A Rare Case of Anti-Ma2 Antibody-Mediated Autoimmune Encephalomyelitis in Childhood

Q4 Medicine
Han-Sol Kim, M. Yum, Min‐Jee Kim, T. Ko
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引用次数: 0

Abstract

A 9-year-old boy with no relevant previous medical history was admitted to our clinic following 9 days of persistent fever and headache, followed by generalized motor weakness and an altered state of mentality. The patient was initially evalu-ated by a primary care physician and treated with antibiotics, although no improvement was observed. On his first visit to our hospital, he displayed a confused mental state, signs of meninge-al irritation, and decreased motor power (grades I–II) in all extremities on neurologic examinations. Laboratory tests, including thyroid func-tion tests, level of immunoglobulin, and comple-ments, were unremarkable. Brain and spine magnetic resonance imaging (MRI) showed T2 flu-id-attenuated inversion recovery (FLAIR) high signal changes in the basal ganglia, thalami, cor-pus callosum, brainstem, cerebellum, and entire spinal cord with leptomeningeal enhancement (Fig. 1A).
儿童罕见的抗M2抗体介导的自身免疫性脑脊髓炎病例
一名既往无相关病史的9岁男孩因持续发热和头痛9天,随后出现全身性运动无力和精神状态改变而入院。患者最初由初级保健医生评估并使用抗生素治疗,但未观察到任何改善。在他第一次来我们医院时,他表现出精神错乱,脑膜刺激的迹象,神经学检查显示四肢运动能力下降(I-II级)。实验室检查,包括甲状腺功能检查,免疫球蛋白水平和补体,没有显著差异。脑和脊柱磁共振成像(MRI)显示基底节区、丘脑、胼胝体、脑干、小脑和整个脊髓的T2流体衰减反转恢复(FLAIR)高信号改变,并伴有轻脑膜增强(图1A)。
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来源期刊
Annals of Child Neurology
Annals of Child Neurology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.50
自引率
0.00%
发文量
35
审稿时长
8 weeks
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