Successful methotrexate therapy for adult Still's disease with marked thrombocytopenia

Clin Rheumatol. 1998;17(3):256-7. doi: 10.1007/BF01451061.

Abstract

A 34-year-old Japanese woman developed spiking fever, splenomegaly, arthritis, neutrophilia, hyperferritinaemia (22517 ng/ml), elevated C-reactive protein (9.1 mg/ml) and severe thrombocytopenia (1.7 x 10(4)/microl). The patient had depressed antithrombin III activity and abnormally high concentrations of both fibrin degradation products and thrombin-antithrombin complexes. This condition was resistant to high-dose prednisolone therapy (120 mg/day) and non-steroidal anti-inflammatory drugs. We initiated oral methotrexate therapy (7.5 mg/week, orally) with a favourable outcome. The patient's spiking fever subsided on the first day of methotrexate administration. Elevated levels of ferritin and C-reactive protein in the sera rapidly normalised. Methotrexate rapidly improved the disease state which suggested that methotrexate act via modulation of cytokine production or secretion.

Publication types

  • Case Reports

MeSH terms

  • Administration, Oral
  • Adult
  • Antimetabolites, Antineoplastic / therapeutic use*
  • Disease-Free Survival
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Methotrexate / therapeutic use*
  • Still's Disease, Adult-Onset / complications
  • Still's Disease, Adult-Onset / diagnosis
  • Still's Disease, Adult-Onset / drug therapy*
  • Thrombocytopenia / diagnosis
  • Thrombocytopenia / drug therapy*
  • Thrombocytopenia / etiology

Substances

  • Antimetabolites, Antineoplastic
  • Methotrexate