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迟发性拉斯穆森脑炎的磁共振成像:一项长期随访研究

MRI in Late-Onset Rasmussen Encephalitis: A Long-Term Follow-Up Study.

作者信息

Doniselli Fabio Martino, Deleo Francesco, Criscuolo Stefania, Stabile Andrea, Pastori Chiara, Di Giacomo Roberta, Didato Giuseppe, Chiapparini Luisa, Villani Flavio

机构信息

Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133 Milan, Italy.

Department of Biomedical Sciences for Health, University of Milan, Via Mangiagalli 31, 20122 Milan, Italy.

出版信息

Diagnostics (Basel). 2022 Feb 15;12(2):502. doi: 10.3390/diagnostics12020502.

Abstract

Late-onset Rasmussen encephalitis (LoRE) is a rare unihemispheric progressive inflammatory disorder causing neurological deficits and epilepsy. The long-term radiological evolution has never been fully described. We retrospectively analyzed the MR images of 13 LoRE patients from a total of 136 studies, and searched for focal areas of volume loss or signal intensity abnormality in grey matter or white matter. Each subject had a median of nine MRI studies (IQR 7-13). Frontal and temporal lobes were the most affected regions (13/13 and 8/13, respectively) and showed the greatest worsening over time in terms of atrophic changes (9/13 and 5/8, respectively). A milder cortical atrophy was found in the insular and parietal lobes. The caudate nucleus was affected in seven patients. Hyperintensities of grey matter and white matter on T2-WI and FLAIR images were observed in all patients, and transiently in eight patients. In two cases out of the latter patients, these transient alterations evolved into atrophy of the same region. Disease duration was significantly associated with signal abnormalities in the grey matter at last follow-up. LoRE MRI alterations are milder, and their progression is markedly slower compared to radiological findings described in the childhood form.

摘要

迟发性拉斯穆森脑炎(LoRE)是一种罕见的单侧进行性炎症性疾病,可导致神经功能缺损和癫痫。其长期的影像学演变从未得到充分描述。我们回顾性分析了136项研究中13例LoRE患者的磁共振成像(MR)图像,寻找灰质或白质中体积缩小或信号强度异常的局灶性区域。每位受试者的MRI研究中位数为9次(四分位间距7 - 13)。额叶和颞叶是受影响最严重的区域(分别为13/13和8/13),并且随着时间推移在萎缩性改变方面恶化最为明显(分别为9/13和5/8)。在岛叶和顶叶发现较轻的皮质萎缩。7例患者的尾状核受到影响。所有患者在T2加权成像(T2-WI)和液体衰减反转恢复序列(FLAIR)图像上均观察到灰质和白质高信号,8例患者为短暂性高信号。在后一组患者中的2例,这些短暂性改变演变为同一区域的萎缩。疾病持续时间与末次随访时灰质信号异常显著相关。与儿童型拉斯穆森脑炎所描述的影像学表现相比,LoRE的MRI改变较轻,其进展明显较慢。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e4d/8871246/4e3693781d7f/diagnostics-12-00502-g001.jpg

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