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首页> 外文期刊>Urology Annals >Posterior urethral valve with unilateral vesicoureteral reflux and patent urachus: A rare combination of urinary tract anomaliess
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Posterior urethral valve with unilateral vesicoureteral reflux and patent urachus: A rare combination of urinary tract anomaliess

机译:后尿道瓣膜单侧膀胱输尿管反流和漆器性天疱疮:尿路异常的罕见组合

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摘要

Posterior urethral valve (PUV) is a common cause of lower urinary tract obstruction in male infants with an incidence of 1:5000-8000. PUV continues to be a significant cause of morbidity and ongoing renal damage in infants and children. It can coexist with vesicoureteral reflux (VUR) in about 50% of cases and also with patent urachus in about one-third of cases. It is a case of a 22-day-old full-term male child who presented with poor urinary stream and progressive abdominal distension of 5-day duration as well as leakage of clear fluid from umbilicus of 1-day duration. Abdominopelvic ultrasonography showed bilateral hydronephrosis. Micturating cystourethrogram also showed features of bladder outlet obstruction and PUV. In addition, a grade V left VUR and a fistulous tract between the dome of the urinary bladder and the umbilicus, which was consistent with a patent urachus was demonstrated. In conclusion, this case demonstrates a rare combination of congenital urinary tract anomalies involving PUV, left VUR and patent urachus.
机译:后尿道瓣膜(PUV)是男性婴儿下尿路梗阻的常见原因,发生率1:5000-8000。 PUV仍然是婴儿和儿童发病率和持续肾脏损害的重要原因。它可以在约50%的病例中与膀胱输尿管反流(VUR)共存,并且在约三分之一的病例中与乌拉圭专利共存。这是一个22岁的足月男婴的情况,其尿流较差,进行性腹胀持续时间为5天,并且清液从持续1天的脐带中渗出。腹腔超声检查显示双侧肾盂积水。膀胱尿道造影也显示膀胱出口梗阻和PUV。此外,还证实了V级左VUR和膀胱穹顶与脐部之间的瘘管,这与漆皮小盲肠是一致的。总而言之,该病例说明了罕见的先天性尿道异常,包括PUV,左VUR和漆皮红肿。

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