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Rituximab and intravenous immunoglobulins for relapsing postinfectious opsoclonus-myoclonus syndrome.

Abstract
We describe 2 children with postinfectious opsoclonus-myoclonus syndrome. Although the patients initially responded to monotherapy with methylprednisolone, intravenous immunoglobulins, or rituximab, they manifested persistent neurologic deficits and relapsing signs. Treatment with rituximab in combination with intravenous immunoglobulin, however, resulted in significant longterm clinical improvement.
AuthorsWilhelmina G Leen, Corry M Weemaes, Marcel M Verbeek, Michèl A Willemsen, Jan J Rotteveel
JournalPediatric neurology (Pediatr Neurol) Vol. 39 Issue 3 Pg. 213-7 (Sep 2008) ISSN: 0887-8994 [Print] United States
PMID18725071 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Immunoglobulins, Intravenous
  • Immunologic Factors
  • Rituximab
Topics
  • Antibodies, Monoclonal (administration & dosage, therapeutic use)
  • Antibodies, Monoclonal, Murine-Derived
  • Drug Therapy, Combination
  • Female
  • Humans
  • Immunoglobulins, Intravenous (administration & dosage, therapeutic use)
  • Immunologic Factors (administration & dosage, therapeutic use)
  • Infant
  • Opsoclonus-Myoclonus Syndrome (drug therapy, pathology)
  • Recurrence
  • Rituximab
  • Treatment Outcome

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