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

机译:模拟子宫宫颈腺癌的异位输尿管肿瘤:病例报告及简要回顾

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摘要

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.
机译: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发生在一名妇女的异位输尿管中,并模仿子宫宫颈腺癌。一名先前被诊断患有双角子宫的34岁女性,表现出性交后出血。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。骨盆超声和磁共振成像显示,异位肿瘤输尿管引流了骨盆增生异常,并插入了双角子宫的子宫颈。该患者接受了根治性子宫切除术和左肾切除术治疗。病理检查显示异位输尿管中出现腺癌。我们建议该病例可以作为建议对患有异位输尿管的女性进行定期随访以检测恶性转化的依据。

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