Tak Gopal Ramdas, Agrawal Shashank, Desai Mahesh Ramanlal, Ganpule Arvind Prakash, Singh Abhishek Gajendra, Sabnis Ravindra Bhalchandra
Department of Urology, Muljibhai Patel Urological Hospital, Nadiad, India.
J Endourol Case Rep. 2020 Sep 17;6(3):128-131. doi: 10.1089/cren.2019.0148. eCollection 2020.
Ureteral hemangioma is a rare entity and few cases have been reported in the literature. Nearly all cases are diagnosed on pathologic examination postoperatively. In this study we report a 22 years young male patient presented with left-sided flank pain and hematuria. He underwent computed tomography, cystoscopy, left retrograde pyelogram, left side ureteroscopy, and urine cytology. Ureteroscopy showed a left upper ureteral narrowing with bulging mass above it. Robot-assisted segmental ureterectomy with end-to-end anastomosis over 6/26 Double-J stent was done and histopathologic examination of excised ureter reported ureteral hemangioma.
输尿管血管瘤是一种罕见的疾病,文献中报道的病例很少。几乎所有病例都是在术后病理检查时确诊的。在本研究中,我们报告了一名22岁的年轻男性患者,他出现左侧胁腹疼痛和血尿。他接受了计算机断层扫描、膀胱镜检查、左侧逆行肾盂造影、左侧输尿管镜检查和尿液细胞学检查。输尿管镜检查显示左输尿管上段狭窄,其上方有一个隆起的肿块。在6/26双J支架上进行了机器人辅助的节段性输尿管切除术并端端吻合,对切除的输尿管进行组织病理学检查报告为输尿管血管瘤。