Eosinophilia and hyperimmunoglobulinemia E as the presenting manifestations of Wegener's granulomatosis

Clin Rheumatol. 2003 Oct;22(4-5):333-5. doi: 10.1007/s10067-003-0725-2.

Abstract

Eosinophilia has long been known as a hallmark of Churg-Strauss syndrome but has rarely been reported in Wegener's granulomatosis (WG). Here we describe a patient with WG who had skin, kidney and lung involvement as well as striking peripheral eosinophilia and hyperimmunoglobulinaemia E (hyper-IgE). The patient's clinical picture was complicated by intra-alveolar haemorrhage resulting in severe anaemia and respiratory failure. The pulmonary symptoms recovered completely, but the renal involvement evolved into end-stage renal failure despite intensive immunosuppressive treatment, intravenous immunoglobulin and plasmapheresis. We suggest that the presence of eosinophilia and hyper-IgE might contribute to the development of different disease patterns in WG.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Blood Chemical Analysis
  • Cyclophosphamide / therapeutic use
  • Diagnosis, Differential
  • Drug Therapy, Combination
  • Female
  • Follow-Up Studies
  • Granulomatosis with Polyangiitis / diagnosis*
  • Granulomatosis with Polyangiitis / drug therapy
  • Humans
  • Immunoglobulin E / metabolism
  • Job Syndrome / diagnosis*
  • Methylprednisolone / administration & dosage
  • Pulmonary Eosinophilia / diagnosis*
  • Radiography, Thoracic
  • Risk Assessment
  • Severity of Illness Index
  • Tomography, X-Ray Computed
  • Treatment Outcome

Substances

  • Immunoglobulin E
  • Cyclophosphamide
  • Methylprednisolone