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A rare case of Miller Fisher variant of Guillain-Barré Syndrome (GBS) induced by a checkpoint inhibitor.
McNeill, Caitlin Jane; Fehmi, Janev; Gladwin, James; Price, Christopher.
Afiliación
  • McNeill CJ; Respiratory, Musgrove Park Hospital, Taunton, UK.
  • Fehmi J; Neurology, Southmead Hospital, Bristol, UK.
  • Gladwin J; Intensive Care, Royal Free Hospital, London, UK.
  • Price C; Neurology, Musgrove Park Hospital, Taunton, UK.
BMJ Case Rep ; 12(8)2019 Aug 13.
Article en En | MEDLINE | ID: mdl-31413049
With the recent development of novel, more potent cancer treatment, in particular, immune 'checkpoint inhibitors', cases of neurological immune-related adverse events are on the rise. Although rare, this includes Guillain-Barré Syndrome (GBS). We present the case of a 68-year-old male who was admitted with sudden onset of worsening neurological symptoms following immunotherapy treatment. These symptoms progressed quickly to respiratory failure requiring intubation and admission to the intensive care unit. He was thoroughly investigated and is believed to have an axonal neuropathy in the form of Miller Fisher Syndrome (MFS) variant of GBS, secondary to immunotherapy treatment. He was initially treated with intravenous immunoglobulin, and later, perhaps more effectively, with high dose steroids which significantly improved his symptoms. This case of checkpoint inhibitor-induced MFS is one of few in the literature and is an important reminder of the potential for new immunotherapeutic agents to cause significant neurotoxic effects. These should be promptly and thoroughly investigated, in particular, as the management of these patients can differ from standard treatments used in these conditions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Miller Fisher / Antineoplásicos Inmunológicos / Nivolumab Tipo de estudio: Diagnostic_studies Límite: Aged / Humans / Male Idioma: En Revista: BMJ Case Rep Año: 2019 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Miller Fisher / Antineoplásicos Inmunológicos / Nivolumab Tipo de estudio: Diagnostic_studies Límite: Aged / Humans / Male Idioma: En Revista: BMJ Case Rep Año: 2019 Tipo del documento: Article Pais de publicación: Reino Unido