Bladder Cancer versus Hemorrhagic Cystitis: A Case of Mistaken Identity in a 34-Year-Old Male Undergoing Therapy for Granulomatosis with Polyangiitis.

Case reports in nephrology and urology Pub Date : 2014-06-04 eCollection Date: 2014-05-01 DOI:10.1159/000363692
Jonathan Amatruda, Kevin Dieckhaus, Poornima Hegde, John Taylor
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引用次数: 2

Abstract

A 34-year-old male was referred for management of bladder cancer noted on workup for gross hematuria and new-onset irritative voiding symptoms. The patient's history was significant for recently diagnosed granulomatosis with polyangiitis for which he was undergoing treatment with oral cyclophosphamide and corticosteroids. Cystoscopy revealed lesions suspicious for malignancy, but the patient was diagnosed with hemorrhagic cystitis secondary to BK virus infection upon cytology review, and immunostaining confirmed a polyomavirus infection of the urothelium. The patient's symptoms resolved after a modification of his immunosuppressive regimen, and antiviral therapy was ultimately unnecessary. Though symptomatic BK virus infection of the genitourinary tract is common in immunosuppressed transplant patients, its occurrence in a patient undergoing immunomodulation for an autoimmune disease has not been reported yet. This case illustrates the potential for active BK virus infections in atypical patient populations and underscores the importance of rigorous hematuria workup, particularly in patients with multiple risk factors.

Abstract Image

Abstract Image

膀胱癌与出血性膀胱炎:一例34岁男性肉芽肿合并多血管炎治疗的误诊。
一名34岁男性因膀胱癌接受检查,发现血尿和新发刺激性排尿症状。患者的历史是最近诊断肉芽肿病多血管炎,他正在接受口服环磷酰胺和皮质类固醇治疗。膀胱镜检查显示病变疑似恶性肿瘤,但细胞学检查诊断为继发于BK病毒感染的出血性膀胱炎,免疫染色证实尿路上皮多瘤病毒感染。患者的症状在免疫抑制方案的修改后消失,抗病毒治疗最终是不必要的。虽然有症状的BK病毒感染在免疫抑制移植患者中很常见,但在自身免疫性疾病的免疫调节患者中发生尚未见报道。该病例说明了在非典型患者人群中存在活动性BK病毒感染的可能性,并强调了严格血尿检查的重要性,特别是在具有多种危险因素的患者中。
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