阿尔及利亚的ANCA血管炎

Madridge Journal of Immunology Pub Date : 2019-02-07 DOI:10.18689/MJIM-1000117

S. Gadiri, H. Meriche, A. Alliouch-Kerboua, A. Atik

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引用次数: 0

摘要

结果:患者平均年龄51岁，诊断为:GPA 14例，显微镜下多血管炎(MPA) 21例，EGPA 04例，GPA与MPA重叠征象53例。临床表现以肾脏疾病为主，其次为肺部疾病和风湿病征象。一些患者有心脏受累。p-ANCA 71例(77.2%)，其中抗mpo特异性43例(46.7%)，c-ANCA 21例(22.8%)，其中抗pr3特异性9例(98%)，无2种特异性40例(43.4%)。

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ANCA Vasculitis in Algeria

Results: The mean age of patients was 51 years, the diagnosis was: 14 cases of GPA, 21 cases of microscopic polyangiitis (MPA), 04 cases of EGPA, 53 subjects had signs of overlap between the GPA and MPA. The clinical picture was dominated by renal disease followed by lung disease and rheumatologic signs. Some patients had cardiac involvement. 71 patients had p-ANCA (77, 2%), of which 43 was anti-MPO specificity (46.7%), 21 patients had c-ANCA (22.8%), including 9 with a specific anti-PR3 (98%), 40 patients showed no 2 searched specificities (43.4%).

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Madridge Journal of Immunology

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