• 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

相似文献

1
Hereditary thrombotic thrombocytopenic purpura: a case report.遗传性血栓性血小板减少性紫癜：一例报告
Hematol Transfus Cell Ther. 2022 Apr-Jun;44(2):269-271. doi: 10.1016/j.htct.2020.08.007. Epub 2020 Sep 13.
2
Inherited thrombotic thrombocytopenic purpura mimicking immune thrombocytopenic purpura during pregnancy: a case report.孕期表现为免疫性血小板减少性紫癜的遗传性血栓性血小板减少性紫癜：一例报告
J Med Case Rep. 2018 Jan 22;12(1):15. doi: 10.1186/s13256-017-1545-3.
3
Current management of thrombotic thrombocytopenic purpura.血栓性血小板减少性紫癜的当前管理
Curr Opin Hematol. 2008 Sep;15(5):445-50. doi: 10.1097/MOH.0b013e328309ec62.
4
Thrombotic thrombocytopenic purpura presenting with pathologic fracture: a case report.以病理性骨折为表现的血栓性血小板减少性紫癜：一例报告
Transfus Apher Sci. 2014 Aug;51(1):73-6. doi: 10.1016/j.transci.2014.05.003. Epub 2014 Jul 28.
5
Case Report: Rabies Vaccine-Induced Thrombotic Thrombocytopenic Purpura in a Patient With Systemic Lupus Erythematosus.病例报告：红斑狼疮患者接种狂犬病疫苗后引发血栓性血小板减少性紫癜。
Front Immunol. 2022 Apr 25;13:851316. doi: 10.3389/fimmu.2022.851316. eCollection 2022.
6
Acquired Thrombotic Thrombocytopenic Purpura Without Anti-ADAMTS13 Antibody Caused by Influenza A (H1N1) Virus Successfully Treated by Plasma Exchange: A Case Report.获得性血栓性血小板减少性紫癜无抗 ADAMTS13 抗体由甲型流感病毒 (H1N1) 成功治疗血浆置换：一例报告。
Am J Case Rep. 2021 Aug 2;22:e932251. doi: 10.12659/AJCR.932251.
7
Post-Partum Thrombotic Thrombocytopenic Purpura (TTP) in a Patient with known Idiopathic (Immune) Thrombocytopenic Purpura: a case report and review of the literature.一名已知患有特发性（免疫性）血小板减少性紫癜的患者发生产后血栓性血小板减少性紫癜：病例报告及文献综述
J Med Case Rep. 2018 Jun 1;12(1):147. doi: 10.1186/s13256-018-1692-1.
8
Concurrence of immune thrombocytopenic purpura and thrombotic thrombocytopenic purpura: a case report and review of the literature.免疫性血小板减少性紫癜与血栓性血小板减少性紫癜并存：病例报告及文献复习。
J Med Case Rep. 2023 Feb 8;17(1):38. doi: 10.1186/s13256-023-03762-y.
9
Graves disease-induced thrombotic thrombocytopenic purpura: a case report.格雷夫斯病诱发的血栓性血小板减少性紫癜：一例报告
J Med Case Rep. 2019 Dec 13;13(1):377. doi: 10.1186/s13256-019-2307-1.
10
Coexistence of thrombotic thrombocytopenic purpura and immune thrombocytopenic purpura in an Asian woman: a case report.一名亚洲女性同时患有血栓性血小板减少性紫癜和免疫性血小板减少性紫癜：病例报告
J Int Med Res. 2022 Mar;50(3):3000605221085127. doi: 10.1177/03000605221085127.

引用本文的文献

1
Hereditary thrombotic thrombocytopenic purpura mimicking immune thrombocytopenia was revealed by miscarriage-novel compound heterozygous mutations in hTTP.遗传性血栓性血小板减少性紫癜模拟免疫性血小板减少症，由 hTTP 中的新型复合杂合突变引起的流产所揭示。
BMC Med Genomics. 2024 Nov 29;17(1):281. doi: 10.1186/s12920-024-02051-x.

