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[以多发性肌炎为表现的变应性肉芽肿性血管炎:一例报告]

[Churg-Strauss syndrome presenting as polymyositis: report of a case].

作者信息

Lazzarin P, Presotto F, Polo A

机构信息

Ambulatorio di Reumatologia, Ospedale di Este, Padova, Italia.

出版信息

Reumatismo. 2009 Apr-Jun;61(2):140-4. doi: 10.4081/reumatismo.2009.140.

Abstract

We reported the case of a male patient with Churg-Strauss syndrome (CSS) heralding as symptoms typical of polymiositis. During high-dose cortisone therapy (1.5 mg/kg/day), he developed a severe multiplex mononeuritis, poorly responsive to immunoglobulins and methotrexate administration. After 6 months he developed a partial deficiency of the right sciatic popliteus and the radial nerves. Sural nerve biopsy showed a characteristic necrotizing vasculitis of the epineural vessels with granulocyte and eosinophil infiltrates. In the course of CSS, peripheral nervous system involvement is frequent and can lead to disability. For this reason, it must be promptly recognized and properly treated.

摘要

我们报告了一例以多发性肌炎典型症状为先兆的男性Churg-Strauss综合征(CSS)患者。在大剂量皮质类固醇治疗(1.5毫克/千克/天)期间,他出现了严重的多发性单神经炎,对免疫球蛋白和甲氨蝶呤治疗反应不佳。6个月后,他出现了右侧坐骨腘肌和桡神经部分功能缺陷。腓肠神经活检显示神经外膜血管有特征性的坏死性血管炎,伴有粒细胞和嗜酸性粒细胞浸润。在CSS病程中,外周神经系统受累很常见,可导致残疾。因此,必须及时识别并妥善治疗。

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