首页> 外文期刊>Medicine. >Neutrophilic Dermatoses in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A French Multicenter Study of 17 Cases and Literature Review
【24h】

Neutrophilic Dermatoses in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A French Multicenter Study of 17 Cases and Literature Review

机译:抗中性粒细胞胞浆抗体相关性血管炎中的中性粒细胞皮炎:法国多中心研究17例和文献综述。

获取原文
获取外文期刊封面目录资料

摘要

A few reports suggest combination of ANCA-associated vasculitis (AAV) and neutrophilic dermatoses (ND). We aimed to describe the main characteristics of patients presenting with both AAV and ND in a French cohort and through a systematic literature review, and to discuss the possible common pathogenic process involved. We conducted a retrospective study of patients with both conditions. Patients were selected via the French Internal Medicine Society (SNFMI) and the French Vasculitis Study Group (FVSG). A literature review focusing on a combination of both conditions, concentrated only on publications with well-established diagnoses and individual detailed data. Seventeen patients diagnosed with AAV and ND were identified in this cohort. Twelve patients had granulomatosis with polyangiitis (GPA), 4 had microscopic polyangiitis (MPA) and one had eosinophilic GPA (EGPA). Eight patients, all with GPA, displayed pyoderma gangrenosum (PG). Sweet's syndrome was observed in 6 patients (4 with MPA, one with GPA and one with EGPA) and erythema elevatum diutinum in the other three (2 with GPA and 1 with MPA). The literature review identified 33 additional patients with both conditions, including 26 with GPA. Altogether, of the 50 patients (17 from our study and 33 from the literature review), 33 (66%) patients presented with PG associated with GPA in 29 cases (89%). Corticosteroids were the first-line treatment in conjunction with an immunosuppressive agent in most cases. Outcomes were good and a total of 15 patients experienced a relapse. Patients who relapsed were more likely to have ear, nose and throat manifestation than patients who did not [12/15 (80%) relapsing patients vs. 15/35 (43%) non-relapsing patients; p?=?0.03)]. In our stud, the most frequent association concerned GPA and PG. ND should be considered and specifically researched within the spectrum of cutaneous manifestations observed in AAV.
机译:一些报告建议将ANCA相关血管炎(AAV)和中性粒细胞性皮肤病(ND)合并使用。我们旨在通过系统的文献综述来描述法国队列中同时患有AAV和ND的患者的主要特征,并讨论其中可能涉及的常见致病过程。我们对两种情况的患者进行了回顾性研究。通过法国内部医学学会(SNFMI)和法国血管炎研究组(FVSG)选择患者。文献综述着重于两种情况的结合,仅集中于具有明确诊断和个别详细数据的出版物。在该队列中鉴定出十七名诊断为AAV和ND的患者。 12例肉芽肿伴多血管炎(GPA),4例患有显微镜性多血管炎(MPA),一名嗜酸性GPA(EGPA)。八名均患有GPA的患者表现出坏疽性脓皮病(PG)。在6例患者中观察到了Sweet's综合征(4例为MPA,1例为GPA,1例为EGPA),另外3例(2例为GPA,1例为MPA)出现了高等红斑。文献综述确定了33例同时患有两种疾病的患者,其中26例患有GPA。在50例患者中(本研究17例,文献综述33例),有33例(66%)PG与GPA相关的患者29例(89%)。在大多数情况下,皮质类固醇是与免疫抑制剂联用的一线治疗。结果良好,共有15例患者复发。复发患者比没有复发患者[12/15(80%)复发患者和15/35(43%)非复发患者更有可能出现耳鼻喉疾病。 p≥0.03)]。在我们的研究中,最常见的关联涉及GPA和PG。在AAV中观察到的皮肤表现范围内应考虑并特别研究ND。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号