Pachymeningitis With Dural Vessel Dilatation in MOG Antibody–Associated Disease: A Case Report

Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is a novel inflammatory demyelinating disorder marked by heterogenous clinical and radiological manifestations. Pachymeningitis is a rare manifestation. An 18-year-old male was hospitalized with fever, dizziness, altered c...

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Veröffentlicht in:Case reports in neurological medicine Jg. 2025; H. 1; S. 5686302
Hauptverfasser: Huang, Yunchen, Song, Yafei, Liu, Ding, Liu, Yin
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States John Wiley & Sons, Inc 01.01.2025
Wiley
Schlagworte:
Antibodies
Blood
Bone marrow
Case reports
Cellular biology
Cerebrospinal fluid
Consciousness
Convulsions & seizures
Diagnostic tests
Disease
Diseases
Encephalitis
Glycoproteins
Hypotension
Leukocytes
Levetiracetam
Magnetic resonance imaging
Meningitis
Myelin proteins
Nervous system
Neutrophils
Seizures (Medicine)
Viral antibodies
seizure
dural
myelin oligodendrocyte glycoprotein
meningitis
ISSN:2090-6668, 2090-6676
Online-Zugang:Volltext
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Zusammenfassung:Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is a novel inflammatory demyelinating disorder marked by heterogenous clinical and radiological manifestations. Pachymeningitis is a rare manifestation. An 18-year-old male was hospitalized with fever, dizziness, altered consciousness, and seizure attacks. Serum testing was positive for MOG antibodies. Diffuse pachymeningitis with prominent dural vessel dilation was observed prior to treatment, which markedly improved after hormone therapy. MOGAD pachymeningitis with dural vessel dilatation broadens the imaging spectrum of MOGAD.
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ISSN:2090-6668
2090-6676
DOI:10.1155/crnm/5686302