A burning encephalitis: Fluid-attenuated inversion recovery-hyperintense lesions in Anti-myelin oligodendrocyte glycoprotein-associated encephalitis with seizures in anti-myelin oligodendrocyte glycoprotein-associated encephalitis with seizures-A case report and review of the literature

被引:0
|
作者
El Ouali, Ibtissam [1 ,2 ,4 ]
Naggar, Amine [1 ,2 ]
Berrada, Kenza [1 ,2 ]
Jiddane, Mohamed [1 ,2 ]
Touarsa, Firdaous [1 ,3 ]
机构
[1] Ibn Sina Hosp, Sale, Morocco
[2] Specialty Hosp Rabat, Neuroradiol Dept, Rabat, Morocco
[3] Ibn Sina Hosp, Dept Internal Med, Sale, Morocco
[4] Lalla Asmaa Ave, Sale 11010, Morocco
来源
SAGE OPEN MEDICAL CASE REPORTS | 2024年 / 12卷
关键词
Focal encephalitis; MOGAD; demyelination; ASL hyper-perfusion; MRI FLAIR; differential diagnosis; MOG; ABNORMALITIES; ANTIBODIES; SPECTRUM; FEATURES; DISEASE; ADULTS;
D O I
10.1177/2050313X241261021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
FLAMES, or fluid-attenuated inversion recovery-hyperintense lesions in anti-myelin oligodendrocyte glycoprotein (anti-myelin oligodendrocyte glycoprotein)-associated encephalitis with seizures, represents a rarely documented syndrome characterized by ambiguous features. Positioned within the spectrum of inflammatory demyelinating diseases of the central nervous system, it is regarded as a distinct subset of myelin oligodendrocyte glycoprotein antibody-associated disease, the latest classification in this domain. Myelin oligodendrocyte glycoprotein antibody-associated disease exhibits a diverse clinical spectrum, spanning from solitary optic neuritis or myelitis to multifocal central nervous system demyelination, manifesting as acute disseminated encephalomyelitis, or cortical encephalitis accompanied by seizures, delineating the fluid-attenuated inversion recovery-hyperintense lesions in anti-myelin oligodendrocyte glycoprotein-associated encephalitis with seizures syndrome. We present a compelling case study of a 30-year-old individual with a history of recurrent seizures initially diagnosed with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes. However, the disease's progression more closely resembled self-resolving cerebral cortical encephalitis linked with myelin oligodendrocyte glycoprotein antibodies. In addition, we undertake a systematic review of literature cases to explore the diagnostic significance of magnetic resonance angiography, fluid-attenuated inversion recovery, and specialized markers such as diffusion-weighted imaging and perfusion in discerning fluid-attenuated inversion recovery-hyperintense lesions in anti-myelin oligodendrocyte glycoprotein-associated encephalitis with seizures syndrome and elucidating its distinctive characteristics.
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页数:8
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