Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2022 Oct 19;9(6):e200020.
doi: 10.1212/NXI.0000000000200020. Print 2022 Nov.

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Presenting as Intracranial Hypertension: A Case Report

Affiliations
Case Reports

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Presenting as Intracranial Hypertension: A Case Report

Jaydip Ray Chaudhuri et al. Neurol Neuroimmunol Neuroinflamm. .

Abstract

The production of autoantibodies against myelin oligodendrocyte glycoprotein (MOG) can cause a spectrum of autoimmune disorders, including optic neuritis, transverse myelitis, brainstem encephalitis, and acute disseminated encephalomyelitis. In this study, we present the case of a 19-year-old woman with an unusual clinical presentation of intracranial hypertension (IH) and bilateral papilledema. The patient presented with symptoms of increased intracranial pressure, which followed a relapsing, remitting course over several months. Serial CSF studies showed an increased opening pressure during clinical relapses. The CSF and serum tested positive for MOG immunoglobulin G antibodies. Contrast-enhanced MRI of the brain showed mild meningeal enhancement in the left parietal region with subtle underlying cortical hyperintensities, indicating possible fluid-attenuated inversion recovery variable unilateral enhancement of the leptomeninges. The patient responded well to immunosuppressive therapy using rituximab. The presentation of MOG antibody-associated disease (MOGAD) as IH without optic neuritis is rare. This report presents the first description of a relapsing remitting course presenting each time with only symptoms of raised intracranial pressure, without developing any typical clinical manifestations of MOGAD.

PubMed Disclaimer

Figures

Figure 1
Figure 1. MRI Brain FLAIR and Contrast
(A) Abnormal leptomeningeal enhancement along the left temporoparietal cortical sulci. (B) Fluid-attenuated inversion recovery (FLAIR) image showing minimal hyperintensity of the adjoining cortex.
Figure 2
Figure 2. Flowchart of the Clinical Course of Patient Treatment
MMF = mycophenolate mofetil; MOG = myelin oligodendrocyte glycoprotein.

References

    1. Waters PJ, Komorowski L, Woodhall M, et al. . A multicenter comparison of MOG-IgG cell-based assays. Neurology. 2019;92(11):e1250-e1255. - PMC - PubMed
    1. Netravati M, Holla VV, Nalini A, et al. . Myelin oligodendrocyte glycoprotein-antibody-associated disorder: a new inflammatory CNS demyelinating disorder. J Neurol. 2021;268(4):1419-1433. - PubMed
    1. Hacohen Y, Rossor T, Mankad K, et al. . ‘Leukodystrophy-like’ phenotype in children with myelin oligodendrocyte glycoprotein antibody-associated disease. Dev Med Child Neurol. 2018;60(4):417-423. - PubMed
    1. Corbett J, Bhuta S, Prain K, Brilot F, Sabet A, Broadley SA. PRES-like presentation in MOG antibody-related demyelination (MARD). J Clin Neurosci. 2020;72:453-455. - PubMed
    1. Narayan RN, Wang C, Sguigna P, Husari K, Greenberg B. Atypical Anti-MOG syndrome with aseptic meningoencephalitis and pseudotumor cerebri-like presentations. Mult Scler Relat Disord. 2019;27:30-33. - PubMed

Publication types