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非典型拉斯穆森脑炎

Atypical Rasmussen's Encephalitis.

作者信息

Alfonso Maria A, Piñeros-Fernández Martha C, Jaimes Luisa F, Ramos Nicolas I

机构信息

Pediatrics, Los Cobos Medical Center, Bogotá, COL.

Pediatric Neurology, Los Cobos Medical Center, Bogotá, COL.

出版信息

Cureus. 2023 Oct 7;15(10):e46647. doi: 10.7759/cureus.46647. eCollection 2023 Oct.

DOI:10.7759/cureus.46647
PMID:37808599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10560088/
Abstract

A three-year-old female patient was admitted to our institution due to subacute fever, intermittent vomiting, persistent bilateral mydriasis after cycloplegia, right central facial palsy, and mild right hemiparesis with hyperreflexia. Brain MRI shows encephalitis in frontal, parietal, insular, and left putamen course and loss of cortical volume and white matter of the entire left hemisphere which are features described in Rasmussen's encephalitis (RE). Therapy with intravenous methylprednisolone bolus was initiated, with adequate clinical response. We consider in this case the diagnosis of atypical RE by imaging criteria in the subacute stage. There are few reports of atypical RE without epilepsy or continuous partial epilepsy. Our purpose is to present a case of a patient with RE images without epilepsy seizures and review the diagnostic and therapeutic approach of RE.

摘要

一名三岁女性患者因亚急性发热、间歇性呕吐、睫状肌麻痹后持续性双侧瞳孔散大、右侧中枢性面瘫以及伴有反射亢进的轻度右侧偏瘫入住我院。脑部磁共振成像显示额叶、顶叶、岛叶及左侧壳核部位存在脑炎,且整个左半球皮质体积和白质减少,这些都是拉斯穆森脑炎(RE)所描述的特征。开始采用静脉注射甲泼尼龙冲击治疗,临床反应良好。我们根据亚急性期的影像学标准考虑该病例为非典型RE。关于无癫痫或持续性部分性癫痫的非典型RE报道较少。我们的目的是呈现一例无癫痫发作的RE影像患者病例,并回顾RE的诊断和治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/36571aab0608/cureus-0015-00000046647-i11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/6d964950e8b7/cureus-0015-00000046647-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/8cd82404858a/cureus-0015-00000046647-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/8004bb383cdb/cureus-0015-00000046647-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/ed910d2910bf/cureus-0015-00000046647-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/c816bbd6cc70/cureus-0015-00000046647-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/fc1196489eba/cureus-0015-00000046647-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/1bdac1157e72/cureus-0015-00000046647-i07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/52c45720011c/cureus-0015-00000046647-i08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/38aed2119c46/cureus-0015-00000046647-i09.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/9b00431fb0ee/cureus-0015-00000046647-i10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/36571aab0608/cureus-0015-00000046647-i11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/6d964950e8b7/cureus-0015-00000046647-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/8cd82404858a/cureus-0015-00000046647-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/8004bb383cdb/cureus-0015-00000046647-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/ed910d2910bf/cureus-0015-00000046647-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/c816bbd6cc70/cureus-0015-00000046647-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/fc1196489eba/cureus-0015-00000046647-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/1bdac1157e72/cureus-0015-00000046647-i07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/52c45720011c/cureus-0015-00000046647-i08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/38aed2119c46/cureus-0015-00000046647-i09.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/9b00431fb0ee/cureus-0015-00000046647-i10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f18b/10560088/36571aab0608/cureus-0015-00000046647-i11.jpg

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本文引用的文献

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A Special Case of Relapsing-Remitting Bilateral Encephalitis: Without Epilepsy, but Responding to Rituximab and with a Brain Biopsy Coinciding with Rasmussen Encephalitis.复发性双侧脑炎的一个特殊病例:无癫痫发作,但对利妥昔单抗有反应且脑活检结果与拉斯穆森脑炎相符
Brain Sci. 2022 Dec 22;13(1):17. doi: 10.3390/brainsci13010017.
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Seizure Outcomes and Reoperation in Surgical Rasmussen Encephalitis Patients.手术性拉森姆脑炎患者的癫痫发作结局和再次手术。
Neurosurgery. 2022 Jul 1;91(1):93-102. doi: 10.1227/neu.0000000000001958. Epub 2022 May 13.
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Rituximab in Rasmussen's encephalitis: A single center experience and review of the literature.
利妥昔单抗治疗拉斯穆森脑炎:单中心经验及文献综述
Epilepsy Behav Rep. 2022 Apr 9;19:100540. doi: 10.1016/j.ebr.2022.100540. eCollection 2022.
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Rasmussen encephalitis: Predisposing factors and their potential role in unilaterality.拉斯穆森脑炎:诱发因素及其在单侧性中的潜在作用。
Epilepsia. 2022 Jan;63(1):108-119. doi: 10.1111/epi.17131. Epub 2021 Nov 24.
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Atypical Presentation of Cerebral Palsy and Seizures: A Case Report on Rasmussen's Encephalitis in an Adolescent.脑瘫与癫痫的非典型表现:一名青少年患拉斯穆森脑炎的病例报告
Cureus. 2021 Mar 4;13(3):e13705. doi: 10.7759/cureus.13705.
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Seizure. 2020 Oct;81:76-83. doi: 10.1016/j.seizure.2020.07.023. Epub 2020 Jul 25.
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