Complete remission of Schnitzler syndrome and Waldenström macroglobulinemia under rituximab-cyclophosphamide-dexamethasone

Dermatology. 2015;230(1):18-22. doi: 10.1159/000368349. Epub 2014 Nov 27.

Abstract

In Schnitzler syndrome, which is mostly diagnosed with a low and asymptomatic monoclonal peak, anakinra has always exhibited a complete but only transient control of the auto-inflammatory signs, which are induced by interleukin (IL)-1 auto-activation. We focused on the treatment of a case of Schnitzler syndrome with moderate macroglobulinemia peak. Anakinra failed to improve the severe inflammatory anaemia and the dysglobulinemia, but rituximab-dexamethasone-cyclophosphamide chemotherapy alone allowed a complete response. The correlation between the clinical, pro-inflammatory cytokines and dysglobulinemia complete controls with chemotherapy proves the following: (1) the dual action of this treatment in both the auto-inflammatory and dysglobulinemia components of the syndrome and (2) a different but entangled cytokine network in the pathogenesis of the auto-inflammatory and dysglobulinemia components of the syndrome.

Publication types

  • Case Reports

MeSH terms

  • Antibodies, Monoclonal, Murine-Derived / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Cyclophosphamide / administration & dosage
  • Dexamethasone / administration & dosage
  • Female
  • Humans
  • Interleukin 1 Receptor Antagonist Protein / therapeutic use
  • Middle Aged
  • Remission Induction
  • Rituximab
  • Schnitzler Syndrome / drug therapy*
  • Waldenstrom Macroglobulinemia / drug therapy*

Substances

  • Antibodies, Monoclonal, Murine-Derived
  • Interleukin 1 Receptor Antagonist Protein
  • Rituximab
  • Dexamethasone
  • Cyclophosphamide