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Guillain-Barré syndrome in association with antitumour necrosis factor therapy: a case of mistaken identity.
Patwala, Kurvi; Crump, Nicholas; De Cruz, Peter.
Afiliación
  • Patwala K; Department of Gastroenterology, Austin Health, Heidelberg, Australia.
  • Crump N; Department of Neurology, Austin Health, Heidelberg, Australia.
  • De Cruz P; Department of Gastroenterology, Austin Health, Heidelberg, Australia.
BMJ Case Rep ; 20172017 Jul 05.
Article en En | MEDLINE | ID: mdl-28679512
ABSTRACT
Guillain-Barré syndrome (GBS) is an immune-mediated disease characterised by evolving ascending limb weakness, sensory loss and areflexia. Two-thirds of GBS cases are associated with preceding infection. However, GBS has also been described in association with antitumour necrosis factor (TNF) therapies including infliximab and adalimumab for chronic inflammatory disorders such as rheumatoid arthritis, ankylosing spondylitis and inflammatory bowel disease. We present the case of a patient who developed GBS while undergoing treatment with adalimumab in combination with azathioprine for severe fistulising Crohn's disease, and review the literature on neurological adverse events that occur in association with anti-TNF therapy. We also propose an approach to the optimal management of patients who develop debilitating neurological sequelae in the setting of anti-TNF therapy.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Azatioprina / Enfermedad de Crohn / Factor de Necrosis Tumoral alfa / Síndrome de Guillain-Barré / Adalimumab / Inmunosupresores / Antiinflamatorios Tipo de estudio: Risk_factors_studies Límite: Adult / Humans / Male Idioma: En Revista: BMJ Case Rep Año: 2017 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Azatioprina / Enfermedad de Crohn / Factor de Necrosis Tumoral alfa / Síndrome de Guillain-Barré / Adalimumab / Inmunosupresores / Antiinflamatorios Tipo de estudio: Risk_factors_studies Límite: Adult / Humans / Male Idioma: En Revista: BMJ Case Rep Año: 2017 Tipo del documento: Article País de afiliación: Australia