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抗中性粒细胞胞浆自身抗体相关性血管炎的诊断分类

Diagnostic classification of antineutrophil cytoplasmic autoantibody-associated vasculitides.

作者信息

Jennette J C, Falk R J

机构信息

Department of Pathology, School of Medicine, University of North Carolina, Chapel Hill 27599.

出版信息

Am J Kidney Dis. 1991 Aug;18(2):184-7. doi: 10.1016/s0272-6386(12)80878-x.

Abstract

Antineutrophil cytoplasmic autoantibodies (ANCA) are in the circulation of patients with a variety of clinically and pathologically distinctive forms of necrotizing vasculitis. Some patients have classic manifestations of well-recognized clinicopathologic syndromes, such as Wegener's granulomatosis, microscopic polyarteritis nodosa, and Churg-Strauss syndrome, but many patients are difficult to assign to a diagnostic category. The Ad Hoc Nomenclature Committee of The Third International Workshop on ANCA is attempting to identify a working classification system for ANCA-associated vasculitides. This system takes into account the many shared clinical and pathologic features, and relies on prerequisite positive and negative findings for diagnostic categorization.

摘要

抗中性粒细胞胞浆自身抗体(ANCA)存在于患有各种临床和病理特征各异的坏死性血管炎患者的血液循环中。一些患者具有公认的临床病理综合征的典型表现,如韦格纳肉芽肿、显微镜下多动脉炎结节和变应性肉芽肿性血管炎,但许多患者难以归入某一诊断类别。第三届国际ANCA研讨会特设命名委员会正在尝试确定一种用于ANCA相关性血管炎的实用分类系统。该系统考虑到许多共同的临床和病理特征,并依靠诊断分类所需的阳性和阴性结果。

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