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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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Posterior reversible encephalopathy in a GT1a positive oculopharyngeal variant of Guillain-Barré syndrome: A case-report and review of the literature

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Auteur
Xiromerisiou G., Kalampokini S., Rikos D., Provatas A., Tsouris Z., Markou K., Ralli S., Dardiotis E.
Date
2020
Language
en
DOI
10.1016/j.clineuro.2020.106037
Sujet
ganglioside antibody
ganglioside GD 1a
ganglioside GD 1b
ganglioside GD3
ganglioside GM1 antibody
ganglioside GM1b antibody
ganglioside GM2 antibody
ganglioside GQ 1b antibody
ganglioside GT 1a
ganglioside GT 1b
immunoglobulin
immunoglobulin G antibody
immunoglobulin M antibody
labetalol
nitroprusside sodium
sulfatide
unclassified drug
ganglioside
immunoglobulin
adult
case report
cerebrospinal fluid analysis
clinical article
computer assisted tomography
confusion
diplopia
dysarthria
dysautonomia
dysphagia
female
follow up
Guillain Barre syndrome
hallucination
headache
human
hypertension
malignant hypertension
neuroimaging
neurologic examination
oculopharyngeal variant of Guillain Barre syndrome
orthostatic hypotension
posterior reversible encephalopathy syndrome
ptosis (eyelid)
Review
thin layer chromatography
tongue
weakness
complication
dysautonomia
Guillain Barre syndrome
immunology
posterior reversible encephalopathy syndrome
Adult
Female
Gangliosides
Guillain-Barre Syndrome
Humans
Immunoglobulins, Intravenous
Posterior Leukoencephalopathy Syndrome
Primary Dysautonomias
Elsevier B.V.
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Résumé
Guillain-Barre syndrome (GBS) is the most common cause of acute flaccid paralysis and its incidence increases with age, although all age groups can be affected. The cranial subtypes of GBS account for approximately 5% of cases. Posterior reversible encephalopathy syndrome (PRES) is an acute neurological disorder, mostly reversible but with increased morbidity with permanent neurological sequelae in severe cases. The coexistence of these two syndromes is very rare and underdiagnosed. To the best of our knowledge, there are several dozen cases reported in the literature including ours with the coexistence of these two syndromes in adult patients. We present a rare case of oculopharyngeal type of GBS followed by PRES syndrome. Based on the reviewed cases we discuss various pathogenic mechanisms that support the association between these two entities. This review illustrates the importance of detecting PRES syndrome in the context of acute inflammatory immune-mediated polyneuropathies especially when the patients present early dysautonomia. We also discuss the importance of early administration of immunoglobulin (IVIG) treatment but the possible risks that poses to the occurrence of PRES syndrome as well. © 2020 Elsevier B.V.
URI
http://hdl.handle.net/11615/80855
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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