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Rituximab in a childhood-onset idiopathic refractory chronic inflammatory demyelinating polyneuropathy.

Abstract
Childhood-onset chronic inflammatory demyelinating polyneuropathy (CIDP) are generally responsive to conventional immunosuppressant treatments. However about 20% of patients may be refractory to several treatments and the disease has poor outcome. Rituximab is becoming a promising treatment in selected adult cases of severe CIDPs. We report the effectiveness of Rituximab in a refractory childhood-onset CIDP and we suggest this treatment as an effective choice in unresponsive childhood CIDP.
AuthorsAdele D'Amico, Michela Catteruccia, Fabrizio De Benedetti, Marina Vivarelli, Manuela Colucci, Simona Cascioli, Enrico Bertini
JournalEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society (Eur J Paediatr Neurol) Vol. 16 Issue 3 Pg. 301-3 (May 2012) ISSN: 1532-2130 [Electronic] England
PMID21903431 (Publication Type: Case Reports, Journal Article)
CopyrightCopyright © 2011 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
Chemical References
  • Antibodies, Monoclonal, Murine-Derived
  • Immunologic Factors
  • Rituximab
Topics
  • Age of Onset
  • Antibodies, Monoclonal, Murine-Derived (therapeutic use)
  • Child
  • Electrophysiology
  • Female
  • Humans
  • Immunologic Factors (therapeutic use)
  • Polyradiculoneuropathy, Chronic Inflammatory Demyelinating (drug therapy, physiopathology)
  • Rituximab
  • Young Adult

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