期刊文献+

扩散加权成像诊断散发性Creutzfeldt-Jakob病价值

Diagnostic value of diffusion-weighted imaging on sporadic Creutzfeldt-Jakob disease
下载PDF
导出
摘要 目的评价扩散加权成像(DWI)对散发性Creutzfeldt-Jakob病的临床诊断价值。方法回顾性分析21例临床诊断为很可能Creutzfeldt-Jakob病患者临床和MRI资料,总结其DWI特征。结果21例散发性Creutzfeldt-Jakob病患者DWI表现为大脑皮质"飘带"样高信号、尾状核和(或)豆状核高信号。异常信号发生部位以大脑皮质合并基底节区最常见(16例,76.19%),单纯皮质受累3例(14.29%)、单纯基底节区受累2例(9.52%);大脑皮质病灶中以额叶受累最常见(15例,78.95%),其次依次为顶叶(13例,68.42%)、颞叶(12例,63.16%)和枕叶(9例,47.37%)。与常规MRI相比,DWI显示病灶更清晰,病灶部位表观扩散系数值下降。21例中5例随访时,DWI高信号强度和范围有所变化,仅1例异常信号范围缩小。结论散发性Creutzfeldt-Jakob病的DWI表现具有一定特异性,推荐作为拟诊散发性Creutzfeldt-Jakob病的检查方法。 Objective To explore the diagnostic value of diffusion-weighted imaging (DWI) on sporadic Creutzfeldt-Jakob disease (sCJD). Methods The MRI findings of 21 patients with clinically proved probable sCJD were analyzed retrospectively and the characteristics were summarized especially in DWI. Results 1) All 21 cases of sCJD were shown abnormal in DWI, which appeared as linear hyperintensity signals in cerebral cortex and patchy hyperintensity in eaudate nucleus and (or) lenticular nucleus. 2) The abnormal signals were most commonly seen in cerebral cortex accompanied with the basal ganglia (16 cases, 76.19%). Besides, there were 3 cases of cortex involvement (14.29%) and 2 cases of basal ganglia involvement (9.52%). Among the lesions in cerebral cortex, the frontal and parietal lobes were affected more commonly (15 cases, 78.95%; 13 cases, 68.42%) than the temporal and occipital lobes (12 cases, 63.16%; 9 cases, 47.37%). 3) DWI was superior to T1WI, T2WI and FLAIR imaging sequences. The abnormal signals in DWI were accompanied by decreased apparent diffusion coefficient (ADC) values. 4) During the follow-up in 5 patients, the range and intensity of high signal changed in DWI, and only one case presented reduced range of abnormal signal. Conclusions sCJD manifests characteristic changes on DWI, which should be suggested as an essential tool for diagnosing sCJD.
出处 《中国现代神经疾病杂志》 CAS 2014年第4期316-321,共6页 Chinese Journal of Contemporary Neurology and Neurosurgery
关键词 克-亚综合征 磁共振成像 Creutzfeld-Jakob syndrome Magnetic resonance imaging
  • 相关文献

参考文献19

  • 1Finkenstaedt M,Szudra A,Zerr I,Poser S,Hise JH,Stoebner JM,Weber T.MR imaging of Creutzfeldt-Jakob disease.Radiology,1996,199:793-798.
  • 2World Health Organization.Manual for surveillance of human transmissible spongiform encephalopathies including variant Creutzfeldt-Jakob disease:World Health Organization communicable disease surveillance and response.Geneva:WHO,2003i 71-72.
  • 3Prusiner SB.Shattuck lecture:neurodegenerative diseases and prions.N Engl J Med,2001,344:1516-1526.
  • 4Zerr I,Kallenberg K,Summers DM,Romero C,Taratuto A,Heinemann U,Breithaupt M,Varges D,Meissner B,Ladogana A,Schuur M,Haik S,Collins SJ,Jansen GH,Stokin GB,Pimentel J,Hewer E,Collie D,Smith P,Roberts H,Brandel JP,van Duijn C,Poeehiari M,Begue C,Cras P,Will RG,Sanchez-Juan P.Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.Brain.2009,132fPt 10-:2659-2668.
  • 5林世和.Creutzfeldt—Jakob病的诊断进展[J].中华神经科杂志,2009,42(5):293-295. 被引量:10
  • 6Josephson SA,Papanastassiou AM,Berger MS,Barbaro NM,McDermott MW,Hilton JF,Miller BL,Geschwind MD.The diagnostic utility of brain biopsy procedures in patients with rapidly deteriorating neurological conditions or dementia.J Neurosurg,2007,106:72-75.
  • 7Mao-Draayer Y,Braff SP,Nagle KJ,Pendlebury W,Penar PL,Shapiro RE.Emerging patterns of diffusion-weighted MR imaging in Creutzfeldt-Jakob disease:case report and review of the literature.AJNR Am J Neuroradiol,2002,23:550-556.
  • 8Young GS,Geschwind MD,Fischbein N J,Martindale JL,Henry RG,Liu S,Lu Y,Wong S,Liu H,Miller BL,Dillon WP.Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease:high sensitivity and specificity for diagnosis.AJNR Am J Neuroradiol,2005,26:1551-1562.
  • 9Shiga Y,Miyazawa K,Sato S,Fukushima R,Shibuya S,Sato Y,Konno H,Doh-ura K,Mugikura S,Tamura H,Higano S,Takahashi S,Itoyama Y.Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease.Neurology,2004,63:443-449.
  • 10Calvar JA,Meli FJ,Romero C,Calcagno ML,Y6nez P,Martinez AR,Lambre H,Taratuto AL,Sevlever G.Characterization of brain tumors by MRS,DWI and Ki-67 labeling index.J Neurooncol,2005,72:273-280.

二级参考文献20

  • 1李硕,赵节绪,林世和,南善姬,江新梅,宋晓南.散发性Creutzfeldt-Jakob病23例临床分析[J].脑与神经疾病杂志,2007,15(1):1-3. 被引量:6
  • 2林世和,于雪凡,孙瑞红,高金立.脑脊液神经蛋白质对临床拟诊Creutzfeldt—Jakob病的早期诊断价值[J].中华神经科杂志,2007,40(4):253-256. 被引量:9
  • 3Hort J, Valis M, Waberzinek G, et al. Proportion oftau protein to phosphorylated tau protein CSF levels in differential diagnosis of dementia. Nervenarzt, 2008, 79: 891-892, 894-896, 898.
  • 4Satoh K, Shirabe S, Tsujino A, et al. Total tan protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt-Jakob disease. Dement Geriatr Cogn Disord, 2007, 24: 207-212.
  • 5Sanchez-Juan P, Sanchez-Valle R, Green A, et al. Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis. J Neurol, 2007, 254: 901-906.
  • 6Castellani RJ, Colueci M, Xie Z, et al. Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease. Neurology, 2004, 63: 436-442.
  • 7Hung CI, Wang PS, Soong BW, et al. Blind source separation of concurrent disease related patterns from EEG in Creutzfeldt-Jakob disease for assisting early diagnosis. Ann Biomed Eng, 2007, 35 : 2168-2179.
  • 8Eggenberger E. Prion disease. Neurol Clin, 2007, 25: 833-842.
  • 9Gertz HJ, Henkes H, Cervos-Navarro J. Creutzfeldt-Jakob disease: correlation of MRI and neuropathologic findings. Neurology, 1988, 38: 1481-1482.
  • 10Kandiah N, Nagaendran K, Tan K, et al. Creutzfeldt-Jakob disease: which diffusion-weighted imaging abnormality is associated with periodic EEG complexes? J Neurol, 2008, 255: 1411-1414.

共引文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部