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Congenital Mid Ureteric Valve Stenosis Revisited: Case Report and Review of the Literature

机译:先天性输尿管中段狭窄再诊:病例报告及文献复习

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摘要

Congenital mid ureteric valve (MUV) stenosis is a very rare entity. Definitive preoperative diagnosis is clinically challenging, and most patients are misdiagnosed preoperatively. Intraoperative identification is therefore very important. Curative treatment consists of excision of the involved ureteric segment and anastomosis. This report describes the clinical findings in a patient with congenital mid ureteric valve stenosis, including radiological and histological workup and operative management. Routine intraoperative retrograde pyelography is important in the diagnosis of such rare pathologies.
机译:先天性输尿管中段(MUV)狭窄是非常罕见的实体。明确的术前诊断在临床上具有挑战性,大多数患者术前被误诊。因此,术中识别非常重要。治愈性治疗包括切除受累输尿管段和吻合。该报告描述了先天性输尿管中段狭窄患者的临床发现,包括放射学和组织学检查以及手术管理。常规术中逆行肾盂造影对此类罕见病的诊断很重要。

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