Spinal nerve involvement in early Guillain-Barré syndrome: a clinico-electrophysiological, ultrasonographic and pathological study
Autor(es): Gallardo Elena,Sedano María J,Orizaola Pedro,Sánchez-Juan Pascual,González-Suárez Andrea,García Antonio,Terán-Villagrá Nuria,Ruiz-Soto María,Álvaro Rosa Landeras,Berciano María T,Lafarga Miguel,Berciano José
Resumo: Although prevailing spinal nerve involvement has been recognized in a few detailed Guillain-Barré syndrome (GBS) autopsy reports, imaging studies addressing this question in cervical nerves are lacking. We describe clinical, electrophysiological, ultrasonographic (US) and pathological findings in six consecutive early GBS patients, evaluated within 10 days of onset. Patients' ages ranged from 37 to 80 years. Five patients required mechanical ventilation, two of them having died 9 and 28 days after onset. Upper- and lower-limb nerve US showed abnormal findings in just 8.8% of scanned peripheral nerves. In comparison with 46 aged-matched control subjects, US of the fifth to seventh cervical nerves showed changes in four cases, which consisted of significant nerve enlargement, blurred boundaries of the corresponding ventral rami, or both. Autopsy study in one case demonstrated that pathology, consisting of demyelination and endoneurial inflammatory oedema, mainly involved cervical and lumbar nerves. In early GBS inflammatory oedema of spinal nerves is a pathogenically relevant feature to understanding the mechanism of ascending paralysis, particularly when conventional electrophysiological studies are normal or not diagnostic. Findings advocate the use of cervical nerve US in early GBS.
Palavras-Chave: AIDP; AMAN; AMSAN; Antiganglioside antibody; Axonal degeneration; Demyelination; Electrophysiology; Endoneurial oedema; Experimental allergic neuritis; Guillain-Barré syndrome; Methylprednisolone; Ultrasonography
Imprenta: Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology, v. 126, n. 4, p. 810-819, 2015
Identificador do objeto digital: 10.1016/j.clinph.2014.06.051
Descritores: Guillain-Barre Syndrome - Cell ; Guillain-Barre Syndrome - Cytopathology
Data de publicação: 2015
