Gastrointestinal aspects of vasculitides

被引:25
作者
Soowamber, Medha [1 ]
Weizman, Adam V. [2 ]
Pagnoux, Christian [1 ]
机构
[1] Univ Toronto, Mt Sinai Hosp, Div Rheumatol, Vasculitis Clin, 60 Murray St, Toronto, ON M5T 3L9, Canada
[2] Univ Toronto, Mt Sinai Hosp, Div Gastroenterol, Univ Hlth Network, 437-600 Univ Ave, Toronto, ON M5G 1X5, Canada
关键词
GIANT-CELL ARTERITIS; CHURG-STRAUSS-SYNDROME; HENOCH-SCHONLEIN PURPURA; SYSTEMIC-LUPUS-ERYTHEMATOSUS; INTESTINAL BEHCETS-DISEASE; OBLITERANS BUERGERS-DISEASE; ANCA-ASSOCIATED VASCULITIS; POOR-PROGNOSIS FACTORS; OF-THE-LITERATURE; TERM-FOLLOW-UP;
D O I
10.1038/nrgastro.2016.179
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Systemic vasculitides are caused by inflammation of blood vessels and can affect any organ and any part of the gastrointestinal tract, hepatic and biliary system, as well as the pancreas. These disorders can cause a wide array of gastrointestinal manifestations, from asymptomatic elevated transaminase levels and mild abdominal pain to potentially life-threatening bowel perforations and peritonitis. A diagnosis based solely on gastrointestinal symptoms is challenging as these manifestations are not specific. Conversely, diagnostic and therapeutic delays can be rapidly detrimental. In this article, we review the epidemiology, characteristics and management of the main gastrointestinal manifestations of systemic vasculitides, including polyarteritis nodosa and antineutrophil cytoplasm antibody-associated vasculitides, as well as isolated vasculitides limited to the gastrointestinal tract.
引用
收藏
页码:185 / 194
页数:10
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