Fetal uropathies: pre- and postnatal imaging, management and follow-up

被引:4
作者
Cassart, Marie [1 ]
机构
[1] Iris South Hosp, Radiol Dept, Site Elterbeek Ixelles,63 Rue Jean Paquot, B-1050 Brussels, Belgium
关键词
Congenital anomalies; Fetus; Kidneys; Postnatal workup; Prenatal ultrasound; Ultrasound; Urinary tract; URINARY-TRACT OBSTRUCTION; MULTICYSTIC DYSPLASTIC KIDNEY; POSTERIOR URETHRAL VALVES; VESICOURETERAL REFLUX; RENAL-FUNCTION; INITIAL MANAGEMENT; ANOMALIES; MRI; ULTRASOUND; DIAGNOSIS;
D O I
10.1007/s00247-022-05433-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Congenital uropathies are the most common fetal anomalies. They include a wide spectrum of anomalies ranging from mild pelvis dilation to complex urinary tract malformations. Prenatal imaging not only allows for their diagnosis but, in experienced hands, it can differentiate obstructive from refluxing or malformative uropathies. Such precise prenatal information allows for intervention before birth in select cases or for adapting the postnatal workup to provide a better long-term outcome. For the different types of congenital uropathies, we describe their prenatal presentations on US and the complementary role of fetal MRI where indicated. We correlate these findings with postnatal workup and summarize the updated neonatal diagnostic and clinical/surgical management.
引用
收藏
页码:610 / 620
页数:11
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