• 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

一例罕见的小儿肉芽肿性多血管炎合并脾梗死,表现为炎症性肠病。

An unusual case of pediatric granulomatosis with polyangiitis complicated by splenic infarction presenting as inflammatory bowel disease.

作者信息

Pathania Shivany, Rehman Rahiya, Ward Madeleine, Yalcindag Ali, Ross Albert, Herzlinger Michael, Gorbounova Irina

机构信息

Department of Pediatrics, Division of Pediatric Gastroenterology, Nutrition, and Liver Diseases Hasbro Children's Hospital Providence Rhode Island USA.

Department of Pediatrics, Division of Internal Medicine-Pediatrics Hasbro Children's Hospital Providence Rhode Island USA.

出版信息

JPGN Rep. 2024 Jun 17;5(3):398-401. doi: 10.1002/jpr3.12099. eCollection 2024 Aug.

DOI:10.1002/jpr3.12099
PMID:39149179
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11322005/
Abstract

We describe a case of granulomatosis with polyangiitis (GPA) in a 7-year-old-male who initially presented with symptoms concerning for Inflammatory bowel disease. GPA is a rare, multisystemic necrotizing vasculitis involving small arteries and veins. The clinical presentation can be variable given its multisystemic involvement but more commonly involves the upper and lower airways and kidneys. This case highlights rare gastrointestinal symptoms of GPA, further complicated by an additional unique finding of splenic infarction. We hope to raise awareness for this rare illness to assist in diagnosis and treatment, as timely induction of remission can reduce significant morbidity and mortality in the pediatric population.

摘要

我们描述了一例7岁男性的肉芽肿性多血管炎(GPA)病例,该患者最初表现出疑似炎症性肠病的症状。GPA是一种罕见的多系统坏死性血管炎,累及小动脉和静脉。由于其多系统受累,临床表现可能多种多样,但更常见的是累及上、下呼吸道和肾脏。本病例突出了GPA罕见的胃肠道症状,脾脏梗死这一额外的独特发现使其病情更加复杂。我们希望提高对这种罕见疾病的认识,以协助诊断和治疗,因为及时诱导缓解可降低儿科患者的显著发病率和死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcfe/11322005/2205a9af5045/JPR3-5-398-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcfe/11322005/51b4e3cac38b/JPR3-5-398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcfe/11322005/e3c60d8bac80/JPR3-5-398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcfe/11322005/2205a9af5045/JPR3-5-398-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcfe/11322005/51b4e3cac38b/JPR3-5-398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcfe/11322005/e3c60d8bac80/JPR3-5-398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcfe/11322005/2205a9af5045/JPR3-5-398-g003.jpg

相似文献

1
An unusual case of pediatric granulomatosis with polyangiitis complicated by splenic infarction presenting as inflammatory bowel disease.一例罕见的小儿肉芽肿性多血管炎合并脾梗死,表现为炎症性肠病。
JPGN Rep. 2024 Jun 17;5(3):398-401. doi: 10.1002/jpr3.12099. eCollection 2024 Aug.
2
Coexistence of granulomatosis with polyangiitis (GPA) and Crohn's disease or multiorgan manifestation of the same disease?肉芽肿性多血管炎(GPA)与克罗恩病并存,还是同一疾病的多器官表现?
Reumatologia. 2016;54(2):86-90. doi: 10.5114/reum.2016.60219. Epub 2016 Jun 3.
3
Asymptomatic intracardiac mass in a 14-year-old girl with granulomatosis with polyangiitis: Case report.14 岁女孩患肉芽肿性多血管炎,无症状性心内肿块:病例报告。
Pediatr Rheumatol Online J. 2012 Apr 13;10(1):9. doi: 10.1186/1546-0096-10-9.
4
Crinkle-Cut Coronary Arteries in a Patient With Granulomatosis With Polyangiitis.一名患有肉芽肿性多血管炎患者的卷曲状冠状动脉。
JACC Case Rep. 2024 Sep 4;29(17):102499. doi: 10.1016/j.jaccas.2024.102499.
5
Atypical presentation of granulomatosis with polyangiitis: a case report and review of the literature.肉芽肿性多血管炎的非典型表现:一例病例报告及文献复习
AME Case Rep. 2024 Jul 4;8:82. doi: 10.21037/acr-24-47. eCollection 2024.
6
Granulomatosis With Polyangiitis Complicated by Diffuse Alveolar Hemorrhage, Splenic Infarction and Stroke.肉芽肿性多血管炎合并弥漫性肺泡出血、脾梗死和中风。
Cureus. 2022 Oct 9;14(10):e30102. doi: 10.7759/cureus.30102. eCollection 2022 Oct.
7
Limited granulomatosis with polyangiitis presenting as an isolated lung lesion.局限型肉芽肿伴多血管炎表现为孤立性肺病变。
Indian J Pathol Microbiol. 2020 Oct-Dec;63(4):611-614. doi: 10.4103/IJPM.IJPM_831_19.
8
An Unusual Presentation of Limited Granulomatosis with Polyangiitis Involving Vagina and Urethra.局限型肉芽肿性多血管炎累及阴道和尿道的罕见表现。
Case Rep Rheumatol. 2017;2017:9407675. doi: 10.1155/2017/9407675. Epub 2017 Mar 13.
9
Granulomatosis with polyangiitis presenting as a solitary renal mass: a case report.肉芽肿性多血管炎表现为孤立性肾肿块:一例报告。
BMC Nephrol. 2023 Jul 28;24(1):223. doi: 10.1186/s12882-023-03276-1.
10
A Rare Case of Granulomatosis With Polyangiitis Complicated by Splenic Rupture.1例罕见的肉芽肿性多血管炎合并脾破裂病例
Cureus. 2024 Jan 18;16(1):e52536. doi: 10.7759/cureus.52536. eCollection 2024 Jan.