本文引用的文献

1
Recombinant ADAMTS-13: first-in-human pharmacokinetics and safety in congenital thrombotic thrombocytopenic purpura.重组ADAMTS-13：先天性血栓性血小板减少性紫癜的首次人体药代动力学和安全性研究
Blood. 2017 Nov 9;130(19):2055-2063. doi: 10.1182/blood-2017-06-788026. Epub 2017 Sep 14.
2
Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies.血栓性血小板减少性紫癜及相关血栓性微血管病术语标准化的共识。
J Thromb Haemost. 2017 Feb;15(2):312-322. doi: 10.1111/jth.13571. Epub 2017 Jan 30.
3
High prevalence of hereditary thrombotic thrombocytopenic purpura in central Norway: from clinical observation to evidence.挪威中部遗传性血栓性血小板减少性紫癜的高发率：从临床观察到证据。
J Thromb Haemost. 2016 Jan;14(1):73-82. doi: 10.1111/jth.13186. Epub 2016 Jan 8.
4
Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene.先天性血栓性血小板减少性紫癜由 ADAMTS13 基因的新复合杂合突变引起。
Eur J Haematol. 2014 Feb;92(2):168-71. doi: 10.1111/ejh.12197. Epub 2013 Dec 10.
5
ADAMTS13 content in plasma-derived factor VIII/von Willebrand factor concentrates.血浆源性因子 VIII/von Willebrand 因子浓缩物中的 ADAMTS13 含量。
Am J Hematol. 2013 Oct;88(10):895-8. doi: 10.1002/ajh.23527. Epub 2013 Aug 30.
6
Unexpected frequency of Upshaw-Schulman syndrome in pregnancy-onset thrombotic thrombocytopenic purpura.妊娠相关性血栓性血小板减少性紫癜中 Upshaw-Schulman 综合征的意外高频率。
Blood. 2012 Jun 14;119(24):5888-97. doi: 10.1182/blood-2012-02-408914. Epub 2012 Apr 30.
7
Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura.ADAMTS13 的残余血浆活性与先天性血栓性血小板减少性紫癜的表型严重程度相关。
Blood. 2012 Jul 12;120(2):440-8. doi: 10.1182/blood-2012-01-403113. Epub 2012 Apr 23.
8
Natural history of Upshaw-Schulman syndrome based on ADAMTS13 gene analysis in Japan.基于日本 ADAMTS13 基因分析的 Upshaw-Schulman 综合征自然史。
J Thromb Haemost. 2011 Jul;9 Suppl 1:283-301. doi: 10.1111/j.1538-7836.2011.04341.x.
9
ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura.ADAMTS13 突变和多态性与先天性血栓性血小板减少性紫癜。
Hum Mutat. 2010 Jan;31(1):11-9. doi: 10.1002/humu.21143.
10
Clinical practice. Thrombotic thrombocytopenic purpura.临床实践。血栓性血小板减少性紫癜。
N Engl J Med. 2006 May 4;354(18):1927-35. doi: 10.1056/NEJMcp053024.

Hereditary thrombotic thrombocytopenic purpura: a case report.

作者信息

Borborema Tarcísio S, Diniz Sabrina Stephanie L, Lima Joziele de S, Costa Fernanda F, Murao Mitiko, Campos Marcia K

机构信息

Hospital Infantil João Paulo II, Belo Horizonte, MG, Brazil.

Hospital Infantil João Paulo II, Belo Horizonte, MG, Brazil.

出版信息

Hematol Transfus Cell Ther. 2022 Apr-Jun;44(2):269-271. doi: 10.1016/j.htct.2020.08.007. Epub 2020 Sep 13.

DOI:10.1016/j.htct.2020.08.007
PMID:33028508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9123582/
Abstract
摘要