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一名青少年肺炎支原体感染后出现肌炎、横贯性脊髓炎和吉兰-巴雷综合征并存的情况。

Coexistence of myositis, transverse myelitis, and Guillain Barré syndrome following Mycoplasma pneumoniae infection in an adolescent.

作者信息

Topcu Yasemin, Bayram Erhan, Karaoglu Pakize, Yis Uluc, Guleryuz Handan, Kurul Semra Hiz

机构信息

Department of Pediatrics, Division of Pediatric Neurology, Dokuz Eylul University Medical Faculty, Izmir, Turkey.

出版信息

J Pediatr Neurosci. 2013 Jan;8(1):59-63. doi: 10.4103/1817-1745.111428.

DOI:10.4103/1817-1745.111428
PMID:23772249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3680901/
Abstract

Guillain-Barré syndrome (GBS) and transverse myelitis may occur coexistently in the pediatric population. This may be explained by a shared epitope between peripheral and central nervous system myelin. Coexistent transverse myelitis, myositis, and acute motor neuropathy in childhood have not been previously described. We describe a 14-year-old female patient with transverse myelitis, myositis, and GBS following Mycoplasma pneumoniae infection. She presented with weakness and walking disability. Weakness progressed to involve all extremities and ultimately, she was unable to stand and sit. Based on the clinical findings, a presumptive diagnosis of myositis was made at an outside institution because of high serum creatine kinase level. The patient was referred to our institution for further investigation. Magnetic resonance imaging of spine revealed enhancing hyperintense lesions in the anterior cervicothoracic spinal cord. The electromyography revealed acute motor polyneuropathy. Serum M. pneumoniae IgM and IgG were positive indicating an acute infection. Repeated M. pneumoniae serology showed a significant increase in Mycoplasma IgG titer. The patient was given intravenous immunoglobulin for 2 days and clarithromycin for 2 weeks. She was able to walk without support after 2 weeks of hospitalization. This paper emphasizes the rarity of concomitant myositis, transverse myelitis, and GBS in children.

摘要

吉兰-巴雷综合征(GBS)和横贯性脊髓炎可能同时出现在儿童群体中。这可能是由外周和中枢神经系统髓鞘之间的共同表位所解释。儿童期同时存在横贯性脊髓炎、肌炎和急性运动神经病此前尚未见报道。我们描述了一名14岁女性患者,在感染肺炎支原体后出现横贯性脊髓炎、肌炎和GBS。她表现为虚弱和行走障碍。虚弱进展至累及所有四肢,最终她无法站立和坐下。基于临床表现,在外院因血清肌酸激酶水平高而初步诊断为肌炎。该患者被转诊至我院作进一步检查。脊柱磁共振成像显示颈胸段脊髓前部有强化的高信号病变。肌电图显示急性运动性多发性神经病。血清肺炎支原体IgM和IgG呈阳性,提示急性感染。重复的肺炎支原体血清学检查显示支原体IgG滴度显著升高。该患者接受了2天的静脉注射免疫球蛋白治疗和2周的克拉霉素治疗。住院2周后她能够独立行走。本文强调了儿童同时出现肌炎、横贯性脊髓炎和GBS的罕见性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37f1/3680901/f847dc32764e/JPN-8-59-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37f1/3680901/f847dc32764e/JPN-8-59-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37f1/3680901/f847dc32764e/JPN-8-59-g001.jpg

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Guillain-Barré and Acute Transverse Myelitis Overlap Syndrome Following Obstetric Surgery.产科手术后吉兰-巴雷综合征与急性横贯性脊髓炎重叠综合征
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A Rare Case of Acute Transverse Myelitis (ATM) and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Overlap.急性横贯性脊髓炎(ATM)与急性运动和感觉轴索性神经病(AMSAN)重叠的罕见病例。
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