Relapsing lumbosacral myeloradiculitis: An unusual presentation of MOG antibody disease.
Autoantibodies
Autoimmune Diseases of the Nervous System
/ complications
Demyelinating Diseases
/ complications
Diagnosis, Differential
Humans
Lumbar Vertebrae
Magnetic Resonance Imaging
Male
Middle Aged
Myelin-Oligodendrocyte Glycoprotein
/ immunology
Myelitis
/ diagnosis
Radiculopathy
/ diagnosis
Recurrence
Sacrum
MOG antibody
cauda equina enhancement
demyelination
lumbosacral myeloradiculitis
relapsing
Journal
Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185
Informations de publication
Date de publication:
04 2020
04 2020
Historique:
pubmed:
2
4
2019
medline:
8
5
2021
entrez:
2
4
2019
Statut:
ppublish
Résumé
Myelin oligodendrocyte glycoprotein antibody (MOG-Ab) seropositivity is being increasingly reported in diverse demyelinating syndromes with monophasic and relapsing presentations. Conus myelitis is described as a typical feature of MOG-Ab seropositivity. However, the association with lumbosacral radiculitis in this disease is not well-recognized. Here, we report a patient with relapsing MOG-Ab disease who presented clinically and radiologically with a relapsing lumbosacral myeloradiculopathy. This presentation raises the diagnostic possibilities of chronic infections, sarcoidosis, and neoplastic infiltration. This case illustrates the need to consider MOG-Ab disease as one of the differential diagnosis for a non-compressive lumbosacral myeloradiculopathy.
Identifiants
pubmed: 30931808
doi: 10.1177/1352458519840747
doi:
Substances chimiques
Autoantibodies
0
MOG protein, human
0
Myelin-Oligodendrocyte Glycoprotein
0
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
509-511Commentaires et corrections
Type : CommentIn