Borkum M, Abdelrahman H Y, Roberts R, Kalla A A, Okpechi I G
Division of Nephrology and Hypertension, Faculty of Health Sciences, University of Cape Town, South Africa.
S Afr Med J. 2016 Nov 2;106(11):1086-1087. doi: 10.7196/SAMJ.2016.v106i11.11083.
Polyarteritis nodosa (PAN) of the urinary tract is rare. An unusual case of systemic PAN involving the bladder neck is described. A 27-year-old man, with known diastolic hypertension diagnosed 2 years earlier, was admitted with chronic urinary obstruction complicated by hydronephrosis. He had symptoms of myalgia and weight loss, was afebrile but had an elevated erythrocyte sedimentation rate and acute-on-chronic renal impairment. All virological and serological tests including hepatitis B and anti-neutrophil cytoplasmic antibody were negative. A computed tomography scan of the brain revealed small-vessel disease. A bladder neck mass was visualised on cystoscopy. Histological examination of this demonstrated a medium-sized necrotising vasculitis with small-vessel fibrinoid necrosis suggestive of PAN. At least six of the American College of Rheumatology criteria for PAN were met. The patient was treated with pulses of intravenous cyclophosphamide and oral corticosteroids with a good clinical response.
泌尿道结节性多动脉炎(PAN)较为罕见。本文描述了一例累及膀胱颈的系统性PAN罕见病例。一名27岁男性,2年前被诊断为舒张期高血压,因慢性尿路梗阻并发肾积水入院。他有肌痛和体重减轻症状,无发热,但红细胞沉降率升高且存在慢性肾损伤急性加重。所有病毒学和血清学检查,包括乙肝和抗中性粒细胞胞浆抗体检查均为阴性。脑部计算机断层扫描显示有小血管疾病。膀胱镜检查可见膀胱颈肿物。对其进行组织学检查,结果显示为中等大小的坏死性血管炎,伴有小血管纤维蛋白样坏死,提示为PAN。该患者至少符合美国风湿病学会制定的PAN标准中的六项。患者接受了静脉注射环磷酰胺冲击治疗和口服糖皮质激素治疗,临床反应良好。