Hypereosinophilic syndrome: case presentation and update

J Allergy Clin Immunol. 2004 Jan;113(1):50-8. doi: 10.1016/j.jaci.2003.10.051.

Abstract

Persistent peripheral blood eosinophilia can be associated with a variety of diseases, ranging from parasitic infection to gastrointestinal disease to vasculitis to the hypereosinophilic syndrome (HES). Mucosal ulcerations are a variant presentation of the HES that appear to be markers for a mutation that characterizes a subgroup of patients with HES responsive to treatment with imatinib mesylate. We present a patient with peripheral blood eosinophilia and severe recurrent mucosal ulcers and discuss his presentation in the context of new information about the evaluation, disease progression, and treatment of HES.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Blood Proteins
  • Diagnosis, Differential
  • Endocardium / pathology
  • Eosinophil Granule Proteins
  • Eosinophils / immunology*
  • Fatal Outcome
  • Heart Diseases / diagnosis
  • Humans
  • Hypereosinophilic Syndrome / diagnosis*
  • Hypereosinophilic Syndrome / therapy
  • Immunosuppressive Agents / therapeutic use
  • Interferon-alpha / therapeutic use
  • Leukocyte Count
  • Male
  • Oral Ulcer / diagnosis*
  • Oral Ulcer / therapy
  • Penile Diseases / diagnosis*
  • Penile Diseases / therapy
  • Ribonucleases / blood
  • Skin Ulcer / diagnosis
  • Splenectomy

Substances

  • Blood Proteins
  • Eosinophil Granule Proteins
  • Immunosuppressive Agents
  • Interferon-alpha
  • Ribonucleases