Progressive myelin oligodendrocyte glycoprotein-associated demyelination mimicking leukodystrophy.


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
08 2022
Historique:
pubmed: 24 6 2022
medline: 8 7 2022
entrez: 23 6 2022
Statut: ppublish

Résumé

Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) may be associated with relapsing disease, but clinical progression independent of relapse activity is rare. To report progressive disease in a patient with MOGAD. A single retrospective case report. At 4 years of age, the patient had a single episode of acute disseminated encephalomyelitis. She remained well until age 17 years but over the next 9 years developed progressive spastic quadriparesis, cognitive and bulbar dysfunction. Brain imaging showed a leukodystrophy-like pattern of white matter abnormality with contrast enhancement at different time points. Myelin oligodendrocyte glycoprotein (MOG)-IgG was repeatedly positive by live cell-based assay. Secondary progression may be a rare presentation of MOG-IgG-associated disease.

Sections du résumé

BACKGROUND
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) may be associated with relapsing disease, but clinical progression independent of relapse activity is rare.
OBJECTIVES
To report progressive disease in a patient with MOGAD.
METHODS
A single retrospective case report.
RESULTS
At 4 years of age, the patient had a single episode of acute disseminated encephalomyelitis. She remained well until age 17 years but over the next 9 years developed progressive spastic quadriparesis, cognitive and bulbar dysfunction. Brain imaging showed a leukodystrophy-like pattern of white matter abnormality with contrast enhancement at different time points. Myelin oligodendrocyte glycoprotein (MOG)-IgG was repeatedly positive by live cell-based assay.
CONCLUSION
Secondary progression may be a rare presentation of MOG-IgG-associated disease.

Identifiants

pubmed: 35735077
doi: 10.1177/13524585221090737
doi:

Substances chimiques

Aquaporin 4 0
Autoantibodies 0
Immunoglobulin G 0
Myelin-Oligodendrocyte Glycoprotein 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1481-1484

Commentaires et corrections

Type : CommentIn

Auteurs

Emily Gibbons (E)

National Neuromyelitis Optica Spectrum Disorders Service, The Walton Centre NHS Foundation Trust, Liverpool, UK.

Daniel Whittam (D)

Department of Neurology, Salford Royal NHS Foundation Trust, Salford, UK.

Kariem Elhadd (K)

National Neuromyelitis Optica Spectrum Disorders Service, The Walton Centre NHS Foundation Trust, Liverpool, UK.

Maneesh Bhojak (M)

National Neuromyelitis Optica Spectrum Disorders Service, The Walton Centre NHS Foundation Trust, Liverpool, UK.

Nitika Rathi (N)

Department of Neuropathology, The Walton Centre NHS Foundation Trust, Liverpool, UK.

Shivaram Avula (S)

Department of Radiology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.

Anu Jacob (A)

National Neuromyelitis Optica Spectrum Disorders Service, The Walton Centre NHS Foundation Trust, Liverpool, UK/Cleveland Clinic, Abu Dhabi, United Arab Emirates.

Michael Griffiths (M)

Department of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, UK/National Institute for Health Research, Health Protection Research Unit on Emerging and Zoonotic Infections, University of Liverpool, UK/Department of Neurology, Alderhey Children's NHS Foundation Trust, Liverpool, UK.

Saif Huda (S)

National Neuromyelitis Optica Spectrum Disorders Service, The Walton Centre NHS Foundation Trust, Liverpool, UK.

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Classifications MeSH