• 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

尼泊尔报告的一例罕见克雅氏病病例。

A rare case of Creutzfeldt-Jakob disease reported from Nepal.

作者信息

Neupane Durga, Gupta Prashant Kumar, Subedi Sushil Sharma, Gupta Dilip, Chhetri Sunit

机构信息

B. P. Koirala Institute of Health Sciences Dharan Nepal.

Department of Radiology National Academy of Medical Sciences Bir Hospital Kathmandu Nepal.

出版信息

Clin Case Rep. 2021 Sep 13;9(9):e04804. doi: 10.1002/ccr3.4804. eCollection 2021 Sep.

DOI:10.1002/ccr3.4804
PMID:34532050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8436889/
Abstract

Creutzfeldt-Jakob disease, though rare, should be considered in the clinical picture of rapidly progressive dementia and absence of verbal response as evident in our case despite the absence of typical radiological picture.

摘要

克雅氏病虽然罕见，但在快速进展性痴呆且无言语反应的临床症状中应予以考虑，就像我们这个病例一样，尽管没有典型的影像学表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a24/8436889/112bed050a9d/CCR3-9-e04804-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a24/8436889/6cd1de4eafad/CCR3-9-e04804-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a24/8436889/112bed050a9d/CCR3-9-e04804-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a24/8436889/6cd1de4eafad/CCR3-9-e04804-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a24/8436889/112bed050a9d/CCR3-9-e04804-g002.jpg

相似文献

1
A rare case of Creutzfeldt-Jakob disease reported from Nepal.尼泊尔报告的一例罕见克雅氏病病例。
Clin Case Rep. 2021 Sep 13;9(9):e04804. doi: 10.1002/ccr3.4804. eCollection 2021 Sep.
2
Young-onset sporadic Creutzfeldt-Jakob disease with atypical phenotypic features: a case report.具有非典型表型特征的青年型散发性克雅氏病：一例报告
J Med Case Rep. 2019 May 29;13(1):163. doi: 10.1186/s13256-019-2089-5.
3
Creutzfeldt-Jakob disease: a case report and differential diagnoses.克雅氏病：一例病例报告及鉴别诊断
Hawaii J Med Public Health. 2013 Apr;72(4):136-9.
4
Symptomatic aggravation after corticosteroid pulse therapy in definite sporadic Creutzfeldt-Jakob disease with the feature of Hashimoto's encephalopathy.具有桥本脑病特征的明确散发性克雅氏病患者在接受糖皮质激素冲击治疗后症状加重。
BMC Neurol. 2014 Sep 8;14:179. doi: 10.1186/s12883-014-0179-y.
5
Slow to Respond: A Rapidly Progressive Case of Sporadic Creutzfeldt-Jakob Disease.反应迟缓：一例散发性克雅氏病快速进展病例
Cureus. 2024 Feb 1;16(2):e53381. doi: 10.7759/cureus.53381. eCollection 2024 Feb.
6
Clinical features and diagnosis of the MM2 cortical subtype of sporadic Creutzfeldt-Jakob disease.散发性克雅氏病MM2皮质亚型的临床特征与诊断
Arch Neurol. 2006 Jun;63(6):876-80. doi: 10.1001/archneur.63.6.876.
7
Sporadic Creutzfeldt-Jakob disease in Northern Tasmania.塔斯马尼亚岛北部的散发性克雅氏病
J R Coll Physicians Edinb. 2023 Mar;53(1):35-39. doi: 10.1177/14782715221150580. Epub 2023 Jan 20.
8
Applicability of long-term electroencephalography in pre-mortem diagnosis of Creutzfeldt-Jakob disease: A case report.长期脑电图在克雅氏病生前诊断中的适用性：一例报告
SAGE Open Med Case Rep. 2017 Dec 11;5:2050313X17744482. doi: 10.1177/2050313X17744482. eCollection 2017.
9
A Study of Clinical Profile, Radiological and Electroencephalographic Characteristics of Sporadic Creutzfeldt-Jakob Disease From a Tertiary Care Hospital.一家三级护理医院的散发性克雅氏病临床特征、放射学及脑电图特征研究
Cureus. 2023 Dec 5;15(12):e50008. doi: 10.7759/cureus.50008. eCollection 2023 Dec.
10
[MRI role in Creutzfeldt-Jakob disease: about a case].
Pan Afr Med J. 2019 Feb 28;32:95. doi: 10.11604/pamj.2019.32.95.17819. eCollection 2019.

本文引用的文献

1
The first reported case of Creutzfeldt-Jakob disease from Nepal.尼泊尔首例克雅氏病报告病例。
Clin Case Rep. 2019 Dec 12;8(1):198-202. doi: 10.1002/ccr3.2609. eCollection 2020 Jan.
2
Differential diagnosis with other rapid progressive dementias in human prion diseases.人类朊病毒病与其他快速进展性痴呆的鉴别诊断。
Handb Clin Neurol. 2018;153:371-397. doi: 10.1016/B978-0-444-63945-5.00020-9.
3
Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international study.
脑脊液实时震颤诱导转化检测是散发性克雅氏病的一种强大且可靠的检测方法：一项国际研究。
Ann Neurol. 2016 Jul;80(1):160-5. doi: 10.1002/ana.24679. Epub 2016 Jun 1.
4
Prion Diseases.朊病毒疾病
Continuum (Minneap Minn). 2015 Dec;21(6 Neuroinfectious Disease):1612-38. doi: 10.1212/CON.0000000000000251.
5
Comparing CSF biomarkers and brain MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease.比较脑脊液生物标志物和脑部磁共振成像在散发性克雅氏病诊断中的作用。
Neurol Clin Pract. 2015 Apr;5(2):116-125. doi: 10.1212/CPJ.0000000000000111.
6
White matter involvement in sporadic Creutzfeldt-Jakob disease.散发性克雅氏病的白质受累。
Brain. 2014 Dec;137(Pt 12):3339-54. doi: 10.1093/brain/awu298. Epub 2014 Nov 2.
7
Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA.人类朊病毒病组织学分型的共识分类可可靠鉴定分子亚型：欧洲和美国监测中心间的评估者间研究。
Acta Neuropathol. 2012 Oct;124(4):517-29. doi: 10.1007/s00401-012-1002-8. Epub 2012 Jun 30.
8
Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias.弥散加权 MRI 高信号模式可区分 CJD 与其他快速痴呆症。
Neurology. 2011 May 17;76(20):1711-9. doi: 10.1212/WNL.0b013e31821a4439. Epub 2011 Apr 6.
9
The evaluation of rapidly progressive dementia.快速进展性痴呆的评估
Neurologist. 2011 Mar;17(2):67-74. doi: 10.1097/NRL.0b013e31820ba5e3.
10
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.散发性 Creutzfeldt-Jakob 病的临床诊断标准更新版。
Brain. 2009 Oct;132(Pt 10):2659-68. doi: 10.1093/brain/awp191. Epub 2009 Sep 22.