Manifestations mimicking relapsing polychondritis in a patient with microscopic polyangiitis

Hiroe Ogawa, Eiko Nishi, Hideto Kameda, Koichi Amano, Tsutomu Takeuchi

研究成果: Article査読

1 被引用数 (Scopus)

抄録

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.

本文言語English
ページ(範囲)104-108
ページ数5
ジャーナルJapanese Journal of Clinical Immunology
28
2
DOI
出版ステータスPublished - 2005
外部発表はい

ASJC Scopus subject areas

  • 免疫アレルギー学
  • 免疫学

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