以腹部受累为主要表现的全身性或孤立性胃肠道血管炎

Gatr-alnada Gheriani, Petar S. Lenert
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引用次数: 0

摘要

全身性血管炎可引起各种胃肠道表现(GI),从轻微的、经常是非特异性的腹痛到可能危及生命的肠穿孔。全身性血管炎的血管受累可影响任何消化道血管,最常见的是肠系膜动脉、肝动脉或脾动脉。影响动脉血管壁不同层次的炎症变化可导致动脉瘤扩张或血管闭塞,随后器官缺血导致粘膜溃疡、消化道出血、穿孔或肠梗阻。虽然肠道外表现的出现可能有助于诊断,但延误适当的诊断和快速启动糖皮质激素和免疫抑制治疗可能会造成有害后果。对孤立性胃肠道血管炎的认识尤为重要,因为这种疾病在终末期器官损害明显之前往往得不到诊断。对于疑似消化道血管炎的患者,血管炎模拟物(如血管性埃勒斯-丹洛斯综合征或纤维肌发育不良)又增加了复杂性,因此应始终慎重考虑。
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Abdominal involvement as a primary manifestation of systemic or isolated gastrointestinal vasculitis
Systemic vasculitides can cause a wide variety of gastrointestinal manifestations (GI) ranging from mild and frequently nonspecific abdominal pains to potentially life-threatening bowel perforations. Vascular involvement in systemic vasculitides can affect any GI blood vessel, most commonly mesenteric, hepatic, or splenic arteries. Inflammatory changes affecting different layers of arterial vessel walls can lead to aneurysmatic dilatation or blood vessel occlusion with subsequent organ ischemia leading to mucosal ulcerations, GI bleeding, perforations, or bowel obstruction. While the presence of extraintestinal manifestations may aid in diagnosis, delays in making appropriate diagnoses and rapid initiation of glucocorticoid and immunosuppressive treatment can have detrimental consequences. Awareness of isolated gastrointestinal vasculitis is of particular importance as it frequently remains undiagnosed until end-stage organ damage becomes apparent. Vasculitis mimics such as vascular Ehlers-Danlos syndrome or fibromuscular dysplasia add another lay of complexity in approaching patients with suspected GI vasculitis and should always be carefully considered.
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