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隐匿却具侵袭性:一名29岁男性膀胱肉瘤样癌病例报告,表现为膀胱皮肤瘘且无血尿

Silent but Invasive: A Case Report of a Sarcomatoid Bladder Carcinoma in a 29-Year-Old Male Presenting As Vesico-Cutaneous Fistula Without Hematuria.

作者信息

Agarwal Neeraj, Kumawat Rajesh K, Sharma Sarthak, Gupta Prashant, Jangid Dharmendra K

机构信息

Urology and Renal Transplant Surgery, Sawai Man Singh Medical College, Jaipur, IND.

出版信息

Cureus. 2025 Jul 18;17(7):e88261. doi: 10.7759/cureus.88261. eCollection 2025 Jul.

Abstract

Sarcomatoid urothelial carcinoma (SUC) is a rare and aggressive variant of urinary bladder cancer and is associated with a poor prognosis. This case report presents the unusual case of a 29-year-old male who presented with a vesicocutaneous fistula causing continuous suprapubic urine leakage for four months following a previous bladder surgery for a vesical calculus. This patient had no history of hematuria, which is a common symptom of bladder cancer. Investigations, including contrast-enhanced computed tomography (CECT) and 18F-fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET-CT), revealed a large, locally advanced bladder mass infiltrating the anterior abdominal wall with a vesicocutaneous fistula. The patient underwent a radical cystoprostatectomy, wide local excision of the fistulous tract, bilateral pelvic lymph node dissection, right cutaneous ureterostomy, and abdominal wall reconstruction with a pedicled anterolateral thigh flap. Histopathology confirmed poorly differentiated SUC. This case is unique due to the patient's young age, the atypical presentation with a vesicocutaneous fistula without hematuria, and the sarcomatoid histology. It highlights the aggressive nature of SUC, its potential for unusual presentations that can delay diagnosis, and the necessity of considering bladder cancer in young patients with urinary fistulas, even without hematuria. Radical surgery with meticulous reconstruction offers the best chance for disease control in such complex scenarios, emphasizing the importance of early suspicion and multidisciplinary management.

摘要

肉瘤样尿路上皮癌(SUC)是膀胱癌一种罕见且侵袭性强的变异类型,预后较差。本病例报告呈现了一名29岁男性的不寻常病例,该患者在先前因膀胱结石进行膀胱手术后出现膀胱皮肤瘘,导致耻骨上持续漏尿四个月。该患者无血尿病史,而血尿是膀胱癌的常见症状。包括增强计算机断层扫描(CECT)和18F-氟脱氧葡萄糖(FDG)正电子发射断层扫描-计算机断层扫描(PET-CT)在内的检查显示,有一个巨大的、局部进展性膀胱肿块,侵犯前腹壁并伴有膀胱皮肤瘘。患者接受了根治性膀胱前列腺切除术、瘘管广泛局部切除术、双侧盆腔淋巴结清扫术、右侧皮肤输尿管造口术以及带蒂股前外侧皮瓣腹壁重建术。组织病理学证实为低分化SUC。该病例独特之处在于患者年轻、无血尿的膀胱皮肤瘘非典型表现以及肉瘤样组织学特征。它突出了SUC的侵袭性本质、其可能出现延迟诊断的不寻常表现,以及在即使无血尿的年轻尿瘘患者中考虑膀胱癌的必要性。在这种复杂情况下,精心重建的根治性手术为疾病控制提供了最佳机会,强调了早期怀疑和多学科管理的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e783/12358243/045ac6729a6c/cureus-0017-00000088261-i01.jpg

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