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隐源性机化性肺炎患者的数字血管炎

Digital vasculitis in patients with cryptogenic fibrosing alveolitis.

作者信息

Hodson M E, Haslam P L, Spiro S G, Turner-Warwick M

出版信息

Br J Dis Chest. 1984 Apr;78(2):140-8.

PMID:6722017
Abstract

Twelve patients are described with features of cryptogenic fibrosing alveolitis (CFA) with associated florid digital vasculitis (DV). Nine patients had features of various 'connective tissue disorders' involving systems other than the lung, but three had no such features. The immunological features of these patients with DV have been compared with a group of 17 patients who had CFA alone ('lone CFA') and in whom the same range of special laboratory tests were being undertaken concurrently. The group with DV had a higher erythrocyte sedimentation rate and a higher serum IgM, but the most interesting immunological distinction was an increased prevalence of antinuclear antibodies with a nucleolar staining pattern. In addition, the group with DV also had a greater prevalence of single stranded DNA antibodies and of smooth muscle autoantibodies. Circulating immune complexes were not detected more frequently in the group with vasculitis. Ten of the 12 patients were initially treated with corticosteroids and neither the vasculitis nor the lungs improved. In eight the incapacitating DV responded to immunosuppressants (four) or penicillamine (four). In three of these eight patients the lungs also improved.

摘要

本文描述了12例隐源性纤维化肺泡炎(CFA)合并明显指端血管炎(DV)的患者。9例患者有累及肺部以外系统的各种“结缔组织病”特征,但3例无此类特征。将这些合并DV的患者的免疫学特征与一组17例单纯CFA患者(“孤立性CFA”)进行了比较,这组患者同时也进行了相同范围的特殊实验室检查。合并DV的患者红细胞沉降率更高,血清IgM更高,但最有趣的免疫学差异是核仁染色型抗核抗体的患病率增加。此外,合并DV的患者单链DNA抗体和平滑肌自身抗体的患病率也更高。血管炎组循环免疫复合物的检测频率并未更高。12例患者中有10例最初接受了皮质类固醇治疗,血管炎和肺部情况均未改善。在这8例患者中,导致失能的DV对免疫抑制剂(4例)或青霉胺(4例)有反应。在这8例患者中的3例,肺部情况也有所改善。

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