Recurrent bilateral cortical encephalitis in an adult patient: a case report of delayed diagnosis of myelin oligodendrocyte glycoprotein immunoglobulin G-associated disease
Author:
Funder
Projects in Science and Technique Plans of Xingtai City
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-022-11246-0.pdf
Reference15 articles.
1. Fujimori J, Takai Y, Nakashima I et al (2017) Bilateral frontal cortex encephalitis and paraparesis in a patient with anti-MOG antibodies. J Neurol Neurosurg Psychiatry 88:534–536. https://doi.org/10.1136/jnnp-2016-315094
2. Hamid SHM, Whittam D, Saviour M et al (2018) Seizures and encephalitis in myelin oligodendrocyte glycoprotein IgG disease vs aquaporin 4 IgG disease. JAMA Neurol 75:65–71. https://doi.org/10.1001/jamaneurol.2017.3196
3. Ogawa R, Nakashima I, Takahashi T et al (2017) MOG antibody-positive, benign, unilateral, cerebral cortical encephalitis with epilepsy. Neurol Neuroimmunol Neuroinflammat 4:e322. https://doi.org/10.1212/NXI.0000000000000322
4. Wang L, Zhang B, Zhou L et al (2019) Encephalitis is an important clinical component of myelin oligodendrocyte glycoprotein antibody associated demyelination: a single-center cohort study in Shanghai China. Eur J Neurol 26:168–174. https://doi.org/10.1111/ene.13790
5. Nie HB, Gao HF, Li YQ et al (2021) The clinical features of FLAIR-hyperintense lesions in Anti-MOG antibody associated cerebral cortical encephalitis with seizures: case reports and literature review. Medicine 100:e26087. https://doi.org/10.1097/MD.0000000000026087
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