• 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

Reticulated violaceous patches in a 10-year-old boy.

作者信息

Nguyen Cassidy M, Clarke Emily, Peterson Rosemary, Keeling Brett H, Diaz Lucia Z

机构信息

Division of Dermatology, Department of Internal Medicine, Dell Medical School, University of Texas at Austin, Austin, Texas.

Division of Pediatric Rheumatology, Department of Pediatrics, Dell Medical School, University of Texas at Austin, Austin, Texas.

出版信息

JAAD Case Rep. 2024 Oct 11;62:143-145. doi: 10.1016/j.jdcr.2024.09.020. eCollection 2025 Aug.

DOI:10.1016/j.jdcr.2024.09.020
PMID:40778345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12329500/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e395/12329500/e5d86d23de62/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e395/12329500/8666a88c6033/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e395/12329500/87117c637541/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e395/12329500/e5d86d23de62/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e395/12329500/8666a88c6033/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e395/12329500/87117c637541/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e395/12329500/e5d86d23de62/gr3.jpg

相似文献

1
Reticulated violaceous patches in a 10-year-old boy.一名10岁男孩身上的网状紫罗兰色斑块。
JAAD Case Rep. 2024 Oct 11;62:143-145. doi: 10.1016/j.jdcr.2024.09.020. eCollection 2025 Aug.
2
A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-α.一名 9.5 岁男孩出现反复的神经表现和严重高血压,最初被诊断为结节性多动脉炎,随后被诊断为腺苷脱氨酶 2 型缺乏症(DADA2),对 TNF-α 拮抗剂治疗有反应。
Paediatr Int Child Health. 2020 Feb;40(1):65-68. doi: 10.1080/20469047.2018.1559495. Epub 2019 Jan 15.
3
Adenosine Deaminase 2 Deficiency腺苷脱氨酶2缺乏症
4
Early-onset stroke, polyarteritis nodosa (PAN), and livedo racemosa.早发性中风、结节性多动脉炎(PAN)和网状青斑。
J Am Acad Dermatol. 2016 Aug;75(2):449-53. doi: 10.1016/j.jaad.2016.01.057.
5
Deficiency of ADA2 mimicking autoimmune lymphoproliferative syndrome in the absence of livedo reticularis and vasculitis.ADA2 缺乏症模拟无网状青斑和血管炎的自身免疫性淋巴增生综合征。
Pediatr Blood Cancer. 2018 Apr;65(4). doi: 10.1002/pbc.26912. Epub 2017 Dec 22.
6
Cutaneous vasculitis in autoinflammatory diseases.自身炎症性疾病中的皮肤血管炎。
J Dermatol. 2024 Feb;51(2):150-159. doi: 10.1111/1346-8138.17030. Epub 2023 Nov 13.
7
Systematic review of childhood-onset polyarteritis nodosa and DADA2.儿童发病型结节性多动脉炎与 DADA2 的系统综述
Semin Arthritis Rheum. 2021 Jun;51(3):559-564. doi: 10.1016/j.semarthrit.2021.04.009. Epub 2021 Apr 19.
8
Livedo racemosa, secondary to drug-induced systemic lupus erythematosus.网状青斑,继发于药物性系统性红斑狼疮。
Dermatol Online J. 2010 Nov 15;16(11):24.
9
The spectrum of differential diagnosis in neurological patients with livedo reticularis and livedo racemosa. A literature review.患有网状青斑和匐行性血管瘤的神经科患者的鉴别诊断范围。文献综述。
J Neurol. 2005 Oct;252(10):1155-66. doi: 10.1007/s00415-005-0967-9. Epub 2005 Aug 26.
10
Livedo Racemosa: Clinical, Laboratory, and Histopathological Findings in 33 Patients.网状青斑:33例患者的临床、实验室及组织病理学表现
Int J Low Extrem Wounds. 2021 Mar;20(1):22-28. doi: 10.1177/1534734619896938. Epub 2020 Jan 29.

本文引用的文献

1
Evaluation and Management of Deficiency of Adenosine Deaminase 2: An International Consensus Statement.腺苷脱氨酶 2 缺乏症的评估和管理:国际共识声明。
JAMA Netw Open. 2023 May 1;6(5):e2315894. doi: 10.1001/jamanetworkopen.2023.15894.
2
Systematic review of childhood-onset polyarteritis nodosa and DADA2.儿童发病型结节性多动脉炎与 DADA2 的系统综述
Semin Arthritis Rheum. 2021 Jun;51(3):559-564. doi: 10.1016/j.semarthrit.2021.04.009. Epub 2021 Apr 19.
3
Clinical and pathological dermatological features of deficiency of adenosine deaminase 2: A multicenter, retrospective, observational study.
腺苷脱氨酶2缺乏症的临床和病理皮肤特征:一项多中心、回顾性、观察性研究。
J Am Acad Dermatol. 2020 Dec;83(6):1794-1798. doi: 10.1016/j.jaad.2020.03.110. Epub 2020 Apr 10.