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Severe headache in primary Sjögren’s syndrome treated with intrathecal rituximab

A severe and persistent migrainous headache in a patient with primary Sjøgren's syndrome unresponsive to treatment with immunosuppressive drugs, triptans, opioids, and NSAIDs, responded successfully to intrathecal B‐cell depletion with rituximab. We hypothesize that brain‐resident autoreactive...

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Detalles Bibliográficos
Autores principales: Tjensvoll, Anne Bolette, Lauvsnes, Maria Boge, Norheim, Katrine Brekke, Omdal, Roald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406134/
https://www.ncbi.nlm.nih.gov/pubmed/30899462
http://dx.doi.org/10.1002/ccr3.1987
Descripción
Sumario:A severe and persistent migrainous headache in a patient with primary Sjøgren's syndrome unresponsive to treatment with immunosuppressive drugs, triptans, opioids, and NSAIDs, responded successfully to intrathecal B‐cell depletion with rituximab. We hypothesize that brain‐resident autoreactive B cells were involved in headache pathogenesis and were eliminated by this procedure.