髓鞘少突胶质细胞糖蛋白相关疾病(MOGAD)的高热:一个诊断挑战。

Chadi Azar, Grace Akiki, Sara F Haddad, Anthony Kerbage, Fady Haddad, Gabrielle Macaron
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引用次数: 0

摘要

髓鞘少突胶质细胞糖蛋白(MOG)-IgG相关疾病(MOGAD)的表型谱在过去几年中有所扩大,非典型表型越来越被认识到。发热性脑膜脑炎很少被报道为MOGAD的一个特征,这是一个诊断挑战。我们报告一例24岁女性高热,脑膜脑脊髓炎,持续阳性MOG-IgG,广泛的感染性检查为阴性,并对大剂量静脉注射甲基强的松龙有反应。MOGAD的完整临床谱尚未完全阐明。在表现为发热性脑膜脑炎的患者中,应考虑进行MOG-IgG检测,特别是在感染性检查为阴性的情况下。
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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High fever in myelin oligodendrocyte glycoprotein-associated disorder (MOGAD): A diagnostic challenge.

The phenotypic spectrum of myelin oligodendrocyte glycoprotein (MOG)-IgG associated disorders (MOGAD) has broadened in the past few years, and atypical phenotypes are increasingly recognized. Febrile meningoencephalitis has rarely been reported as a feature of MOGAD and represents a diagnostic challenge. We report the case of 24-year-old women with high-grade fever, meningoencephalomyelitis, and persistently positive MOG-IgG, for whom an extensive infectious work-up was negative and who responded to high-dose intravenous methylprednisolone. The full clinical spectrum of MOGAD is yet to be completely elucidated. In patients presenting with febrile meningoencephalitis, MOG-IgG testing should be considered particularly if infectious work-up is negative.

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CiteScore
4.70
自引率
0.00%
发文量
54
审稿时长
15 weeks
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