Complete haematological and cytogenetic response to interferon alpha-2a of a myeloproliferative disorder with eosinophilia associated with a unique t(4;7) aberration

Ann Hematol. 2000 Feb;79(2):95-8. doi: 10.1007/s002770050018.

Abstract

A female patient with eosinophilia and cardiac symptoms was found to have a unique chromosomal aberration [t(4;7)(q11;p13)] of bone-marrow precursors. The disorder was classified as a chronic myeloproliferative syndrome with eosinophilia. Due to a significant increase in the white blood cell and eosinophil count during initial treatment with prednisone and hydroxyurea, Interferon alpha-2a was administered at a dose of 3-5 x 10(6) I.U. s.c., five times per week, and induced a long-term complete haematological and cytogenetic response. The clinical features of this case are presented and discussed in the context of the current literature.

Publication types

  • Case Reports

MeSH terms

  • Bone Marrow Cells / pathology
  • Chromosomes, Human, Pair 4*
  • Chromosomes, Human, Pair 7*
  • Eosinophilia / complications*
  • Female
  • Humans
  • Hypereosinophilic Syndrome / genetics*
  • Interferon alpha-2
  • Interferon-alpha / genetics*
  • Interferon-alpha / therapeutic use*
  • Karyotyping
  • Myeloproliferative Disorders / complications*
  • Myeloproliferative Disorders / drug therapy*
  • Myeloproliferative Disorders / genetics
  • Recombinant Proteins
  • Translocation, Genetic*

Substances

  • Interferon alpha-2
  • Interferon-alpha
  • Recombinant Proteins