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Co-occurrence of MS and ALS: a clue in favor of common pathophysiological findings?
Guennoc, Anne-Marie; Pallix-Guyot, Maud; Le Page, Emmanuelle; Le Port, Damien; Daryabin, Mathieu; Hergesheimer, Rudolph; Beltran, Stéphane; Tourbah, Ayman; Edan, Gilles; Corcia, Philippe.
Afiliación
  • Guennoc AM; a Neurology Department , University Hospital Center of Tours , Tours , France.
  • Pallix-Guyot M; b Neurology Department , Regional Hospital Center of Orléans , Orléans , France.
  • Le Page E; c Neurology Department , University Hospital Center of Rennes , Rennes , France.
  • Le Port D; c Neurology Department , University Hospital Center of Rennes , Rennes , France.
  • Daryabin M; d Neurology Department , Hospital Center of Angoulême , Angoulême , France.
  • Hergesheimer R; a Neurology Department , University Hospital Center of Tours , Tours , France.
  • Beltran S; a Neurology Department , University Hospital Center of Tours , Tours , France.
  • Tourbah A; e ALS Center, University Hospital Center of Tours , Tours , France , and.
  • Edan G; f Neurology Department , University Hospital Center of Reims , Reims , France.
  • Corcia P; c Neurology Department , University Hospital Center of Rennes , Rennes , France.
Article en En | MEDLINE | ID: mdl-30175630
ABSTRACT
Amyotrophic lateral sclerosis (ALS) and multiple sclerosis (MS) are two neurological disorders that seem, theoretically, completely divergent according to epidemiological, clinical, pathophysiological, and therapeutic data. However, some reports that have mentioned the occurrence of both conditions within the same patient underpin the suggestion that this co-occurrence might not be random. We report six co-occurrences of ALS and MS cases, focusing on epidemiological and clinical diseases findings. We then compare our cohort to those in the literature. Our cohort was composed of five females and one male. The age of onset for MS ranged from 27 to 54 years with either primary or secondary prominence while all being progressive. Both diseases occurred sequentially in all but one the cases. Concerning ALS, the age of onset ranged from 51 to 60 years and the site of onset was the legs in 5/6 cases. The disease lasted from four to 29 months. Although infrequent, this co-occurrence supports the hypothesis of common, pathophysiological mechanisms between ALS and MS. We discuss some arguments favoring a potential link between both conditions.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Esclerosis Amiotrófica Lateral / Esclerosis Múltiple Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Amyotroph Lateral Scler Frontotemporal Degener Año: 2018 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Esclerosis Amiotrófica Lateral / Esclerosis Múltiple Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Amyotroph Lateral Scler Frontotemporal Degener Año: 2018 Tipo del documento: Article País de afiliación: Francia