• 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

过敏性紫癜性脑病

Encephalopathy in Henoch-Schönlein Purpura.

作者信息

Shen Huijun, Mao Jianhua, Shu Qiang, Du Lizhong

机构信息

Departments of Nephrology, *Thoracic and Cardiovascular Surgery, and #Neonatology; The Children's Hospital of Zhejiang University School of Medicine, Hangzhou, China. Correspondence to: Dr JH Mao, Department of Nephrology, The Children's Hospital of Zhejiang University School of Medicine, Hangzhou 310006, Zhejiang Province, China.

出版信息

Indian Pediatr. 2017 Aug 15;54(8):675-677. doi: 10.1007/s13312-017-1132-0.

DOI:10.1007/s13312-017-1132-0
PMID:28891482
Abstract

BACKGROUND

Henoch-Schönlein purpura (HSP) is the most common vasculitis in childhood. Severe central nervous system (CNS) involvement is rare in HSP.

CASE CHARACTERISTICS

Three children with features of HSP presented with seizures and CNS dysfunction.

OBSERVATION

All three children had abnormalities on neuroimaging; 2 had complete remission but one was left with severe neurological damage.

MESSAGE

HSP patients may rarely present with CNS involvement with a prolonged course requiring aggressive treatment.

摘要

背景

过敏性紫癜(HSP)是儿童期最常见的血管炎。严重的中枢神经系统(CNS)受累在HSP中较为罕见。

病例特征

三名具有HSP特征的儿童出现癫痫发作和中枢神经系统功能障碍。

观察结果

所有三名儿童神经影像学检查均有异常;2例完全缓解,但1例遗留严重神经损伤。

启示

HSP患者可能很少出现中枢神经系统受累,病程较长,需要积极治疗。

相似文献

1
Encephalopathy in Henoch-Schönlein Purpura.过敏性紫癜性脑病
Indian Pediatr. 2017 Aug 15;54(8):675-677. doi: 10.1007/s13312-017-1132-0.
2
Neurologic manifestations of Henoch-Schönlein purpura.过敏性紫癜的神经系统表现。
Handb Clin Neurol. 2014;120:1101-11. doi: 10.1016/B978-0-7020-4087-0.00074-7.
3
Gastrointestinal Henoch-Schönlein purpura successfully treated with Mycophenolate Mofetil: Description of 2 case reports.胃肠道型亨诺克-舒恩莱因紫癜经霉酚酸酯成功治疗:2 例病例报告描述。
Medicine (Baltimore). 2021 Jan 8;100(1):e24093. doi: 10.1097/MD.0000000000024093.
4
Posterior reversible encephalopathy syndrome in a child with Henoch-Schonlein purpura.一名患有过敏性紫癜的儿童的后部可逆性脑病综合征
BMJ Case Rep. 2013 Aug 14;2013:bcr2013008900. doi: 10.1136/bcr-2013-008900.
5
Analysis of children with Henoch-Schonlein purpura secondary to infection.感染相关性过敏性紫癜患儿分析。
Clin Rheumatol. 2022 Mar;41(3):803-810. doi: 10.1007/s10067-021-06007-9. Epub 2022 Jan 7.
6
[Clinical Significance of Serum Midkine in Children with Henoch-Schonlein Purpura].[血清中期因子在过敏性紫癜患儿中的临床意义]
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Feb;25(1):181-185. doi: 10.7534/j.issn.1009-2137.2017.01.032.
7
Henoch-Schönlein Purpura in Children: An Updated Review.儿童过敏性紫癜:最新综述。
Curr Pediatr Rev. 2020;16(4):265-276. doi: 10.2174/1573396316666200508104708.
8
Do practical laboratory indices predict the outcomes of children with Henoch-Schönlein purpura?实用实验室指标能否预测儿童过敏性紫癜的结局?
Postgrad Med. 2019 May;131(4):295-298. doi: 10.1080/00325481.2019.1609814. Epub 2019 Apr 25.
9
Pulmonary hemorrhage, a rare complication in a girl with Henoch-Schönlein purpura.肺出血,是一名患有过敏性紫癜的女孩的罕见并发症。
Arch Argent Pediatr. 2016 Oct 1;114(5):e366-9. doi: 10.5546/aap.2016.eng.e366.
10
Central Nervous System Involvement in Henoch-Schonlein Purpura in Children and Adolescents.儿童和青少年过敏性紫癜的中枢神经系统受累情况
Case Rep Pediatr. 2017;2017:5483543. doi: 10.1155/2017/5483543. Epub 2017 Jan 21.

引用本文的文献

1
Immunoglobulin a vasculitis with central nervous system involvement: analysis of 10 cases.伴有中枢神经系统受累的免疫球蛋白A血管炎:10例分析
Clin Exp Med. 2025 May 9;25(1):145. doi: 10.1007/s10238-025-01679-y.
2
Focal Seizures and Posterior Reversible Encephalopathy Syndrome as Presenting Signs of IgA Vasculitis/Henoch-Schoenlein Purpura-An Educative Case and Systematic Review of the Literature.局灶性癫痫发作和后部可逆性脑病综合征作为IgA血管炎/过敏性紫癜的首发症状——一个具有教育意义的病例及文献系统综述
Front Neurol. 2021 Nov 15;12:759386. doi: 10.3389/fneur.2021.759386. eCollection 2021.