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...
Uložené v:
| Vydané v: | Case reports in neurological medicine Ročník 2025; číslo 1; s. 5686302 |
|---|---|
| Hlavní autori: | , , , |
| 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!
|
| 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 |