Primary bulbar urethral adenocarcinoma arising from intestinal-type villous adenoma: a rare malignant entity

IF 0.5 Q4 UROLOGY & NEPHROLOGY
Urology Case Reports Pub Date : 2026-07-01 Epub Date: 2026-06-23 DOI:10.1016/j.eucr.2026.103519
Rachel Cockburn, Jennifer Xu, Hans Goossen
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引用次数: 0

Abstract

Primary urethral adenocarcinoma is rare, with limited guidance for management. A 65-year-old male presented with haematuria and urinary retention, found to have a bulbar urethral tumour at the site of previous stricture. Histology demonstrated moderately differentiated adenocarcinoma arising from an intestinal-type villous adenoma with high-grade dysplasia. Staging excluded metastatic or alternative primary disease. He underwent subtotal urethrectomy with perineal urethrostomy, achieving clear margins. Mild postoperative stenosis was managed conservatively. At one year, there is no recurrence. This case describes gastrointestinal adenocarcinoma in the setting of urethral stricture disease and highlights tailored surgical management in achieving favourable oncological and functional outcomes.
原发性球尿道腺癌起源于肠型绒毛腺瘤:一种罕见的恶性肿瘤。
原发性尿道腺癌是罕见的,治疗指导有限。65岁男性,因血尿和尿潴留,在先前狭窄部位发现球尿道肿瘤。组织学表现为中度分化腺癌,起源于肠型绒毛腺瘤伴高级别不典型增生。分期排除转移性或替代性原发疾病。他接受了次全尿道切除术和会阴尿道造口术,获得了清晰的边缘。术后轻度狭窄保守处理。一年后,没有复发。本病例描述了胃肠道腺癌在尿道狭窄疾病的背景下,并强调了量身定制的手术管理,以获得良好的肿瘤和功能结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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