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首页> 外文期刊>European journal of dermatology: EJD >Palisaded neutrophilic and granulomatous dermatitis in a rheumatoid arthritis patient after treatment with adalimumab
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Palisaded neutrophilic and granulomatous dermatitis in a rheumatoid arthritis patient after treatment with adalimumab

机译:阿达木单抗治疗后的类风湿关节炎患者的中性粒细胞性和肉芽肿性皮炎

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摘要

Palisaded neutrophilic and granulomatous dermatitis (PNGD) is a rare disease occurring in patients with autoimmune diseases [1]. The clinical features are characterised by symmetrically distributed, skin coloured to erythematous, macropapular lesions with a smooth, ulcerated surface, mainly located on the extremities [1]. Histopathologically, PNGD is characterised by the presence of leukocyto-clastic vasculitis (LV), with dense neutrophilic infiltrates and degenerated collagen bundles in the early stage and palisaded granulomas with dermal fibrosis and scant neutrophilic debris in the late stage [1]. Here, we present a rheumatoid arthritis (RA) patient who developed PNGD, possibly induced by adalimumab.
机译:阵发性中性粒细胞肉芽肿性皮炎(PNGD)是一种自身免疫性疾病患者中罕见的疾病[1]。临床特征是皮肤呈对称分布,皮肤呈红斑状,大丘疹性病变,表面光滑,溃疡表面,主要位于四肢[1]。从组织病理学的角度来看,PNGD的特征是白细胞碎裂性血管炎(LV)的存在,早期有致密的中性粒细胞浸润和胶原束变性,晚期是具有皮肤纤维化和中性粒细胞碎片少的乳头状肉芽肿[1]。在这里,我们介绍了可能由阿达木单抗诱发的发展为PNGD的类风湿关节炎(RA)患者。

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