Prostatitis As An Initial Presentation For Granulomatosis With Polyangiitis.

Nauman Ismat Butt, Raheel Younus, Muhammad Qasim Khan Tareen, Sumaira Farman, Nighat Mir Ahmad, Amna Ahmad
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Abstract

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.

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前列腺炎是肉芽肿合并多血管炎的最初表现。
肉芽肿病合并多血管炎(GPA)是一种罕见的少免疫小血管坏死性肉芽肿性血管炎,多见于45-60岁。我们提出一个病例,以前健康的44岁男性表现为排尿困难和间歇性尿潴留8个月,没有响应经验抗生素治疗和TURP。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,但培养未见生长。随后他主诉发烧、咳嗽、呼吸困难和皮肤溃疡。胸部CT显示多发空化灶及胸腔积液。在工作中,c-ANCA阳性,诊断为肉芽肿病合并多血管炎。图示罕见的前列腺炎为GPA的初始特征。
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