Eur J Neurol
Department of Neuro-Oncology, Institut, du Cerveau, National Referent Center for Paraneoplastic and Autoimmune Encephalitis (SNP-EA), Sorbonne Université, Hôpital La Pitié Salpêtrière, Paris, France.
Published: March 2025
Introduction: Cerebral cortical encephalitis (CCE) has been recently described as an entity associated with anti-MOG antibodies and, in some cases, of anti-GABAR encephalitis. No clear association with other antibodies has been reported to date. We describe two cases of patients presenting clinical and radiological features of diffuse cortical encephalitis associated with anti-GAD antibodies.
Method: In two patients with CCE, screening for the presence of anti-GAD and other antibodies was performed, along with a complete workup for alternative diagnoses.
Results: Two patients showing clinical and radiological features of CCE were tested positive for anti-GAD antibodies. MRI scan revealed multiple bilateral areas of cortico-subcortical FLAIR hyperintensities. They were both tested negative for anti-MOG, anti-NMDAr, and anti-GABAR antibodies. An ovarian teratoma was discovered in patient 1. Clinical and radiological evolution was favorable in both patients after cumulated therapies in the acute phase.
Discussion: CCE could be a new manifestation of anti-GAD antibodies, with distinct features compared to anti-MOG antibodies related to CCE. We recommend screening for anti-GAD antibodies in the context of CCE, especially in case of atypical features for MOG antibodies-associated disease (MOGAD).
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http://dx.doi.org/10.1111/ene.70096 | DOI Listing |
Eur J Neurol
March 2025
Department of Neuro-Oncology, Institut, du Cerveau, National Referent Center for Paraneoplastic and Autoimmune Encephalitis (SNP-EA), Sorbonne Université, Hôpital La Pitié Salpêtrière, Paris, France.
Introduction: Cerebral cortical encephalitis (CCE) has been recently described as an entity associated with anti-MOG antibodies and, in some cases, of anti-GABAR encephalitis. No clear association with other antibodies has been reported to date. We describe two cases of patients presenting clinical and radiological features of diffuse cortical encephalitis associated with anti-GAD antibodies.
View Article and Find Full Text PDFCureus
January 2025
Department of Nervous Diseases and Neurosurgery, Faculty of Therapeutics, A.Ya. Kozhevnikov Clinic of Nervous System Diseases, University Clinical Hospital No. 3, I.M. Sechenov First Moscow State Medical University, Moscow, RUS.
Vertigo is a common symptom encountered by neurologists in clinical practice. Position-dependent vertigo can occur at the onset of autoimmune encephalitis, often being misinterpreted as benign paroxysmal positional vertigo (BPPV). This study describes a clinical case of a patient with autoimmune encephalitis associated with GAD65 antibodies, who initially presented with systemic positional vertigo.
View Article and Find Full Text PDFInt Med Case Rep J
January 2025
Department of Neurology, Changhai Hospital, Naval Medical University (Second Military Medical University), Shanghai, People's Republic of China.
Background: Coexistence of autoimmune encephalitis (AE) with multiple autoantibodies is of particular concern because overlying antibodies may cause variation of clinical manifestations. Coexistence of anti-glutamic acid decarboxylase (GAD) and anti-Gamma-aminobutyric acid-α-receptor (GABAAR) antibodies in AE was rare.
Case Presentation: A 44-year-old female patient presented to our hospital due to cognitive decline for 4 years, seizures, slowed speech and depression for 2 months.
Front Immunol
January 2025
Department of Neurology, The First Affiliated Hospital of Anhui University of Traditional, Chinese Medicine, Hefei, Anhui, China.
Autoimmune polyendocrine syndromes (APS) is a rare group of disorders caused by impaired function of multiple endocrine glands due to disruption of immune tolerance. Of which, type 2 (APS-2) is the most common. Glutamic acid decarboxylase (GAD) is the rate-limiting enzyme for the synthesis of gamma-aminobutyric acid (GABA).
View Article and Find Full Text PDFCureus
December 2024
Neurology, Tecnológico de Monterrey, Monterrey, MEX.
Isolated ophthalmoplegia as an anti-glutamic acid decarboxylase 65 (anti-GAD65) antibody-associated neurological syndrome is rare. We present a case of a 22-year-old pregnant Hispanic female patient who presented initially with a left oculomotor nerve palsy following an emergency department (ED) visit for migraine headache. Brain imaging was done with no important findings.
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