• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

间质性肉芽肿性皮炎和栅栏状中性粒细胞性肉芽肿性皮炎的潜在系统性疾病:系统评价。

Underlying Systemic Diseases in Interstitial Granulomatous Dermatitis and Palisaded Neutrophilic Granulomatous Dermatitis: A Systematic Review.

机构信息

Department of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China,

Department of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Dermatology. 2023;239(2):287-298. doi: 10.1159/000527461. Epub 2022 Dec 7.

DOI:10.1159/000527461
PMID:36476409
Abstract

BACKGROUND

Interstitial granulomatous dermatitis (IGD) and palisaded neutrophilic granulomatous dermatitis (PNGD) are uncommon presentations of reactive granulomatous dermatitis. Histologic lesions characterized by IGD/PNGD patterns have been associated with systemic diseases, causing an unmet need for revealing clinical correlates.

OBJECTIVE

The aim of this study was to unravel the systemic diseases beyond dermatitis of IGD/PNGD.

METHODS

This study analyzed data from case studies, case series, and retrospective cohorts by searching PubMed, Embase, Web of Science, and the Cochrane Library, with no start date or language restrictions on Sep 4, 2021.

RESULTS

One hundred ninety-six publications were included (458 cases in total, 216 with details). Systemic diseases associated with IGD/PNGD were classified into 5 groups. Autoimmune disorders (n = 103, 47.6%) including rheumatoid arthritis (n = 51, 23.6%), systemic lupus erythematosus (n = 20, 9.3%), and others were the most common across all underlying diseases, followed by drug eruption (n = 52, 24.1%) such as tumor necrotic factor inhibitor reaction (n = 18, 8.3%) and malignancies (n = 27, 12.5%) such as hematologic malignancy (n = 20, 9.3%). The rest were infectious diseases (n = 12, 5.6%) and accidental conditions (n = 3, 1.4%).

CONCLUSION

IGD/PNGD might be associated with autoimmune disorders, drug eruption, malignancies, infectious diseases, and accidental conditions. Patients with IGD/PNGD need further follow-up.

摘要

背景

间质性肉芽肿性皮炎(IGD)和栅栏状中性粒细胞肉芽肿性皮炎(PNGD)是反应性肉芽肿性皮炎的罕见表现。具有 IGD/PNGD 模式的组织学病变与系统性疾病相关,因此需要揭示其临床相关性。

目的

本研究旨在阐明 IGD/PNGD 之外的系统性疾病。

方法

本研究通过搜索 PubMed、Embase、Web of Science 和 Cochrane Library,分析了病例研究、病例系列和回顾性队列研究的数据,无起始日期或语言限制,截止日期为 2021 年 9 月 4 日。

结果

共纳入 196 篇文献(共 458 例,其中 216 例有详细资料)。与 IGD/PNGD 相关的系统性疾病分为 5 组。自身免疫性疾病(n = 103,47.6%),包括类风湿关节炎(n = 51,23.6%)、系统性红斑狼疮(n = 20,9.3%)和其他疾病;药物反应(n = 52,24.1%),如肿瘤坏死因子抑制剂反应(n = 18,8.3%)和恶性肿瘤(n = 27,12.5%),如血液系统恶性肿瘤(n = 20,9.3%)。其余为感染性疾病(n = 12,5.6%)和意外情况(n = 3,1.4%)。

