Anderson Patrick T, Gottheil Stephanie, Gabril Manal, Barra Lillian, Power Nicholas
Department of Surgery, Division of Urology, University of Ottawa, The Ottawa Hospital, Ottawa, ON, Canada.
Department of Medicine, Division of Rheumatology; Schulich School of Medicine and Dentistry, Western University, London Health Sciences Centre, London, ON, Canada.
Can Urol Assoc J. 2017 Jan-Feb;11(1-2):E38-E40. doi: 10.5489/cuaj.3555. Epub 2017 Jan 12.
Granulomatosis with polyangiitis (GPA, formerly Wegener's granulomatosis) is a systemic necrotizing vasculitis of small- and medium-sized blood vessels, primarily affecting the upper and lower respiratory tracts, as well as the kidneys. Urogenital manifestations of GPA are exceedingly rare and usually respond well to systemic immunosuppressive therapy. Here, we present a case of a 36-year-old female presenting with acute urinary obstruction secondary to urethral GPA involvement in the immediate postpartum period. Special consideration should be given to ruling out malignancy in all patients with a history of GPA and urethral lesions, especially when there is a history of cyclophosphamide treatment.
肉芽肿性多血管炎(GPA,原韦格纳肉芽肿)是一种主要累及上、下呼吸道以及肾脏的中小血管系统性坏死性血管炎。GPA的泌尿生殖系统表现极为罕见,通常对全身免疫抑制治疗反应良好。在此,我们报告一例36岁女性病例,该患者在产后即刻因尿道GPA受累出现急性尿路梗阻。对于所有有GPA病史和尿道病变的患者,尤其是有环磷酰胺治疗史的患者,应特别考虑排除恶性肿瘤。