Guillain-Barré syndrome and its variants: a case of acute motor-sensory axonal neuropathy in Jamaica.
Autor(es)Fletcher-Peddie K.; Alfred R.; Penn-Brown K.; Gayle F.; Gilbert D. T.; Elliot V.; Ferguson T. S.
ResumoThis paper reports a case of a Jamaican young woman who experienced flaccid quadriparesis and bulbar weakness over a three-week period after a gastrointestinal illness. Nerve conduction studies confirmed an axonal type neuropathy consistent with the acute motor-sensory axonal neuropathy variant of the Guillain-Barré syndrome. Recovery, although evident, was slow and was augmented after a course of intravenous immunoglobulin. The patient was discharged from hospital after three months but was re-admitted one week later and eventually succumbed to complications of the illness. This case serves as a reminder that Guillain-Barré syndrome is now the most common cause of acute flaccid paralysis and should be considered early in all patients presenting with flaccid quadriparesis.
ImprentaThe West Indian Medical Journal, v. 62, n. 7, p. 658-666, 2013
Identificador do Objeto Digital10.7727/wimj.2013.039
DescritoresGuillain-Barre Syndrome - Pathogenesis ; Guillain-Barre Syndrome - Proteins ; Guillain-Barre Syndrome - Antibodies ; Guillain-Barre Syndrome - Epidemiology ; Guillain-Barre Syndrome - Public health
Data de Publicação:2013