结论

IGD/PNGD 可能与自身免疫性疾病、药物反应、恶性肿瘤、感染性疾病和意外情况有关。IGD/PNGD 患者需要进一步随访。

相似文献

1
Underlying Systemic Diseases in Interstitial Granulomatous Dermatitis and Palisaded Neutrophilic Granulomatous Dermatitis: A Systematic Review.间质性肉芽肿性皮炎和栅栏状中性粒细胞性肉芽肿性皮炎的潜在系统性疾病:系统评价。
Dermatology. 2023;239(2):287-298. doi: 10.1159/000527461. Epub 2022 Dec 7.
2
Reactive granulomatous dermatitis as a histological pattern including manifestations of interstitial granulomatous dermatitis and palisaded neutrophilic and granulomatous dermatitis: a study of 52 patients.反应性化脓性肉芽肿性皮炎,一种包括间质性化脓性肉芽肿性皮炎、栅栏状中性粒细胞性化脓性肉芽肿性皮炎表现的组织学类型:52 例患者研究。
J Eur Acad Dermatol Venereol. 2021 Apr;35(4):988-994. doi: 10.1111/jdv.17010. Epub 2020 Nov 22.
3
Palisaded Neutrophilic Granulomatous Dermatitis Leading to Diagnosis of Hodgkin Lymphoma: Report of Rare Case and Literature Review of Paraneoplastic Granulomatous Dermatitides.栅栏状中性粒细胞性肉芽肿性皮炎导致霍奇金淋巴瘤的诊断:罕见病例报告及副肿瘤性肉芽肿性皮炎的文献综述
Am J Dermatopathol. 2019 Nov;41(11):835-845. doi: 10.1097/DAD.0000000000001411.
4
Palisaded neutrophilic and granulomatous dermatitis associated with systemic lupus erythematosus: possible involvement of CD163 M2 macrophages in two cases, and a review of published works.与系统性红斑狼疮相关的栅栏状中性粒细胞和肉芽肿性皮炎:两例病例中CD163 M2巨噬细胞可能受累,并对已发表文献进行综述
Lupus. 2018 Dec;27(14):2220-2227. doi: 10.1177/0961203318809892. Epub 2018 Oct 30.
5
Interstitial Granulomatous Dermatitis and Palisaded Neutrophilic Granulomatous Dermatitis: Retrospective Clinicopathological Analysis of 16 Cases.间质性肉芽肿性皮炎和栅栏状中性粒细胞肉芽肿性皮炎:16例回顾性临床病理分析
Dermatol Pract Concept. 2023 Jul 1;13(3):e2023129. doi: 10.5826/dpc.1303a129.
6
Palisaded neutrophilic granulomatous dermatitis with leukocytoclastic vasculitis in a patient without any underlying systemic disease detected to date.在一名迄今为止未检测到任何潜在全身性疾病的患者中出现的伴有白细胞破碎性血管炎的栅栏状嗜中性粒细胞肉芽肿性皮炎。
J Cutan Pathol. 2010 Oct;37(10):1092-7. doi: 10.1111/j.1600-0560.2009.01466.x. Epub 2009 Nov 9.
7
Palisaded neutrophilic granulomatous dermatitis in rheumatoid arthritis.类风湿关节炎中的栅栏状中性粒细胞肉芽肿性皮炎
J Am Acad Dermatol. 2002 Aug;47(2):251-7. doi: 10.1067/mjd.2002.124620.
8
Palisading neutrophilic and granulomatous dermatitis as a presentation of Hodgkin lymphoma: A case and review.栅栏状中性粒细胞和肉芽肿性皮炎作为霍奇金淋巴瘤的一种表现:1例病例及文献复习
J Cutan Pathol. 2018 Feb;45(2):167-170. doi: 10.1111/cup.13076. Epub 2017 Dec 11.
9
Palisaded neutrophilic granulomatous dermatitis, interstitial granulomatous dermatitis and IgA vasculitis associated with incomplete Sjögren's syndrome.与不完全性干燥综合征相关的栅栏状中性粒细胞性肉芽肿性皮炎、间质性肉芽肿性皮炎和IgA血管炎。
J Dermatol. 2021 Apr;48(4):556-558. doi: 10.1111/1346-8138.15738. Epub 2021 Jan 6.
10
Palisaded neutrophilic and granulomatous dermatitis associated with ankylosing spondylitis.与强直性脊柱炎相关的栅栏状中性粒细胞和肉芽肿性皮炎。
Am J Dermatopathol. 2013 Dec;35(8):847-50. doi: 10.1097/DAD.0b013e3182964f26.

引用本文的文献

1
Reactive Granulomatous Dermatitis: A Descriptive Study of 10 Patients.反应性肉芽肿性皮肤病:10 例患者的描述性研究。
J Cutan Med Surg. 2024 Jan-Feb;28(1):33-36. doi: 10.1177/12034754231220937. Epub 2024 Jan 16.
2
Extensive reactive cutaneous histiocytic infiltrate resembling non-Langerhans cell histiocytosis as the presenting sign of underlying vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome.广泛的反应性皮肤组织细胞浸润,类似于非朗格汉斯细胞组织细胞增多症,作为潜在的空泡、E1酶、X连锁、自身炎症性、体细胞综合征的首发体征。
JAAD Case Rep. 2023 Nov 21;43:20-23. doi: 10.1016/j.jdcr.2023.11.008. eCollection 2024 Jan.
3
Interstitial Granulomatous Dermatitis as the Initial Manifestation of Granulomatosis with Polyangiitis.
间质性肉芽肿性皮炎作为肉芽肿性多血管炎的初始表现
Cureus. 2023 Jul 22;15(7):e42293. doi: 10.7759/cureus.42293. eCollection 2023 Jul.