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Palisaded Neutrophilic and Granulomatous Dermatitis in a Patient with Granulomatosis with Polyangiitis

机译:多发性肉芽肿性肉芽肿患者的中性粒细胞性嗜中性粒细胞肉芽肿性皮炎

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摘要

Palisaded neutrophilic and granulomatous dermatitis (PNGD) shows various clinical features and is histologically characterized by palisaded granulomas surrounding degenerated collagen. PNGD is known to be associated with a variety of systemic conditions such as rheumatoid arthritis and systemic lupus erythematosus. Furthermore, PNGD has been reported to be associated with antineutrophilic cytoplasmic antibody-associated vasculitis, including granulomatosis with polyangiitis (GPA) and microscopic polyangiitis. Here, we report a case of PNGD associated with GPA, which showed the infiltration of CD163-positive M2 macrophages in the skin lesion with elevated serum level of soluble CD163 (sCD163). The serum sCD163 level was reduced to normal range after systemic steroid therapy. Thus, M2 macrophages may play a role in the pathomechanisms of PNGD associated with GPA.
机译:偶发性嗜中性粒细胞肉芽肿性皮炎(PNGD)具有多种临床特征,其组织学特征是周围变性胶原周围的栅状肉芽肿。已知PNGD与多种系统性疾病有关,例如类风湿性关节炎和系统性红斑狼疮。此外,据报道PNGD与抗中性粒细胞胞浆抗体相关的血管炎有关,包括肉芽肿伴多血管炎(GPA)和显微镜下的多血管炎。在这里,我们报告一例与GPA相关的PNGD,这表明皮肤病变中CD163阳性M2巨噬细胞浸润,血清可溶性CD163(sCD163)水平升高。全身类固醇治疗后,血清sCD163水平降至正常范围。因此,M2巨噬细胞可能在与GPA相关的PNGD的发病机制中起作用。

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