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Wegener's granulomatosis presenting as a pleural effusion

机译:韦格纳肉芽肿呈胸腔积液

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摘要

Wegener's granulomatosis is one of the pauci-immune small vessel vasculitides. It classically presents with the triad of upper and lower respiratory tract granulomas and necrotising focal segmental glomerulonephritis. It is associated with the presence in the serum of autoantibodies against components of neutrophil cytoplasm―antineutrophil cytoplasmic autoantibodies (ANCA). The illness can develop at any age but is more common in patients in their 50s and 60s and in men. The incidence of vasculitis is increasing, with about 10-20 people per million affected. We present a case that in retrospect had many clues at the initial time of admission, but it took five months and six different hospital teams to make the diagnosis.
机译:韦格纳肉芽肿病是免疫弱免疫的小血管之一。它典型地表现为上下呼吸道肉芽肿和坏死性节段性肾小球肾炎的三联征。它与血清中针对嗜中性粒细胞胞质成分的自身抗体-抗中性粒细胞胞质自身抗体(ANCA)的存在有关。该病可在任何年龄发展,但在50多岁和60多岁的患者以及男性中更为常见。血管炎的发病率正在增加,每百万人中约有10-20人受到影响。我们回顾了一个病例,该病例回顾了最初入院时的许多线索,但是花了五个月的时间和六个不同的医院团队才能做出诊断。

著录项

  • 来源
    《British Medical Journal》 |2003年第7406期|p.95-96|共2页
  • 作者

    Adrian G Blundell; Simon Roe;

  • 作者单位

    Nottingham Renal and Transplant Unit, Nottingham City Hospital, Nottingham NG5 1PB;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
  • 关键词

  • 入库时间 2022-08-18 00:12:20

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