Myelin oligodendrocyte glycoprotein (MOG) antibodies in a patient with glioblastoma: Red flags for false positivity.
Adult
Antibodies, Neoplasm
/ blood
Autoantibodies
/ blood
Autoantigens
/ immunology
Biopsy
Brain Neoplasms
/ blood
Delayed Diagnosis
Diagnostic Errors
Facial Paralysis
/ etiology
False Positive Reactions
Female
Gait Disorders, Neurologic
/ etiology
Glioblastoma
/ blood
Humans
Immunoglobulin G
/ blood
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Myelin-Oligodendrocyte Glycoprotein
/ immunology
Neuroimaging
Paresis
/ etiology
Positron-Emission Tomography
Vertigo
/ etiology
Vision Disorders
/ etiology
Antibody
False positive
Glioblastoma
MOG
Journal
Journal of neuroimmunology
ISSN: 1872-8421
Titre abrégé: J Neuroimmunol
Pays: Netherlands
ID NLM: 8109498
Informations de publication
Date de publication:
15 12 2021
15 12 2021
Historique:
received:
15
08
2021
accepted:
05
09
2021
pubmed:
26
10
2021
medline:
4
1
2022
entrez:
25
10
2021
Statut:
ppublish
Résumé
We present a patient with positive medium titer MOG-IgG and progressive neurological decline whose clinical and radiological phenotype were not consistent with a MOG-IgG associated disorder and ultimately received a diagnosis of glioblastoma after brain biopsy and died 4 weeks later. This represents an important topic with a high frequency of MOG-IgG testing in clinical practice. Due to this there are increasing reports of MOG-IgG positivity in atypical clinical phenotypes, raising the possibility of false positives, which can have important implications. It is important to highlight that judicious clinical evaluation is needed when interpreting MOG-IgG results in atypical settings.
Identifiants
pubmed: 34695769
pii: S0165-5728(21)00270-8
doi: 10.1016/j.jneuroim.2021.577743
pii:
doi:
Substances chimiques
Antibodies, Neoplasm
0
Autoantibodies
0
Autoantigens
0
Immunoglobulin G
0
MOG protein, human
0
Myelin-Oligodendrocyte Glycoprotein
0
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
577743Informations de copyright
Copyright © 2021 Elsevier B.V. All rights reserved.