Autoimmune glial fibrillary acidic protein astrocytopathy mimics infectious meningitis: Two case reports.

Autoimmune Glial fibrillary acidic protein astrocytopathy Intracranial infection Meningitis

Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 29 04 2020
revised: 07 06 2020
accepted: 30 06 2020
pubmed: 10 7 2020
medline: 15 5 2021
entrez: 10 7 2020
Statut: ppublish

Résumé

Autoimmune glial fibrillary acidic protein astrocytopathy (A-GFAP-A) has been recently characterized as a novel autoimmune central nervous system (CNS) disorder with GFAP antibody as the biomarker. However, nonspecific symptoms of A-GFAP-A contribute to misdiagnosis. The patients presented with initial symptoms of fever, headache, and nuchal rigidity. Case 1 exhibited mild signs of irritability, active tendon reflexes, and dysuria; case 2 had transient loss of consciousness. Cerebrospinal fluid (CSF) revealed lymphocytosis, elevated protein level, and decreased glucose level. Magnetic resonance imaging (MRI) revealed radial gadolinium enhancement perpendicular to the lateral ventricle. Viral meningitis or tubercular meningitis was suspected. However, their inflammatory and pathogenic indicators showed no abnormal changes, and empirical antibiotic and antiviral drugs did not result in remarkable recovery. Subsequently, cases were detected with a strongly positive expression of GFAP antibody in CSF and the symptoms improved dramatically after high-dose methylprednisolone pulse treatment. A-GFAP-A with meningitis-like symptoms could initially masquerade as intracranial infection, and prompt detection of GFAP antibody is essential for differentiation.

Sections du résumé

BACKGROUND BACKGROUND
Autoimmune glial fibrillary acidic protein astrocytopathy (A-GFAP-A) has been recently characterized as a novel autoimmune central nervous system (CNS) disorder with GFAP antibody as the biomarker. However, nonspecific symptoms of A-GFAP-A contribute to misdiagnosis.
CASE PRESENTATION METHODS
The patients presented with initial symptoms of fever, headache, and nuchal rigidity. Case 1 exhibited mild signs of irritability, active tendon reflexes, and dysuria; case 2 had transient loss of consciousness. Cerebrospinal fluid (CSF) revealed lymphocytosis, elevated protein level, and decreased glucose level. Magnetic resonance imaging (MRI) revealed radial gadolinium enhancement perpendicular to the lateral ventricle. Viral meningitis or tubercular meningitis was suspected. However, their inflammatory and pathogenic indicators showed no abnormal changes, and empirical antibiotic and antiviral drugs did not result in remarkable recovery. Subsequently, cases were detected with a strongly positive expression of GFAP antibody in CSF and the symptoms improved dramatically after high-dose methylprednisolone pulse treatment.
CONCLUSION CONCLUSIONS
A-GFAP-A with meningitis-like symptoms could initially masquerade as intracranial infection, and prompt detection of GFAP antibody is essential for differentiation.

Identifiants

pubmed: 32645637
pii: S2211-0348(20)30425-9
doi: 10.1016/j.msard.2020.102350
pii:
doi:

Substances chimiques

Contrast Media 0
Glial Fibrillary Acidic Protein 0
Gadolinium AU0V1LM3JT

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

102350

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors have declared that no competing interests exist.

Auteurs

Xiao Yang (X)

Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan 75004, China.

Chenyang Zhang (C)

Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan 75004, China.

Jun Zhang (J)

Department of Intensive Care Unit, General Hospital of Ningxia Medical University, Yinchuan 75004, China.

Guisheng Chen (G)

Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan 75004, China.

Li Zhao (L)

Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan 75004, China.

Ping Yang (P)

Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan 75004, China.

Huilu Li (H)

Department of Neurology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China.

Youming Long (Y)

Department of Neurology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China. Electronic address: youminglong@126.com.

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Classifications MeSH