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Palisaded neutrophilic and granulomatous dermatitis associated with the initiation of etanercept in rheumatoid arthritis: a case report

机译:类风湿关节炎中与依那西普起始相关的阵发性嗜中性粒细胞肉芽肿性皮炎:病例报告

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Palisaded neutrophilic and granulomatous dermatitis (PNGD) is an unusual entity with variable clinical manifestations and histopathological features. It is associated with a variety of immune-mediated systemic diseases, most commonly in rheumatoid arthritis. We report a 42-year-old female with a long-standing history of rheumatoid arthritis, presenting with multiple pruritic erythematous papules and nodules on the lower legs 1 month after beginning treatment with etanercept. Microscopic examination of a fully developed lesion showed a diffuse dense interstitial lymphohistiocytic infiltrate interspersed with palisaded granulomas consisting of epithelioid histiocytes and multinucleated giant cells surrounding central zones of degenerated collagen, neutrophils and leukocytoclastic debris. A diagnosis of PNGD was made on the basis of typical histopathologic features. Withdrawal of etanercept led to gradual resolution of the skin lesions, with no new skin lesions appearing afterwards. Although the correlation between the use of tumor necrosis factor-α (TNF-α) antagonists and the development of PNGD remains controversial and warrants further investigation, PNGD should be considered in the differential diagnosis of skin eruptions within a setting of anti-TNF-α therapy.
机译:偶发性嗜中性粒细胞肉芽肿性皮炎(PNGD)是一种异常实体,具有不同的临床表现和组织病理学特征。它与多种免疫介导的全身性疾病相关,最常见于类风湿关节炎。我们报告了一位42岁的女性,患有类风湿关节炎历史悠久,在开始使用依那西普治疗1个月后,小腿上出现多处瘙痒性红斑丘疹和小结节。显微镜下观察到完全发展的病灶,弥漫性弥漫性间质性淋巴组织细胞浸润,散布有栅状肉芽肿,肉瘤由上皮样组织细胞和变性胶原,嗜中性粒细胞和白细胞碎屑中心区域周围的多核巨细胞组成。根据典型的组织病理学特征诊断为PNGD。依那西普的撤出导致皮肤病变的逐渐解决,此后没有新的皮肤病变出现。尽管使用肿瘤坏死因子-α(TNF-α)拮抗剂与PNGD的发展之间的相关性仍存在争议,并有待进一步研究,但在一定的抗TNF-α条件下,PNGD在皮肤萌发的鉴别诊断中应予以考虑。治疗。

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