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Rare disease: Rituximab seems a promising therapeutic option in granulomatosis with polyangiitis with intestinal perforation: a case report and literature review

机译:罕见疾病:利妥昔单抗似乎在肉芽肿合并多血管炎伴肠穿孔的治疗中是一种有前途的治疗选择:一例病例并文献复习

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摘要

Granulomatosis with polyangiitis (Wegener's) (GPA) is a chronic disease of unknown aetiology that leads to necrotising vasculitis in small and medium-sized vessels characterised by respiratory system and kidney involvement. Intestinal involvement is rare and perforation is even rarer in GPA. In this study, we are presenting a literature review of related cases, and a 29-year-old man referred from the emergency department with a multiple distal ileal perforation that was diagnosed with GPA, and successfully treated with rituximab.
机译:肉芽肿性多血管炎(Wegener's)(GPA)是一种病因不明的慢性疾病,导致中小血管坏死性血管炎,其特征是呼吸系统和肾脏受累。肠道受累很少见,GPA穿孔很少见。在这项研究中,我们将提供相关病例的文献综述,并从急诊科转诊的一名29岁男子患有多发性回肠远端穿孔,被诊断为GPA,并成功用利妥昔单抗治疗。

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