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Prolonged remission of SLE-associated polyradiculoneuropathy after a single course of intravenous immunoglobulin.

Abstract
Polyradiculoneuropathy is a rare and potentially severe complication of systemic lupus erythematosus (SLE). Treatment is not codified and response to corticosteroid is inconstant. We report the case of a patient with severe SLE-associated polyradiculoneuropathy and autoimmune thrombocytopenia. Dramatic neurologic improvement and correction of thrombocytopenia were observed after a single course of high-dose intravenous immunoglobulin infusions (IVIg, 2g/kg body weight). Our case suggests that IVIg may be effective in the treatment of this unusual condition.
AuthorsP Lesprit, F Mouloud, P Bierling, A Schaeffer, P Cesaro, C Brun-Buisson, B Godeau
JournalScandinavian journal of rheumatology (Scand J Rheumatol) Vol. 25 Issue 3 Pg. 177-9 ( 1996) ISSN: 0300-9742 [Print] England
PMID8668963 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Immunoglobulins, Intravenous
Topics
  • Aged
  • Aged, 80 and over
  • Humans
  • Immunoglobulins, Intravenous (administration & dosage)
  • Lupus Erythematosus, Systemic (complications)
  • Male
  • Polyradiculoneuropathy (complications, therapy)
  • Purpura, Thrombocytopenic, Idiopathic (complications, therapy)
  • Remission Induction
  • Time Factors

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