Merrot T, Chaumoitre K, Panuel M, Alessandrini P
Unité d'Urologie Pédiatrique, CHU Nord, Université de la Méditerranée, Marseille, France.
Prog Urol. 1999 Sep;9(4):734-8.
The authors report three cases of antenatally diagnosed polycystic renal dysplasia (PRD) associated with homolateral anomalies of the ureter and vas deferens requiring surgical exploration. The antenatal and postnatal diagnosis of polycystic renal dysplasia is based on ultrasound. It is recommended to look for associated vesicoureteric reflux by retrograde cystography. Conservative management is advised due to the natural involution of PRD. The authors emphasize the need for a more detailed ultrasound analysis of the lower genitourinary tract during the antenatal and postnatal period in order to identify an abnormal ureteric orifice, constituting the cause of the dysplasia. As dysplasia is predominant and the only anomaly detected on the antenatal examination, the associated lower tract anomalies will probably only be identified at birth. A better understanding and neonatal detection of associated lower urinary tract malformations probably justify a review of the current, systematic conservative approach, in a certain number of cases.
作者报告了三例产前诊断为多囊性肾发育不良(PRD)的病例,这些病例伴有同侧输尿管和输精管异常,需要进行手术探查。多囊性肾发育不良的产前和产后诊断基于超声检查。建议通过逆行膀胱造影寻找相关的膀胱输尿管反流。由于PRD会自然消退,建议采取保守治疗。作者强调,在产前和产后期间,需要对下泌尿生殖道进行更详细的超声分析,以识别构成发育不良原因的异常输尿管口。由于发育不良占主导地位且是产前检查中唯一检测到的异常,相关的下尿路异常可能仅在出生时才能发现。对相关下尿路畸形有更好的了解并在新生儿期进行检测,可能在某些情况下证明有必要对当前系统的保守方法进行重新审视。