引用本文的文献

1
Pediatric Granulomatosis With Polyangiitis: A Case Report Compared to a Case Review in the Last 10 Years.儿童肉芽肿性多血管炎:1例报告并与过去10年病例回顾对比
Cureus. 2025 Jan 10;17(1):e77239. doi: 10.7759/cureus.77239. eCollection 2025 Jan.

本文引用的文献

1
Granulomatosis With Polyangiitis Complicated by Diffuse Alveolar Hemorrhage, Splenic Infarction and Stroke.肉芽肿性多血管炎合并弥漫性肺泡出血、脾梗死和中风。
Cureus. 2022 Oct 9;14(10):e30102. doi: 10.7759/cureus.30102. eCollection 2022 Oct.
2
Anti-Proteinase 3 Antibodies as a Biomarker for Ulcerative Colitis and Primary Sclerosing Cholangitis in Children.抗蛋白酶 3 抗体作为儿童溃疡性结肠炎和原发性硬化性胆管炎的生物标志物。
J Pediatr Gastroenterol Nutr. 2022 Apr 1;74(4):463-470. doi: 10.1097/MPG.0000000000003359. Epub 2021 Nov 24.
3
Gastrointestinal symptoms as first remarkable signs of ANCA-associated granulomatosis with polyangiitis: a case report and reviews.
胃肠道症状作为 ANCA 相关性血管炎伴肉芽肿病的首发显著征象:病例报告及文献复习。
BMC Gastroenterol. 2021 Apr 8;21(1):158. doi: 10.1186/s12876-021-01730-8.
4
Splenic infarction is not rare in granulomatosis with polyangiitis.脾梗死在肉芽肿伴多血管炎中并不罕见。
Clin Rheumatol. 2020 Jun;39(6):1929-1934. doi: 10.1007/s10067-020-04993-w. Epub 2020 Feb 27.
5
Primary Vasculitis in Childhood: GPA and MPA in Childhood.儿童原发性血管炎:儿童肉芽肿性多血管炎和显微镜下多血管炎
Front Pediatr. 2018 Aug 16;6:226. doi: 10.3389/fped.2018.00226. eCollection 2018.
6
Clinical course and outcomes of childhood-onset granulomatosis with polyangiitis.儿童期起病的肉芽肿性多血管炎的临床病程及转归
Clin Exp Rheumatol. 2017 Mar-Apr;35 Suppl 103(1):202-208. Epub 2016 Oct 6.
7
Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis).儿童肉芽肿性多血管炎(韦格纳肉芽肿)的临床特征。
Pediatr Rheumatol Online J. 2014 May 26;12:18. doi: 10.1186/1546-0096-12-18. eCollection 2014.
8
Asymptomatic appearance of splenic infarction in Wegener's granulomatosis.韦格纳肉芽肿病中脾脏梗死的无症状表现。
Pol J Radiol. 2011 Apr;76(2):43-5.
9
Crohn's disease with inflammatory splenic granuloma.克罗恩病伴炎性脾肉芽肿
J Clin Pathol. 2006 Aug;59(8):889. doi: 10.1136/jcp.2005.032508.
10
An unusual intestinal presentation of C-ANCA/PR-3 positive vasculitis in a child.一名儿童中C-ANCA/PR-3阳性血管炎的罕见肠道表现。
J Pediatr Gastroenterol Nutr. 2005 Mar;40(3):368-70. doi: 10.1097/01.mpg.0000155368.46841.21.