首页> 美国卫生研究院文献>Journal of Clinical and Diagnostic Research : JCDR >Bilateral Single System Orthotopic Ureterocele with Bilateral Multiple Calculi Presented with Retention of Urine - an Urological Emergency
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Bilateral Single System Orthotopic Ureterocele with Bilateral Multiple Calculi Presented with Retention of Urine - an Urological Emergency

机译:单侧双系统原位输尿管上皮囊肿伴双侧多结石伴尿Re留-泌尿外科急诊

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摘要

The ureterocele is an uncommon congenital anomaly of the lower ureter. Ureterocele with a single pelvicalyceal system, bilateral, and orthotopic variety is less common. Calculi within bilateral ureterocele are a rare occurrence. To the best of our knowledge, only a few similar cases have been reported in the literature. Among the all reported presentations of this type of ureterocele, presentation with Acute Urinary Retention (AUR) has not been described in the literature. We present a case of nine-year-old child having bilateral, single system orthotopic ureterocele with calculi in bilateral ureterocele and presented with AUR due to obstructive bulbar urethral calculus. The bilateral endoscopic incision was given and all four calculi were removed endoscopically through percutaneous route. Voiding cystourethrography after two years follow-up was non-refluxing. The purpose of reporting this case is the rarity of the disease and to emphasize that delay in diagnosis and treatment of these cases may lead to complications such as recurrent urinary tract infection and renal failure.
机译:输尿管膨出是下输尿管的一种罕见的先天性异常。具有单个骨盆腔系统,双侧和原位变体的输尿管静脉膨出较少见。输尿管双侧结石很少发生。据我们所知,文献中仅报道了少数类似病例。在所有报道的这种输尿管囊肿的表现中,急性尿tention留(AUR)表现都没有在文献中描述。我们介绍了一个9岁儿童,其双侧输尿管膨出有双侧单系统原位输尿管膨出并结石,并因梗阻性延髓性尿道结石而出现了AUR。给予双侧内窥镜切口,并通过经皮内窥镜切除所有四个结石。两年的随访后行膀胱尿道造影是无反流的。报告该病例的目的是该病的罕见性,并强调延迟诊断和治疗这些病例可能导致并发症,例如尿路反复感染和肾功能衰竭。

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