Japanese Journal of Clinical Immunology
Online ISSN : 1349-7413
Print ISSN : 0911-4300
ISSN-L : 0911-4300
Case Reports
Manifestations mimicking relapsing polychondritis in a patient with microscopic polyangiitis.
Hiroe OGAWAEiko NISHIHideto KAMEDAKoichi AMANOTsutomu TAKEUCHI
Author information
JOURNAL FREE ACCESS

2005 Volume 28 Issue 2 Pages 104-108

Details
Abstract
  Microscopic polyangiitis (MPA) is a systemic disorder characterized by inflammation of small vessels mainly affecting the kidneys and lungs.
  We describe a 72-year-old woman who developed multiple cartilage involvements as well as major manifestations of MPA. The left ear biopsy demonstrated cartilaginous inflammation and small vessel vasculitis. She also had conjunctivitis, hearing impairment, interstitial lung disease, glomerulonephritis with vasculitis and mononeuritis multiplex. Serological examinations revealed a positive antineutrophil cytoplasmic antibody (PR-3 ANCA). Cyclophosphamide and oral corticosteroid therapy was instituted and remission achieved. Due to lacks of nasal and bronchial involvements, as well as the evidence of auricular vasculitis, we concluded that her findings mimicking relapsing polychondritis developed as systemic manifestations of MPA.
Content from these authors
© 2005 The Japan Society for Clinical Immunology
Previous article
feedback
Top