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Anti-GAD Antibodies as an Etiology of Cerebral Cortical Encephalitis: 2 Case Reports
Bruno Lemarchant1,2, Cristina Birzu3, Louis Cousyn4,5
1Department of Neurology, Centre de Compétence Maladies Rares (CCMR) Syndrome Neurologique Paranéoplasique-Encéphalites Auto-Immunes (SNP-EA), CHU of Lille, Lille, France.
Introduction:
Cerebral cortical encephalitis (CCE) has been recently described as an entity associated with anti-MOG antibodies and, in some cases, of anti-GABAAR 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-GABAAR 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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