[摘要]
Background Creutzfeldt-Jakob disease (CJD), a rare disease, is uncharacterized by computed tomography (CT)and magnetic resonance imaging (MRI). This s
BackgroundCreutzfeldt-Jakobdisease(CJD),araredisease,isuncharacterizedbycomputedtomography(CT)andmagneticresonanceimaging(MRI).Thisstudywasaimedtoevaluatethediffusion-weightedMRI(DWI)manifestationsofCJDandtodiscusstheirdiagnosticvalue.MethodsThefindingsofT1-weightedMRI(T1WI),T2-weightedMRI(T2WI),DWIandpost-contrastMRIin5patients(3patientswithbiopsy-provenCJDand2patientswithclinically-provenCJD)wereretrospectivelyanalyzedinthisstudy.ResultsFouroutofthe5patientshadcerebralatrophyofvariousdegrees.Onepatientshowedsymmetrichighsignalintensityatthebilateralglobuspallidusandtheheadofthecaudatenucleus,withveryhighsignalinthecerebralcortexontheDWI.ThispatientonlyhadsymmetricslightlyhighsignalatthebilateralglobuspallidusandputamenonT2WI.OnepatienthadhighsignalintensityatthebasalgangliaandcerebralcortexonDWI,butabnormalT2signalintensityatthebilateralparaventricularwhitematteronMRI.Twopatientspresentedwithwidelygyri-likehighsignalintensityatthecortexonDWI,butroutineMRIshowedbilateralparaventricularlongT2signalintensityin1patientandnoabnormalfindingsinanother.NoabnormalitieswereshownbybothroutineMRIandDWIinthelastpatient.ConclusionsDWIismoresensitivethanitsconventionalcounterpartinthedepictionofCJD.DWIismoresensitivetodetectcorticalabnormalsignalintensityinCJDnotdetectedbyT2WI.