Affiliations 

  • 1 Divisão de Reumatologia, Departamento de Medicina, Hospital Raja Permaisuri Bainun, Ipoh, Perak, Malásia
  • 2 Divisão de Reumatologia, Departamento de Medicina, Hospital Raja Permaisuri Bainun Ipoh, Perak, Malásia. Electronic address: ongps@hotmail.com
  • 3 Departamento de Patologia, Hospital Raja Permaisuri Bainun Ipoh, Perak, Malásia
Rev Bras Reumatol Engl Ed, 2014 Sep-Oct;54(5):393-6.
PMID: 25627304 DOI: 10.1016/j.rbr.2013.03.002

Abstract

Eosinophilic granulomatosis with polyangiitis is a rare primary vasculitic disease characterized by hypereosinophilia, late onset asthma and extravascular eosinophil granulomas. We report a case presented initially with acute myocardial infarction which later only proceed with asthma, skin manifestations and peripheral neuropathy. Laboratory parameters showed hypereosinohpilia with negative perinuclear pattern of antineutrophil cytoplasmic autoantibodies (p-ANCA). Skin biopsy showed leucocytoclastic vasculitis with eosinophilic infiltration while coronary angiography was normal. The patient's symptoms improved with IV methylprednisolone, pulse cyclophosphamide and azathioprine.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.