进行性多灶性白质脑病伴高igm综合征1例6岁男孩。

Han Su Kim, Hyun Woo Cho, Yeon Jun Kim, Soo Jin Jung
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摘要

高免疫球蛋白(Ig) M综合征是一种先天性免疫缺陷疾病,其特征是血清IgM升高,血清IgG、IgA和IgE降低。我们报告一个6岁男孩的病例,他患有高igm综合征,作为一种潜在的疾病,在去医院后,由于左上肢肌肉无力,步态障碍和语言障碍,在脑磁共振成像上显示进行性多灶性脑白质病。住院时给予类固醇和静脉注射免疫球蛋白治疗,病情有所好转,但6个月后入院时病情迅速恶化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Progressive Multifocal Leukoencephalopathy With Hyper-IgM Syndrome in a 6-Year-Old Boy.

Hyper-immunoglobulin (Ig) M syndrome is a congenital immunodeficiency disorder characterized by increased serum IgM with low serum IgG, IgA, and IgE. We report the case of a 6-year-old boy with hyper-IgM syndrome as an underlying disease who showed progressive multifocal leukoencephalopathy findings on brain magnetic resonance imaging after visiting the hospital due to left upper extremity muscle weakness, gait disturbance, and speech impairment. At the time of hospitalization, he was treated with steroids and intravenous immunoglobulin, and his condition improved somewhat, but 6 months later, he visited the hospital with rapid deterioration.

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