韦格纳肉芽肿病的治疗。24年来111例患者的常规和分期调整治疗经验[j]。

L Briedigkeit, M Ulmer, E Rheinhold-Keller, U Göbel, R Natusch, W L Gross
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引用次数: 0

摘要

回顾性分析了1966年至1990年间111例韦格纳肉芽肿病(WG)患者的治疗和预后。确诊后平均观察时间为47(1 ~ 288)个月。在诊断时,37例患者仅出现局部症状,而74例患者出现全身性症状。区分了两种治疗方案:“常规”治疗,即每日应用环磷酰胺/泼尼松龙(FAUCI方案)或硫唑嘌呤/泼尼松龙或单独使用泼尼松龙,以及“分期适应”治疗,其特点是根据疾病的程度和活动性改变不同的治疗方法(例如环磷酰胺脉冲治疗,复方新诺明)。在接受分期适应治疗的患者中,复发发生率明显高于常规治疗的患者。另一方面,在常规治疗的患者中,致命的结果更为常见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Therapy of Wegener's granulomatosis. Experiences with conventional and stage-adjusted treatment in 111 patients over 24 years].

Treatment and outcome of 111 patients who fell ill with Wegener's granulomatosis (WG) between 1966 and 1990 were analysed retrospectively. The mean observation time after diagnosis had been 47 (1-288) months. At the time of diagnosis 37 patients suffered from locoregional symptoms only, whereas the disease was generalised in 74 patients. Two regimes of treatment were differentiated: "conventional" treatment, i.e. daily application of cyclophosphamide/prednisolone (FAUCI scheme) or azathioprine/prednisolone or prednisolone alone, and "stage-adapted" treatment, characterised by change of different treatments (e.g. cyclophosphamide pulse therapy, cotrimoxazole) according to the extent and activity of disease. In patients who received stage-adapted treatment, relapses occurred significantly more frequently than in conventionally treated patients. On the other hand, lethal outcome was much more frequent in conventionally treated patients.

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