儿童脱髓鞘疾病:从多发性硬化到抗髓鞘少突胶质细胞糖蛋白相关脑脊髓炎的新模式

Q4 Medicine
Neurographics Pub Date : 2020-06-01 DOI:10.3174/ng.1900049
J. Aw-Zoretic, A. Harrell, J. Rubin, S. Palasis
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引用次数: 2

摘要

对儿童脱髓鞘疾病的了解正在取得进展,包括最近发现的抗髓鞘少突胶质细胞糖蛋白(抗mog)脑炎。放射科医生在这些患者的诊断工作中起着关键作用。脱髓鞘疾病很难相互区分,并且可以模拟抗mog脑炎,特别是因为各种疾病可以呈现非特异性放射学脊髓表现和重叠的中枢神经系统特征。有一些关键的影像学特征可以解释这些不同实体的病理生理基础的最新发展。注意相关的临床病史可以提高诊断的准确性。在儿科人群中识别特定脱髓鞘诊断的MR成像预测因子可以对治疗产生广泛的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pediatric Demyelinating Disease: Emerging Patterns from Multiple Sclerosis to Anti-Myelin Oligodendrocyte Glycoprotein‐Associated Encephalomyelitis
Ongoing progress is being made in the understanding of pediatric demyelinating diseases, including the recent discovery of anti-myelin oligodendrocyte glycoprotein (anti-MOG) encephalitis. Radiologists play a key role in the diagnostic work-up of these patients. Demyelinating diseases can be challenging to differentiate from each other and can mimic anti-MOG encephalitis, especially because the various disorders can present with nonspecific radiologic cord findings and overlapping CNS features. There are some key imaging features that can be explained by the more recent development in the pathophysiological basis of these different entities. Attention to pertinent clinical history allows for improved diagnostic accuracy. Identifying MR imaging predictors of a particular demyelinating diagnosis in the pediatric population can have broad implications on treatment.
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来源期刊
Neurographics
Neurographics Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
0.20
自引率
0.00%
发文量
12
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