结石引起的右侧两个独立骨盆系统伴双输尿管的肾盂肾盂积水梗阻性综合征:罕见的临床病例。

A. Gautam, Bijay Subedi, M. Dhital, J. Awasthi, S. Adhikari, Purushottam Adhikari
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引用次数: 0

摘要

摘要输尿管积水是一种因梗阻导致肾盂和输尿管同时扩张的临床疾病。当两个输尿管来自单个肾脏时,称为输尿管双裂,可能是完整的,也可能是不完整的。本文报告一名38岁成年男性,先天性输尿管双裂异常及结石引起的梗阻性输尿管积水的罕见临床表现。这种情况的常见症状是腹部极度难以忍受的疼痛,腰部至腹股沟的中度至重度疼痛,呕吐/恶心和血尿。诊断是通过静脉注射染料和计算机断层扫描静脉肾盂造影和实验室结果。在这个病例中,我们发现了两个不完全输尿管,即起源于右肾的双裂性输尿管在排空进入膀胱之前合并为一个输尿管。在L3椎体水平双输尿管交界处出现单个大结石,大小约为8.6*8mm,引起输尿管积水。右上输尿管上游同样明显扩张。输尿管双裂畸形是由于输尿管憩室分裂不及时引起的。除非出现输尿管并发症,否则复制体不会暴露。急性输尿管梗阻不会引起肾功能的明显改变。虽然整个临床表现本身是罕见的,但需要进一步的随访,以避免再次发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Calculus Induced Hydroureteronephrosis Obstructive Syndrome in a Patient with Two Separate Pelvicalcyeal System in Right Side with Bifid Ureter: A Rare Clinical Entity.
Hydroureteronephrosis is a clinical condition where the dilatation of renal calyces and ureter occur jointly due to obstruction. When two ureters arise from single kidney the situation is known as bifid ureter which may be complete orincomplete. The present study examines a congenital anomaly of bifid ureter and rare clinical presentation of calculusinduced obstructive hydroureternephrosis in a adult male aged 38 by past 48 hours. The common symptoms of thiscondition were extreme intolerable pain in the abdomen, flank pain moderate to severe radiate to loin to groin,vomiting/nausea and haematuria. Diagnosis was done by injection of intravenous dye and computed tomographyintravenous pyleogram was performed along with lab findings. In this case we found two incomplete ureters i.e. bifidnature arising from right kidney that unite as a single ureter before emptying into the urinary bladder. There was presence  of single large calculus measuring approximately 8.6*8mm right at the junction of bifid ureter at the level of L3 vertebra  inducing hydroureteronephrosis. Similarly marked upstream dilation of upper right ureter was found. The anomaly of  bifid ureter occurs due to the untimely division of ureteric diverticulum. Unless some complication of ureter occurs, the  duplication does not expose itself. Acute obstruction of ureter does not cause any significant alternation in renal function.  Though the whole clinical presentation is rare itself, it further needs follow ups to avoid re-occurrence.
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