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Double trouble: diagnostic dilemma in a rare association of proximal ureteric valve with orthotopic ureterocele-case report

机译:双重麻烦:诊断困境,近端输尿管瓣膜具有原位尿辨座的近端输尿管阀的报告

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Background:Association of the ureterocele and proximal ureteral valve is a rare congenital anomaly which can lead to quick detoriation of renal function due to double obstruction. Though ureteral valves have been associated with other ureteral anomalies, this specific association is extremely rare.Case presentationA 7-month-old boy was referred to us for antenatally detected hydronephrosis. Provisional diagnosis of orthotopic ureterocele with pelviureteric junction (PUJ) obstruction was made based on preoperative imaging. Endoscopic incision of ureterocele was done and retrograde pyelography showed tight obstruction at PUJ which necessitated a pyeloplasty. Examination of resected specimen confirmed a ureteral valve. Postoperatively, the patient had good improvement in kidney function.ConclusionTo conclude, congenital ureteral valves are a rare cause of ureteric obstruction and its association with ureterocele is rarer still. Identification of an ureterocele should not deter us from searching for an associated pathology like a ureteric valve when imaging shows more severe hydronephrosis suggestive of more proximal obstruction.
机译:背景:尿素椰菜和近摄输尿管瓣的关联是一种罕见的先天性异常,可以导致由于双阻塞而快速地破坏肾功能。虽然输尿管阀与其他输尿管异常有关,但这种特定的关联是极为罕见的.CASE呈现,7个月大的男孩被提及给我们出现的肾内肾复子。基于术前成像,对盆腔插入(PUJ)阻塞的原位尿辨芯片梗死的临时诊断。尿素椰菜的内镜切口已完成,并逆行肾盂造影显示Puj的紧张梗阻,这需要脓细胞育术。切除试样的检查证实了输尿管阀。术后,患者对肾功能良好的改善。结论,先天性输尿管阀是输尿管梗阻的罕见原因,其与尿频丝的关联仍然是罕见的。当成像显示出更严重的肾盂血症时,不应该阻止我们在寻找带输尿管阀的相关病理学中寻找相关的病理学,这表明更严重的肾值眼呈现出更多的近端梗阻。

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