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一名儿童单纯疱疹病毒1型脑炎痊愈后出现惊吓性癫痫发作和弥漫性白质脑病

Startle Seizures and Diffuse Leukoencephalopathy After Resolution of Herpes Simplex Virus 1 Encephalitis in a Child.

作者信息

Ng Andy Cheuk-Him, Kassiri Janani, Goez Helly R, Morneau-Jacob Francois, Mailo Janette

机构信息

University of Alberta, Edmonton, Canada.

出版信息

Child Neurol Open. 2022 Mar 24;9:2329048X221083761. doi: 10.1177/2329048X221083761. eCollection 2022 Jan-Dec.

Abstract

We describe a unique clinical presentation of a child after the acute phase of herpes simplex virus 1 (HSV1) encephalitis. A 17-month-old boy first presented with HSV1 encephalitis and was promptly treated with antiviral medication. Seven months later, he was re-admitted for startle seizures. Magnetic Resonance Imaging of the brain showed diffuse confluent leukoencephalopathy. This constellation of symptoms has not been previously reported in HSV1 encephalitis. In conclusion, we showed that brain injury due to HSV1 encephalitis can be associated with the development of startle seizures and diffuse white matter injury in the post-acute phase.

摘要

我们描述了一名儿童在单纯疱疹病毒1型(HSV1)脑炎急性期后的独特临床表现。一名17个月大的男孩最初表现为HSV1脑炎,并立即接受了抗病毒药物治疗。七个月后,他因惊吓性癫痫再次入院。脑部磁共振成像显示弥漫性融合性白质脑病。这种症状组合此前在HSV1脑炎中尚未有过报道。总之,我们表明HSV1脑炎所致的脑损伤可能与急性期后惊吓性癫痫的发生及弥漫性白质损伤有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03ea/8961350/01451694f7ba/10.1177_2329048X221083761-fig1.jpg

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