Idiopathic dysautonomia treated with intravenous gammaglobulin.
Autor(es): Heafield M. T.; Gammage M. D.; Nightingale S.; Williams A. C.
Resumo: A previously healthy 23-year-old man presented with a short history of abdominal pain and diarrhoea followed by blurred vision, severe postural hypotension, reduced sweating and unremitting fever. Examination revealed fixed dilated pupils, impaired sweating and postural hypotension. Clinical and neurophysiological examination showed no motor or sensory deficit. A diagnosis of idiopathic autonomic neuropathy was made. He became gravely ill with profound life-threatening hypotension and a prolonged ileus. Within 36 h of receiving intravenous gammaglobulin (IVGG) his pupillary areflexia and severe hypotension resolved. 2 weeks later the autonomic failure recurred but again responded to treatment with IVGG. IVGG is a recognised treatment for Guillain-Barré syndrome. This case report demonstrates that IVGG is also effective in the rare pure dysautonomic variant.
Imprenta: Lancet, v. 347, n. 8993, p. 28-29, 1996
Identificador do objeto digital: 10.1016/S0140-6736(96)91559-7
Descritores: Guillain-Barre Syndrome - Proteins ; Guillain-Barre Syndrome - Antibodies ; Guillain-Barre Syndrome - Clinical examination
Data de publicação: 1996
