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...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:Case reports in neurological medicine Ročník 2025; číslo 1; s. 5686302
Hlavní autori: Huang, Yunchen, Song, Yafei, Liu, Ding, Liu, Yin
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States John Wiley & Sons, Inc 01.01.2025
Wiley
Predmet:
ISSN:2090-6668, 2090-6676
On-line prístup:Získať plný text
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Popis
Shrnutí: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.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Case Study-2
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:2090-6668
2090-6676
DOI:10.1155/crnm/5686302