Is it Guillain-Barré Syndrome with Extense Leptomenigeal Enhancement?
Teresa Botelho
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引用次数: 0
Abstract
184 Guillain-Barré syndrome (GBS), an acute immune-mediated polyneuropathy characterized by progressive ascending weakness and areflexia,1 occurs in both adult and pediatric populations, but is uncommon in children less than two years of age.1 Cerebrospinal fluid with albumincytological dissociation is a typical feature in GBS, and also a root enhancement may be seen on spinal cord images, obtained by magnetic resonance imaging (MRI).2 We report a case of a 5-months-old healthy infant, admitted to the Emergency Department in 2018, with decreased spontaneous movements of lower limbs, particularly in the left one, with less than 24 hours of evolution. Four days before, she had had a fever, associated with cough and rhinorrhea, without any causal agent having been identified (syncytial respiratory virus, influenza and adenovirus were tested), in a previous observation carried out in another hospital. Clinical examination showed a left lower limb paralysis, without pain on mobilization or inflammatory signs, and myotatic hyporeflexia in both lower limbs, being even more marked on the left. Based on the hypothesis of post-infectious radiculitis, a 1.5 Tesla MRI was performed under sedation (using a low dose of intravenous propofol and dexmedetomidine, maintaining spontaneous breathing), which showed diffuse leptomenigeal enhancement involving the entire height of the cord, surpassing the posterior fossa superiorly, until the cauda equina roots, which were thickened and enhancing after gadolinium administration (Figs. 1 and 2). Lumbar Informações/Informations: Imagem em Neurologia, publicado em Sinapse, Volume 22, Número 4, outubrodezembro 2022. Versão eletrónica em www.sinapse.pt; Image in Neurology, published in Sinapse, Volume 22, Number 4, October-December 2022. Electronic version in www.sinapse.pt © Autor (es) (ou seu (s) empregador (es)) e Sinapse 2022. Reutilização permitida de acordo com CC BY-NC. Nenhuma reutilização comercial. © Author(s) (or their employer(s)) and Sinapse 2022. Re-use permitted under CC BYNC. No commercial re-use.
是伴有广泛性脑电图增强的格林-巴勒综合征吗?
184吉兰-巴罗综合征(GBS)是一种急性免疫介导的多神经病变,以进行性上升无力和反射性松弛为特征,在成人和儿童人群中均有发生,但在两岁以下儿童中并不常见伴有白蛋白细胞学分离的脑脊液是GBS的典型特征,并且在磁共振成像(MRI)获得的脊髓图像上也可以看到根增强我们报告了一例5个月大的健康婴儿,于2018年入院急诊科,下肢自发运动减少,特别是左下肢,进化时间不到24小时。4天前,在另一家医院进行的观察中,她曾发烧,伴有咳嗽和鼻漏,但未发现任何病因(对合胞呼吸道病毒、流感和腺病毒进行了检测)。临床检查表现为左下肢麻痹,无活动疼痛及炎症征象,双下肢肌强直性反射减退,左侧更为明显。基于感染后神经根炎的假设,在镇静状态下(使用低剂量的静脉异丙酚和右美托咪定,维持自主呼吸)进行1.5特斯拉MRI,显示弥漫性轻脑神经增强,包括脊髓的整个高度,超过后窝,直到马尾神经根,在钆给药后增厚和增强(图1和2)。腰椎Informações/信息:Imagem Neurologia, publicado em Sinapse,第22卷,Número 4, outtubrodezembro 2022。vers o eletrónica em www.sinapse.pt;《神经病学中的影像》,发表于《Sinapse》杂志,第22卷第4期,2022年10 - 12月。电子版本www.sinapse.pt©Autor (es) (ou seu (s) empreador (es)) e Sinapse 2022。reuseza o permitida de acordo com CC BY-NC。nenhuman reutilization。©作者(或其雇主)和Sinapse 2022。在CC BYNC下允许重复使用。禁止商业再利用。
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