Tanaka Shinichi, Ohmine Takahiro, Maeda Takashi
Department of Surgery, Hiroshima Red Cross Hospital and Atomic-bomb Survivors Hospital, Hiroshima, Hiroshima, Japan.
Ann Vasc Dis. 2023;16(4):269-272. doi: 10.3400/avd.avd.cr.23-00050. Epub 2023 Oct 13.
An asymptomatic dissecting superior mesenteric artery (SMA) aneurysm in granulomatosis with polyangiitis (GPA), historically termed Wegener's granulomatosis, is rare. We herein describe a 68-year-old man who was diagnosed with GPA based on a high level of proteinase 3 (PR3)-antineutrophil cytoplasmic antibody (ANCA). One year after remission of GPA, the patient developed pyelonephritis, and his PR3-ANCA level increased again. Computed tomography showed a rapid increase in the size of the dissecting SMA aneurysm. The patient underwent successful endovascular stent-graft repair. At the time of this writing, 3 years had passed since the surgery and the clinical course was good.
在肉芽肿性多血管炎(GPA,既往称为韦格纳肉芽肿)中,无症状的肠系膜上动脉(SMA)夹层动脉瘤较为罕见。我们在此描述一名68岁男性,其基于高水平的蛋白酶3(PR3)-抗中性粒细胞胞浆抗体(ANCA)被诊断为GPA。GPA缓解一年后,患者发生肾盂肾炎,其PR3-ANCA水平再次升高。计算机断层扫描显示夹层SMA动脉瘤大小迅速增加。患者接受了成功的血管内支架植入修复术。在撰写本文时,手术已过去3年,临床过程良好。