小儿比克斯塔夫脑炎1例报告。

IF 3.2 Q2 CLINICAL NEUROLOGY
Luca Gregorio Giaccari, Donatella Mastria, Rosella Barbieri, Rossella De Maglio, Francesca Madaro, Gianfranco Paiano, Luciana Mascia, Maria Caterina Pace, Giuseppe Pulito, Pasquale Sansone
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引用次数: 0

摘要

背景:比克斯塔夫脑干脑炎(BBE)是一种罕见的自身免疫性疾病,文献中报道了大约74例,主要发生在儿童。方法:我们按照CARE指南报道本病例。结果:一名13岁女性,有持续发热和幻觉4天的病史。她迅速发展为眼球震颤,伴有视力模糊和步态共济失调。她还出现精神状态改变、上睑下垂、复视和外源性眼动。脑电图显示脑电活动不对称,左脑半球出现缓慢和尖状异常。腰椎穿刺显示轻度淋巴细胞增多,以淋巴细胞为主,蛋白升高,血糖正常。抗gm1和抗gm2抗体阳性。因怀疑BBE,给予静脉注射免疫球蛋白治疗,精神状态迅速改善。结论:BBE是一种排除性诊断,尤其在儿童年龄时应予以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Case of Bickerstaff Encephalitis in Childhood: A Case Report.

Background: Bickerstaff brainstem encephalitis (BBE) is a rare autoimmune disease and approximately 74 cases have been reported in the literature, mostly in childhood. Methods: We reported this case report according to the CARE guidelines. Results: A 13-year-old female presented with a 4-day history of persistent fever and hallucinations. She rapidly developed nystagmus associated with blurred vision with ataxic gait. She also developed altered mental status, blepharoptosis, diplopia and extrinsic ocular motility. An EEG showed asymmetric brain electrical activity with slow and spiky abnormalities in the left cerebral hemisphere. Lumbar puncture showed mild pleocytosis with lymphocytic predominance, elevated protein, with normal glucose. Anti-GM1 and anti-GM2 antibodies were positive. She was administered intravenous immunoglobulin therapy due to a suspicion of BBE, showing rapid improvement in mental status. Conclusions: BBE is a diagnosis of exclusion and should be considered especially in pediatric age.

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来源期刊
Neurology International
Neurology International CLINICAL NEUROLOGY-
CiteScore
3.70
自引率
3.30%
发文量
69
审稿时长
11 weeks
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