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抗 GM1 IgM 抗体阳性的轴索型格林-巴利综合征在伴有登革热的儿科患者中。

Anti-GM1 IgM antibody positive axonal variant of Guillain-Barre-syndrome in a pediatric patient with dengue fever.

机构信息

Section of Adult Neurology, Department of Neurosciences, College of Medicine and Philippine General Hospital, University of the Philippines- Manila, Manila, Philippines; Department of Epidemiology and Biostatistics, College of Public Health, University of the Philippines Manila, Manila, Philippines; Division of Neurophysiology, Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.

Department of Pediatrics, Urdaneta District Hospital, Urdaneta City, Pangasinan, Philippines.

出版信息

J Neuroimmunol. 2021 Jun 15;355:577572. doi: 10.1016/j.jneuroim.2021.577572. Epub 2021 Apr 13.

Abstract

INTRODUCTION

While children of all ages may be affected by Guillain-Barre-Syndrome (GBS), there are no reports of Dengue Fever (DF) as the preceding or concurrent infection in this age group. In addition, the presence of anti-GM1 IgM antibody, commonly seen in Multifocal Motor Neuropathy, is rarely encountered in both axonal and demyelinating variants of GBS. Moreover, only few neuromuscular ultrasound findings of the axonal variant in children were reported in the literature.

CASE

Here we present a nine-year-old female who developed the classic signs, symptoms and neurophysiologic findings of axonal type of GBS during DF. She had elevated anti-GM1 IgM antibody atypical of this variant and diffusely enlarged nerves via neuromuscular ultrasound.

CONCLUSION

In a pediatric patient with DF and acute flaccid paralysis, GBS should always be one of the considerations. Although rare, anti-ganglioside GM1 IgM antibody can still be found in axonal variant of GBS.

摘要

简介

虽然所有年龄段的儿童都可能受到格林-巴利综合征(GBS)的影响,但在该年龄组中,没有登革热(DF)作为前驱或并发感染的报告。此外,多灶性运动神经病中常见的抗 GM1 IgM 抗体在 GBS 的轴索性和脱髓鞘性变异体中很少见。此外,文献中仅报道了少数儿童轴索性变异体的神经肌肉超声表现。

病例

在这里,我们介绍了一名 9 岁女性,她在 DF 期间出现了典型的 GBS 轴索性的体征、症状和神经生理学表现。她的抗 GM1 IgM 抗体升高,不典型于这种变异体,神经肌肉超声显示神经弥漫性增大。

结论

在患有 DF 和急性弛缓性瘫痪的儿科患者中,GBS 始终应是其中一种考虑因素。虽然罕见,但抗神经节苷脂 GM1 IgM 抗体仍可在 GBS 的轴索性变异体中发现。

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