties in differential diagnosis of WG.
在过去的21年里,观察并治疗了22例经组织学证实的韦格纳肉芽肿病(WG)病例。19例患者的WG主要出现在耳鼻喉区域。10例患者中耳受累。此外,9例患者内耳也受到影响。在引入免疫抑制治疗之前,8例患者在出现首发症状后平均5.6个月死亡。使用环磷酰胺和泼尼松治疗后,WG可长期完全缓解(14例,随访3.2年)。14例患者在WG的高活动期检测到血清抗中性粒细胞胞浆抗体。结合临床和组织学检查结果,这些抗体的检测有助于解决WG鉴别诊断中的难题。