Article Dans Une Revue Multiple Sclerosis Journal Année : 2019

Area postrema syndrome: Another feature of anti-GFAP encephalomyelitis

Jonathan Ciron
Fanny Sourdrille
  • Fonction : Auteur
Damien Biotti
Thierry Tchoumi
  • Fonction : Auteur
Raphaël Bernard-Valnet
Nicolas Maubeuge

Résumé

Anti–Glial fibrillary acidic protein (GFAP) encephalomyelitis is a recently described entity and while the spectrum of this disease has been explored, further research is needed to fully describe its phenotype. Area postrema syndrome (APS) is usually associated with neuromyelitis optica spectrum disorders (NMOSDs), whereas no case of APS has been previously reported with anti-GFAP encephalomyelitis. In this article, we report a case of APS in a 41-year-old woman in the context of anti-GFAP encephalomyelitis. This case was not associated with additional anti-AQP4 IgG and therefore extends the clinico-radiological spectrum of anti-GFAP encephalomyelitis.

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Dates et versions

hal-04783515 , version 1 (14-11-2024)

Identifiants

Citer

Jonathan Ciron, Fanny Sourdrille, Damien Biotti, Thierry Tchoumi, Anne Ruiz, et al.. Area postrema syndrome: Another feature of anti-GFAP encephalomyelitis. Multiple Sclerosis Journal, 2019, 26 (2), pp.253-255. ⟨10.1177/1352458518817992⟩. ⟨hal-04783515⟩
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