BACKGROUND:Rheumatoid neutrophilic dermatitis (RND) is a recently recognized, rare cutaneous manifestation of rheumatoid arthritis. It occurs in patients with severe rheumatoid arthritis and is typically asymptomatic. Rheumatoid neutrophilic dermatitis was originally described by Ackerman in 1978. Since that time, 8 patients with this disease have been described in the literature.

OBSERVATIONS:We report 2 cases of RND. Findings of skin biopsy specimens from both patients revealed characteristic signs of dermal leukocytosis and leukocytoclasia without vasculitis. The pathogenesis of the neutrophilic infiltrate is unclear. Processes that may play a role in the pathogenesis of RND include immune complex activations, cell adhesion and migration, and cytokine release.

CONCLUSIONS:Rheumatoid neutrophilic dermatitis falls into the spectrum of neutrophilic vascular reactions described by Jorizzo and Daniels. Although early reports suggest that prominent leukocytoclasia is not a feature of RND, our findings confirm the observations of Lowe et al that leukocytoclasia can be seen in RND and may be striking. It is important for dermatologists to be aware of this rare manifestation of rheumatoid arthritis.

译文

背景:类风湿性嗜中性皮炎(RND)是类风湿关节炎的一种近来罕见的皮肤表现。它发生在患有严重类风湿关节炎的患者中,通常无症状。类风湿性嗜中性皮炎最初是由Ackerman在1978年描述的。从那时起,文献中已经描述了8例这种疾病的患者。

观察:我们报告了2例RND。两名患者的皮肤活检标本的发现均显示出皮肤白细胞增多和无血管炎的白细胞增多症的特征性体征。中性粒细胞浸润的发病机理尚不清楚。在RND发病机制中可能起作用的过程包括免疫复合物激活,细胞粘附和迁移以及细胞因子释放。

结论:类风湿性中性皮炎属于中性血管的范畴Jorizzo和Daniels描述的反应。尽管早期的报道表明突出的白细胞增多症不是RND的特征,但我们的发现证实了Lowe等人的观察结果,即白细胞增多症可以在RND中发现并且可能很明显。对于皮肤科医生来说,重要的是要意识到这种类风湿关节炎的罕见表现。

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