Anti-γ-aminobutyric acid-A receptor encephalitis with refractory seizures and cognitive impairment in a young woman: A case report

Anti-γ-aminobutyric acid-A receptor (GABA A R) encephalitis is an underappreciated cause of autoimmune encephalitis and remains refractory to antiepileptic therapies unless autoimmune responses are addressed. Herein, we reported a case of anti-GABA A R encephalitis in a young woman. A 29-year-old wo...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in neurology Vol. 13
Main Authors: Yang, Xue, Deng, Bo, Wang, Shengjun, Wang, Xiaotang, Cao, Lili, Chen, Xiangjun, Zhao, Xiuhe
Format: Journal Article
Language:English
Published: Frontiers Media S.A 29-08-2022
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Anti-γ-aminobutyric acid-A receptor (GABA A R) encephalitis is an underappreciated cause of autoimmune encephalitis and remains refractory to antiepileptic therapies unless autoimmune responses are addressed. Herein, we reported a case of anti-GABA A R encephalitis in a young woman. A 29-year-old woman was admitted because of seizures for 10 months, memory decline for 7 months, and paroxysmal limbs jerking for 5 months. At admission, the patient showed mild cognitive impairment. Cell-based assays found no antibodies associated with common autoimmune encephalitis in the cerebrospinal fluid (CSF) and no antibodies in the plasma and CSF against central nervous system demyelination-associated proteins. MRI revealed multiple cortical-subcortical abnormalities and electroencephalography demonstrated periodic epileptiform discharges during paroxysmal clonus. A second test 1 month after admission detected antibodies against GABA A R α1/β3/γ2 in the plasma and CSF, leading to a diagnosis of anti-GABA A R encephalitis. The patient received intravenous immunoglobulin, prednisone, azathioprine, and levetiracetam and recovered from limb jerks and was no longer amnesic. A second episode occurred after an apparent cold and was managed by intravenous immunoglobulin, cyclophosphamide, and methylprednisolone with subsequent prednisone and levetiracetam. The patient was able to speak and ambulate after 15 days of treatment. Her MMSE, MoCA, and MRS scores improved. Physicians should harbor a high index of suspicion of anti-GABA A R encephalitis in refractory encephalitis patients with the manifestation of seizures or psychiatric disorders. Tests for a comprehensive panel of antibodies associated with anti-GABA A R encephalitis should be carried out in suspected cases and immunotherapy should be promptly initiated upon diagnosis to prevent irreversible neurological damage.
Bibliography:Reviewed by: Suvasini Sharma, University of Delhi, India; Anne-Marie Landtblom, Uppsala University, Sweden; Masayuki Tahara, Utano Hospital (NHO), Japan
This article was submitted to Multiple Sclerosis and Neuroimmunology, a section of the journal Frontiers in Neurology
Edited by: Hans-Peter Hartung, Heinrich Heine University of Düsseldorf, Germany
ISSN:1664-2295
1664-2295
DOI:10.3389/fneur.2022.954494