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Atypical Alterations of cerebrospinal fluid in Guillain Barré Syndrome: Cases Reports.

Original title: Alteraciones atípicas del líquido cefalorraquídeo en el Síndrome de Guillain-Barré: Reporte de casos.
  • Laura Zelada-Riós
    ,
  • Erik Guevara-Silva(corresponding author)
    ,
  • ,
  • César Caparó-Zamalloa
    ,
  • Mariá Meza-Vega
*Corresponding author for this work
Research Output:
Contribution to journal
Article
Research
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Research
Peer-review

Original language

Spanish

Pages from-to (Number of pages)

Pages 64-68 (5 pages)

Journal (Volume, Issue Number)

Revista de Neuro-Psiquiatria (Volume 84, Issue 1)

Publication milestones

  • Published - 01/2021

Publication status

Published - 01/2021

ISSN

0034-8597

Publication IDs

  • Scopus: 85176892505

Abstract

Guillain-Barré syndrome shows a cyto-albuminologic dissociation in most patients. Pleocytosis or hypoglycorrhachia may defer the diagnosis, a reason for which an infectious etiology must be ruled out. Three cases of Guillain-Barré are described, whose cerebrospinal fluid tests showed limphocytic pleocytosis and persistently elevated protein concentration, while one of the cases also showed hypoglycorrhachia, and the classic cyto-albuminologic dissociation was only demonstrated in subsequent analysis. The neurophysiologic evaluation revealed an axonal disruption in all the patients. The atypical alterations in the context of acute flaccid paralysis warrant a retesting of the cerebrospinal fluid in order to rule out other etiologies, but without postponing the start of treatment.

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