Butt Nauman Ismat, Younus Raheel, Khan Tareen Muhammad Qasim, Farman Sumaira, Ahmad Nighat Mir, Ahmad Amna
Department of Medicine & Allied, Azra Naheed Medial College Superior University Lahore.
Department of Rheumatology, National hospital and Medical Center Lahore.
J Ayub Med Coll Abbottabad. 2022 Oct-Dec;34(Suppl 1)(4):S1043-S1045. doi: 10.55519/JAMC-04-S4-10658.
Granulomatosis with polyangiitis (GPA) is an uncommon pauci-immune small-vessel necrotising granulomatous vasculitis mostly seen in age 45-60 years. We present the case of a formerly healthy 44 years old male presenting with dysuria and intermittent urinary retention for 8 months, not responding to empirical antibiotic therapy and TURP. A prostate biopsy showed necrotising granulomatous prostatitis. Urinalysis demonstrated persistent pyuria and haematuria, but cultures showed no growth. Subsequently he complained of fever, cough, dyspnoea and skin ulcers. CT of the chest showed multiple cavitatory lesions and pleural effusion. On work up, c-ANCA was positive and a diagnosis of granulomatosis with polyangiitis was established. This depicts a rarely seen presentation of prostatitis as the initial feature of GPA.
肉芽肿性多血管炎(GPA)是一种罕见的少免疫性小血管坏死性肉芽肿性血管炎,多见于45至60岁人群。我们报告一例病例,一名44岁既往健康男性,出现尿痛和间歇性尿潴留8个月,经验性抗生素治疗和经尿道前列腺电切术均无效。前列腺活检显示坏死性肉芽肿性前列腺炎。尿液分析显示持续脓尿和血尿,但培养无细菌生长。随后,他出现发热、咳嗽、呼吸困难和皮肤溃疡。胸部CT显示多个空洞性病变和胸腔积液。经检查,c-ANCA阳性,确诊为肉芽肿性多血管炎。这描述了一种罕见的表现,即前列腺炎作为GPA的初始特征。