髓鞘少突胶质细胞糖蛋白抗体相关疾病表现为复发性急性播散性脑脊髓炎:文献中最年轻的墨西哥患者的病例报告

Q4 Immunology and Microbiology
Christian García-Estrada, Enrique Gómez-Figueroa, Juan Pablo Morelos-Cisneros, Alondra Deras-Martinez
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引用次数: 0

摘要

髓鞘少突胶质细胞糖蛋白抗体相关疾病髓鞘少突胶质细胞糖蛋白抗体相关疾病是一种新兴的脱髓鞘疾病,不同于神经脊髓炎视谱障碍和多发性硬化症,影响儿童和成人,临床表现包括视神经炎、脊髓炎和急性播散性脑脊髓炎。病例报告我们描述了一个2岁的女孩被诊断为髓鞘少突胶质细胞糖蛋白抗体相关疾病,表现为复发性急性播散性脑脊髓炎,她在接受利妥昔单抗治疗后表现出疾病活动的抑制。该病例是迄今为止报道的最年轻的墨西哥髓鞘少突胶质细胞糖蛋白抗体相关疾病患者。结论了解不同人群的临床表现及其演变,有助于更好地了解该疾病的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myelin oligodendrocyte glycoprotein antibody-associated disease presenting as recurrent acute disseminated encephalomyelitis: Case report of the youngest Mexican patient in the literature

Background

Myelin oligodendrocyte glycoprotein antibody-associated disease myelin oligodendrocyte glycoprotein antibody-associated disease is an emerging demyelinating condition distinct from neuromyelitis optica spectrum disorder and multiple sclerosis affecting both children and adults with a spectrum of clinical manifestations ranging from optic neuritis, myelitis and acute disseminated encephalomyelitis.

Case report

We describe the case of a 2 year-old girl diagnosed with myelin oligodendrocyte glycoprotein antibody-associated disease presenting as recurrent acute disseminated encephalomyelitis who showed suppression of disease activity after treatment with rituximab. This case represents the youngest Mexican patient with myelin oligodendrocyte glycoprotein antibody-associated disease reported to date.

Conclusions

Information regarding the clinical presentation and evolution among different population could help to a better understanding of the presentation of this entity.

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来源期刊
Clinical and Experimental Neuroimmunology
Clinical and Experimental Neuroimmunology Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
1.60
自引率
0.00%
发文量
52
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