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散发型Creutzfeldt-Jakob病1例报告 被引量:1

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摘要 Creutzfeldt-Jakob病(CJD)又称皮质-纹状体-脊髓变性,临床少见,现报道1例如下。1病例男,70岁,因"头痛伴视物模糊1个月余,反应迟钝、记忆力减退半月余"于2015年9月28日入院。患者于2015年8月中旬无明显诱因出现头痛,视物模糊,遂至当地医院按脑梗死治疗,头痛稍有好转后出院。9月10日患者症状加重,视物模糊加重并有复视,后逐渐出现反应迟钝,行走迟缓,记忆力减退。
出处 《临床神经病学杂志》 CAS 北大核心 2016年第5期397-399,共3页 Journal of Clinical Neurology
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参考文献12

  • 1孙光林,许利刚,刘晨,李作汉.Creutzfeldt-Jakob病的临床和影像学特点[J].临床神经病学杂志,2012,25(1):14-16. 被引量:3
  • 2Puoti G, Bizzi A, Forloni G, et al. Sporadic human prion diseases: molecular insights and diagnosis[ J]. Lancet Neurol,2012,11:618. 被引量:1
  • 3Parchi P, Giese A, Capellari S, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analy- sis of 300 subjects[J]. Ann Neurol, 1999, 46: 224. 被引量:1
  • 4张萍,李洁,李莉萍.Creutzfeldt-Jakob病的临床、影像学及电生理特点[J].临床神经病学杂志,2015,28(4):265-268. 被引量:8
  • 5Steinhoff B J, Zcrr I, Glatting M, et al. Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease [ J ]. Ann Neurol,2004,56 : 702. 被引量:1
  • 6Muayqil T, Gronseth G, Camicioli R. Evidence-based guideline : diag- nostic accuracy of CSF 14-3-3 protein in sporadic Creutzfeldt-Jakob disease : report of the guideline development subcommittee of the A- merican academy of neurology [ J ]. Neurology,2012,79 : 1499. 被引量:1
  • 7Hamlin C, Puoti G, Berri S, et al. A comparison oftau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob disease[ J]. Neurology, 2012, 79 : 547. 被引量:1
  • 8Wang LH, Bucelli RC, Patrick E, et al. Role of magnetic reso- nance imaging, cerebrospinal fluid, and electroencephalogram in di- agnosis of sporadic Creutzfeldt-Jakob disease [ J ]. J Neurol, 2013, 260 : 498. 被引量:1
  • 9Forner SA, Takada LT, Bettcher BM, et al. Comparing CSF bio- markers and brain MRI in the diagnosis of sporadic Creutzfeldt-Jakoh disease[J]. Neurol Clin Pract, 2015, 5 : 116. 被引量:1
  • 10Vitali P, Maccagnano E, Caverzasi E, et al. Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid de- mentias[J]. Neurology, 2011,76: 1711. 被引量:1

二级参考文献31

  • 1于雪凡,林世和,孙瑞红,赵珩.脑脊液14-3-3蛋白和神经元特异性烯醇化酶对Creutzfeldt-Jakob病的诊断价值[J].临床神经病学杂志,2008,21(6):401-403. 被引量:1
  • 2Brandel JP, Delasnerie-Lanpretre N, Lap lanche JL, et al. Diagnosis of Creutzfeldt Jakob disease: effect of clinical criteria on inci- dence estimates [ J]. Neurology, 2000, 54 : 1095. 被引量:1
  • 3Kay R, Lau WY, Ng HK,et al. Variant Creutzfeldt-Jakob disease in Hong Kong[ J]. Hong Kong Med J, 2001,7:296. 被引量:1
  • 4Kandiah N, Tan K, Pan AB, et al. Creutzfeldt-Jakob disease: wh- ich diffusion-weighted imaging abnormality is associated with period- ic EEG complexes?[J]. J Neurol,2008 ,255 :1411. 被引量:1
  • 5Castellani RJ, Colucci M, XieZ, et al. Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease [ J ]. Neurology, 2004, 63:436. 被引量:1
  • 6Sanchez-Juan P, Sonchez-Valle R, Green A, et al. Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis [J]. JNeurol, 2007, 254:901. 被引量:1
  • 7Satoh K, Shirabe S, Eguchi K. Clinical typing and diagnosis of sporadic human prion diseases (classic sproadic CJD, MM2-cortical form CJD, MM2-thalamic form CJD) [J]. Nippon Rinsho, 2007, 65 : 1423. 被引量:1
  • 8Shiga Y, Miyazawa K, Sato S, et al. Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob dis- ease[J]. Neurology, 2004, 63 : 443. 被引量:1
  • 9Tschampa H J, Zerr I, Urbach H. Radiological assessment of Creutzfeldt-Jakob disease[J]. Eur Radiol. 2007. 17 : 1200. 被引量:1
  • 10Sarac H, Hajnsek S, Basic S, et al. Magnetic resonance spectrosco- py and measurement of tau epitopes of autopsy proven sporadic Creutzfeldt-Jakob disease in a patient with non-specific initial EEG, MRI and negative 14-3-3 immunoblot [ J]. Coil Antropol, 2008, 23 (Supple) : s199. 被引量:1

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