A tumor of an ectopic ureter mimicking uterine cervix adenocarcinoma: case report and brief review.

Mehdi Jaidane, Adel Slama, Mohammed Bibi
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引用次数: 6

Abstract

Single system ectopic ureter is a rare congenital malformation of the urinary tract, frequently associated with genital tract malformations. We report the first case of an adenocarcinoma arising in an ectopic ureter in a woman and mimicking uterine cervical adenocarcinoma. A 34-year-old woman, previously diagnosed as having bicornuate uterus, presented with post-coital bleeding. On gynecological exam, there were two cervixes with a small nodule on the left cervix. After nodule biopsy, the initial diagnosis was adenocarcinoma of the uterine cervix. Pelvic ultrasound and magnetic resonance imaging demonstrated an ectopic tumoral ureter draining a dysplastic pelvic kidney and inserted in the cervix of a bicornuate uterus. The patient was treated by radical hysterectomy and left nephroureterectomy. Pathological exam demonstrated an adenocarcinoma arising in the ectopic ureter. We suggest that this case could be an argument for recommending regular follow-up for women with ectopic ureter for detecting malignant transformation.

异位输尿管肿瘤模拟子宫颈腺癌1例报告及简要回顾。
单系统异位输尿管是一种罕见的先天性泌尿道畸形,通常与生殖道畸形有关。我们报告的第一例腺癌出现在异位输尿管在一个女人和模仿子宫颈腺癌。34岁女性,先前诊断为双角子宫,表现为性交后出血。在妇科检查中,有两个子宫颈,左侧子宫颈有一个小结节。结节活检后,初步诊断为子宫颈腺癌。盆腔超声和磁共振成像显示一个异位肿瘤输尿管引流发育不良的盆腔肾并插入双角子宫子宫颈。患者行根治性子宫切除术和左肾输尿管切除术。病理检查显示异位输尿管发生腺癌。我们认为这个病例可以作为建议对异位输尿管妇女定期随访以检测恶性转化的论据。
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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