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Neuromyelitis optica spectrum disorder with AQP4‐IgG presenting as area postrema syndrome and progressing to myelitis: A rare case report

KEY CLINICAL MESSAGE: Neuromyelitis optica spectrum disorders can less commonly present with area postrema syndrome progressing to myelitis. Management involves intravenous glucocorticoids, plasma exchange, and preventive immunotherapy. ABSTRACT: Neuromyelitis optica spectrum disorders can less comm...

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Detalles Bibliográficos
Autores principales: Jagannath, Preethi, K, Mohammed Suhail, S, Shaikh Mohammed Aslam, Kulkarni, Ashwin, Prashanth, Polasu Sri Satya Sai, Madan, Hritik, Anand, Ayush
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319961/
https://www.ncbi.nlm.nih.gov/pubmed/37415585
http://dx.doi.org/10.1002/ccr3.7636
Descripción
Sumario:KEY CLINICAL MESSAGE: Neuromyelitis optica spectrum disorders can less commonly present with area postrema syndrome progressing to myelitis. Management involves intravenous glucocorticoids, plasma exchange, and preventive immunotherapy. ABSTRACT: Neuromyelitis optica spectrum disorders can less commonly present with area postrema syndrome progressing to myelitis. The majority of patients have positive AQP4‐Ab. Diagnosis is based on clinical and imaging findings. These patients can be treated with intravenous glucocorticoids, plasma exchange, and preventive immunotherapy.