作者: Loïc Guillevin , Bernard Jarrousse
DOI: 10.1007/978-3-642-58314-8_24
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摘要: Antineutrophil cytoplasmic antibodies (ANCA) are the immunological hallmark of several systemic vasculitides. Since description ANCA-associated vasculitides[ 1], ANCA have been demonstrated to be associated with small-sized vasculitides, such as Wegener’s granulomatosis (WG) [2], Churg-Strauss syndrome (CSS) [3, 4, 5] and microscopic polyangiitis (MPA)[6]. Although considered useful for diagnosis their significance follow-up remains controversial probably differs from one vasculitis another.