原发性输尿管粘液腺癌伴黄色肉芽肿性肾盂肾炎,伪装成巨大的肾脏肿块

A. Kanbur, Atul Mokashi, S. Dutta, A. Hase
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摘要

原发性输尿管癌在所有泌尿生殖系统恶性肿瘤中是罕见的,移行细胞癌是最常见的组织学,其次是鳞状细胞癌。腺癌极为罕见。在此,我们报告一例67岁男性右输尿管下段原发性粘液分泌腺癌。增强计算机断层扫描(CECT)显示一个巨大的囊性肿块占据整个腹部,并在右输尿管下三分之一处有一个肿块,酷似巨大的肾肿块。输尿管镜检查后进行剖腹手术,包括右肾输尿管切除术和膀胱袖切除术。组织病理学检查,基于CECT扫描的疑似巨大肾脏肿块显示为肾脏黄色肉芽肿性肾盂肾炎并输尿管原发性粘液分泌腺癌。
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Primary ureteral mucinous adenocarcinoma with xanthogranulomatous pyelonephritis masquerading as a giant renal mass
Primary ureteral carcinoma is rare among all urogenital malignancies, with transitional cell carcinoma being the most common histology followed by squamous cell carcinoma. Adenocarcinoma is extremely rare. Herein, we report a case of primary mucin secreting adenocarcinoma of the right lower ureter in a 67-year-old male. Contrast-enhanced computed tomography (CECT) scan showed a large cystic mass occupying the whole abdomen along with a mass in the lower third of the right ureter mimicking as a giant renal mass. Ureteroscopy followed by laparotomy including right nephroureterectomy with bladder cuff excision was performed. On histopathological examination, the CECT scan-based suspected giant renal mass revealed to be xanthogranulomatous pyelonephritis of the kidney along with primary mucin secreting adenocarcinoma of the ureter.
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