Autosomaldominantpolycystickidneydisease常染色体显性遗传多囊肾
来源:双语学影像;病例选自《MayoClinicBodyMRICaseReview》
History47-year-oldwomanwithageneticdisorder
Fig2.1.1CoronalSSFSE
Fig2.1.2axialT1WIFSE
Fig2.1.3Axialfat-saturated2DSSFPimages
ImagingFindingsCoronalSSFSE(Figure2.1.1)andaxialT1-weightedFSE(Figure2.1.2)imagesdemonstrateinnumerablevariable-sizedcyststhroughouttheliverandkidneys.SomecystsshowhighT1-signalintensity.Axialfat-saturated2DSSFPimages(Figure2.1.3)showsimilarfindingsanddemonstratepatencyoftheintrahepaticIVC.
冠状位SSFSE序列和横断位T1WIFSE序列示肝脏及肾脏内布满大量大小不等的囊性病灶,部分囊于T1WI呈高信号。横断位脂肪抑制2DSSFP图像示下腔静脉肝内段通畅。
Diagnosis
Autosomaldominantpolycystickidneydisease
常染色体显性遗传多囊肾
CommentADPKDisarelatively