Literature DB >> 33902901

Diffusion-Weighted Imaging is Key to Diagnosing Specific Diseases.

Aya Midori Tokumaru1, Yuko Saito2, Shigeo Murayma3.   

Abstract

This article reviews diseases for which persistent signal abnormalities on diffusion-weighted imaging are the key to their diagnosis. Specifically, updated knowledge regarding the neuroimaging patterns of the following diseases is summarized: sporadic Creutzfeldt-Jakob disease, neuronal intranuclear inclusion disease, and hereditary diffuse leukoencephalopathy with axonal spheroids-colony-stimulating factor receptors/adult-onset leukoencephalopathy with axonal spheroids and pigmented glia. In addition, their differential diagnoses; clinical manifestations; and pathologic, genetic, and imaging correlates are discussed.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Creutzfeldt-Jakob disease; Diffusion-weighted imaging; Hereditary diffuse; Leukoencephalopathy with spheroids-CSF1R; Neuronal intranuclear inclusion body disease

Year:  2021        PMID: 33902901     DOI: 10.1016/j.mric.2021.02.001

Source DB:  PubMed          Journal:  Magn Reson Imaging Clin N Am        ISSN: 1064-9689            Impact factor:   2.266


  2 in total

1.  Two Novel Intronic Mutations in the CSF1R Gene in Two Families With CSF1R-Microglial Encephalopathy.

Authors:  Jiwei Jiang; Wenyi Li; Xiaohong Wang; Zhongli Du; Jinlong Chen; Yaou Liu; Wei Li; Zhonghua Lu; Yanli Wang; Jun Xu
Journal:  Front Cell Dev Biol       Date:  2022-05-24

Review 2.  Clinical and mechanism advances of neuronal intranuclear inclusion disease.

Authors:  Yueqi Liu; Hao Li; Xuan Liu; Bin Wang; Hao Yang; Bo Wan; Miao Sun; Xingshun Xu
Journal:  Front Aging Neurosci       Date:  2022-09-13       Impact factor: 5.702

  2 in total

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