【MPO-ANCA相关性血管炎综合征患者的治疗效果及临床表现】。

Ryumachi. [Rheumatism] Pub Date : 2000-02-01
A Yoshida, A Takeda, M Fukuda, S Toda, K Morozumi
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引用次数: 0

摘要

我们研究了MPO(髓过氧化物酶)-ANCA(抗中性粒细胞胞浆抗体)相关血管炎综合征患者的临床表现、病程和治疗效果。我们分析了19例MPO-ANCA相关性血管炎的临床表现和资料。这些患者被诊断为临床症状(发热、关节痛、体重减轻等)、实验室数据(CRP高滴度、白细胞增多、血小板增多、MPO-ANCA高滴度)和坏死性血管炎的病理表现。患者男14例,女5例,年龄18 ~ 84岁(平均65岁),采用强的松龙和免疫抑制剂治疗,外加脉冲治疗和血浆置换治疗。7例在3个月内死亡。尸检显示这些病例死于肺炎、脑事件和胃出血。无免疫过度抑制致死亡病例。在存活病例中,这些治疗后MPO-ANCA水平迅速下降,这些抗体维持在较低水平(360至25 EU/l)。在死亡病例和存活病例的比较中,泼尼松龙的初始剂量(27 mg/天vs 56 mg/天)、双滤过血浆置换的比例(14% vs 42%)和免疫抑制治疗的比例(14% vs 83%)存在差异。MPO-ANCA的测定对MPO-ANCA相关性血管炎的诊断和治疗效果有重要意义。我们推荐积极治疗,包括强的松龙、免疫抑制剂和血浆置换治疗MPO-ANCA相关血管炎。我们相信积极的治疗可以提高MPO-ANCA相关性血管炎患者的生存率。
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[Therapeutic effect and clinical findings in patients with MPO-ANCA associated vasculitis syndrome].

We investigated to clarify the clinical findings, course and therapeutic effect in the patients with MPO (myeloperoxidase)-ANCA (anti-neutrophil cytoplasmic antibody) associated vasculitis syndrome. We analyzed clinical findings and data of 19 cases of MPO-ANCA associated vasculitis. These patients were diagnosed with clinical symptoms (fever, arthralgia, body weight loss, etc.), laboratory data (high titer of CRP, leukocytosis, thrombocytosis, and high titer of MPO-ANCA) and pathologic findings of necrotizing vasculitis. They were 14 male and 5 female aged 18 to 84 years (mean 65 years) and were treated with prednisolone and immunosuppressive agents, and additional therapy included pulse therapy and plasma exchange. Seven cases were dead within 3 months. Post-mortum examination showed that these cases died of pneumonitis, cerebral events and gastric bleeding. There was no mortal case induced by over-immunosuppression. In survival cases, the MPO-ANCA levels decreased rapidly after these therapies and these antibodies were maintained low levels (360 to 25 EU/l). Comparison of fatal cases and survival cases, there were difference in the initial dose of prednisolone (27 mg/day vs. 56 mg/day), the ratio of double filtration plasmapheresis (14% vs. 42%), and the ratio of immunosuppressive therapy (14% vs. 83%). The measurement of MPO-ANCA is useful makers of the diagnosis and effectiveness of the therapy in patients with MPO-ANCA associated vasculitis. We recommend the aggressive therapy, including prednisolone, immunosuppressive agents and plasma exchange for MPO-ANCA associated vasculitis. We believe that the aggressive therapy improve the survival rate of the patients with MPO-ANCA associated vasculitis.

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