Atypical Alterations of cerebrospinal fluid in Guillain Barré Syndrome: Cases Reports.
- Laura Zelada-Riós,
- Erik Guevara-Silva(corresponding author),
- ,
- César Caparó-Zamalloa,
- Mariá Meza-Vega
- docencia y atención especializada en epilepsia,
- ,
- University of California, San Francisco,
- Department of Neurology
Open access
Publication Information
Output type
Original language
SpanishPages 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
ISSN
0034-8597Publication 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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