Rolak Stacey, Pham Michael M, Lam-Himlin Dora M, Batheja Mashal J
Division of Gastroenterology and Hepatology, Mayo Clinic-Arizona, Phoenix, AZ.
Division of Rheumatology, Mayo Clinic-Arizona, Phoenix, AZ.
ACG Case Rep J. 2025 Jun 25;12(6):e01746. doi: 10.14309/crj.0000000000001746. eCollection 2025 Jun.
Granulomatosis with polyangiitis (GPA) is a rare small vessel vasculitis that commonly presents with multiorgan involvement of the upper airways, lungs, and kidneys. We report a 55 year-old-man who presented with painful oral ulcers, diffuse joint pain, epistaxis, and intermittent maroon bowel movements. Infectious evaluation was unremarkable. Rheumatologic evaluation demonstrated elevated c-anti-neutrophil cytoplasmic antibody and proteinase 3 antibodies. Colonoscopy with terminal ileum biopsies demonstrated angiocentric inflammatory findings supportive of a diagnosis of GPA. This case was unusual in its presentation with predominately oral manifestations. A diagnosis of GPA should remain on the differential for patients with gastrointestinal bleeding, and these systemic symptoms require a high level of suspicion to lead to timely diagnosis.
肉芽肿性多血管炎(GPA)是一种罕见的小血管血管炎,通常表现为上呼吸道、肺和肾脏的多器官受累。我们报告一名55岁男性,他出现疼痛性口腔溃疡、弥漫性关节疼痛、鼻出血和间歇性暗红色排便。感染性评估无异常。风湿学评估显示抗中性粒细胞胞浆抗体和蛋白酶3抗体升高。结肠镜检查及回肠末端活检显示血管中心性炎症表现,支持GPA的诊断。该病例的表现以口腔症状为主,较为罕见。对于有胃肠道出血的患者,应将GPA诊断纳入鉴别诊断范围,这些全身症状需要高度怀疑才能及时诊断。