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嗜中性荨麻疹性皮肤病和类Sweet嗜中性皮肤病:红斑狼疮中未被充分认识的嗜中性皮肤病

Neutrophilic urticarial dermatosis and Sweet-like neutrophilic dermatosis: under-recognized neutrophilic dermatoses in lupus erythematosus.

作者信息

Lee W J, Kang H J, Shin H J, Won C H, Chang S E, Choi J H, Lee M W

机构信息

423078 Department of Dermatology, Asan Medical Center , University of Ulsan College of Medicine, Seoul, Korea.

出版信息

Lupus. 2018 Apr;27(4):628-636. doi: 10.1177/0961203317736145. Epub 2017 Oct 23.

Abstract

Background/Objectives Neutrophilic dermatoses can be associated with autoimmune connective tissue diseases such as systemic lupus erythematosus (SLE). We analyzed clinical and histological features of neutrophilic urticarial dermatosis (NUD) and Sweet-like neutrophilic dermatosis (SLND)-the most recently delineated entities of the neutrophilic dermatoses. Methods We retrieved database medical records of patients with SLE whose skin biopsy demonstrated a neutrophilic-predominant infiltrate of the skin, and included those whose biopsies revealed findings of SLND or NUD. Results SLND skin lesions lasted longer than those of NUD and were localized to sun-exposed areas. All NUD cases resolved within one week either spontaneously or with treatment such as antihistamines, but SLND skin lesions lasted longer than one week; prednisone was used in four of these five patients. All NUD cases were found in existing SLE patients and were not associated with systemic signs of flare-up of SLE. However, 80% of SLND cases experienced flare-up of SLE; and in 60%, SLND developed concomitantly with SLE as a presenting sign. Conclusion Different clinical courses and relationships with SLE suggest that NUD and SLND have different pathogeneses for neutrophilic inflammatory reactions.

摘要

背景/目的 嗜中性皮病可与自身免疫性结缔组织病相关,如系统性红斑狼疮(SLE)。我们分析了嗜中性荨麻疹性皮病(NUD)和Sweet样嗜中性皮病(SLND)的临床和组织学特征,这是嗜中性皮病中最新界定的类型。方法 我们检索了皮肤活检显示皮肤以嗜中性粒细胞为主浸润的SLE患者的数据库病历,并纳入活检显示SLND或NUD结果的患者。结果 SLND皮肤病变持续时间比NUD长,且局限于暴露于阳光的部位。所有NUD病例在一周内自发缓解或经抗组胺药等治疗后缓解,但SLND皮肤病变持续时间超过一周;这5例患者中有4例使用了泼尼松。所有NUD病例均在现有的SLE患者中发现,且与SLE病情加重的全身症状无关。然而,80%的SLND病例出现SLE病情加重;60%的病例中,SLND与SLE同时出现作为首发症状。结论 不同的临床病程以及与SLE的关系表明,NUD和SLND在嗜中性粒细胞炎症反应方面有不同的发病机制。

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