Grau-Rivera Oriol, Sánchez-Valle Raquel, Bargalló Nuria, Lladó Albert, Gaig Carles, Nos Carlos, Ferrer Isidre, Graus Francesc, Gelpi Ellen
Neurological Tissue Bank of the Biobanc-Hospital Clínic-Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain.
Alzheimer disease and other cognitive disorders Unit, Department of Neurology, Hospital Clínic, IDIBAPS, Barcelona, Spain.
Neuropathology. 2016 Apr;36(2):199-204. doi: 10.1111/neup.12261. Epub 2015 Nov 6.
In sporadic Creutzfeldt-Jakob disease (sCJD), high signal intensity in fluid attenuated inversion recovery (FLAIR) and diffusion-weighted imaging (DWI) sequences in striatum and/or cortical regions of the brain are present in about 83% of cases, reflecting tissue damage, such as spongiform change and abnormal prion protein deposits. Novel diffusion sequences of MRI might improve the detection of CJD characteristic changes in the subset of patients in whom these alterations are absent or less evident. We report a neuropathologically confirmed case of the rare MM2 T + C subtype of sCJD, with mixed clinical and neuropathological features of MM2 thalamic and MM2 cortical subtypes, in whom the use of diffusion tensor imaging helped to identify cortical hyperintensities that could be easily overlooked with conventional DWI.
在散发性克雅氏病(sCJD)中,约83%的病例在脑纹状体和/或皮质区域的液体衰减反转恢复(FLAIR)序列和扩散加权成像(DWI)序列中出现高信号强度,这反映了组织损伤,如海绵状改变和异常朊蛋白沉积。MRI的新型扩散序列可能会提高对这些改变不存在或不太明显的患者亚组中CJD特征性变化的检测。我们报告了一例经神经病理学证实的罕见的sCJD MM2 T + C亚型病例,具有MM2丘脑亚型和MM2皮质亚型的混合临床和神经病理学特征,在该病例中,使用扩散张量成像有助于识别常规DWI容易忽略的皮质高信号。