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[先天性巨肾盏症]

[Congenital megacalycosis].

作者信息

Reyes Lara F, Trejo Castillo W

出版信息

Bol Med Hosp Infant Mex. 1982 Jan;39(1):29-31.

PMID:7073878
Abstract

A case of megacalycosis is described in a newborn with multiple anomalies and enlarged kidneys. Uroradiological studies, TAC, ultrasound and nuclear medicine studies were practiced. The excretory urogram was by far the best technique to demonstrate this entity characterized by enlarged kidneys and uniform dilatation of all the calyces with the remainder of the collecting system normal. Voiding cystourethrography was normal as were renal function tests. This rare urological entity is a form of renal dysplasia which must not be confused with obstructive o refluxing hydronephrosis so that needless surgery is avoided.

摘要

本文描述了一例患有多种先天性异常及肾脏增大的新生儿巨肾盏症病例。进行了尿放射学检查、计算机断层扫描(TAC)、超声及核医学检查。排泄性尿路造影是目前显示该病症的最佳技术,其特征为肾脏增大,所有肾盏均匀扩张,而集合系统其余部分正常。排尿性膀胱尿道造影及肾功能检查均正常。这种罕见的泌尿系统病症是肾发育异常的一种形式,切不可与梗阻性或反流性肾积水相混淆,以免进行不必要的手术。

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