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Congenital ureteral valves: report of 2 cases

机译:先天性输尿管瓣膜:2例报告

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摘要

Congenital ureteral valves have not been a well recognized condition for the cause of ureteral obstruction. In our first case a 21-year-old male presented with left flank pain. Intravenous urography showed left mild hydronephrosis due to upper ureteral obstruction. Partial ureteral resection and re-anastomosis was performed. Histology demonstrated mucosal folds with smooth muscle. In our second case a 12-year-old boy presented with left flank pain. Retrograde pyelogram showed a fold-like filing defect which suggested ureteral valve. Endoscopical valve resection through nephrostomy was performed. Optimal management and diagnostic difficulties were discussed.
机译:对于输尿管阻塞的原因,先天性输尿管瓣膜尚未得到公认。在我们的第一个案例中,一名21岁的男性表现出左胁腹疼痛。静脉输尿管造影显示由于上输尿管阻塞而导致左轻度肾盂积水。进行部分输尿管切除和再吻合术。组织学显示粘膜褶皱与平滑肌。在我们的第二例中,一个12岁的男孩表现出左胁疼痛。逆行肾盂造影显示出折叠状锉屑缺损,提示输尿管瓣膜。通过肾造口术进行内窥镜瓣膜切除术。讨论了最佳管理和诊断困难。

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