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Giant hydronephrosis secondary to ureteropelvic junction obstruction a rare occurrence case report

机译:巨肾性肾小粒继承给输尿管尿道接线梗阻罕见发生案例报告

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摘要

Giant hydronephrosis (GH) is very rare in adults. We report a case of a 46-year-old man who presented with progressively increasing abdominal swelling. A contrast-enhanced CT scan of the abdomen and pelvis was used for the diagnosis. Left side open nephrectomy was performed and 22 L fluid was evacuated. UPJ obstruction was noted intraoperatively. No recurrence of abdominal swelling was noted on follow up examination.
机译:巨水分(GH)在成年人中非常罕见。我们举报了一个46岁男子的案例,他们呈逐渐增加腹部肿胀。腹部和骨盆的对比增强CT扫描用于诊断。进行左侧开孔肾切除术,并抽空22L液体。 UPJ障碍被术中注意到。在后续检查中未注意到腹部肿胀的复发。

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