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Antenatally detected urinary tract dilatation: a pediatric nephrologist's point of view

Authors :
Hyung Eun Yim
Source :
Childhood Kidney Diseases, Vol 28, Iss 1, Pp 1-7 (2024)
Publication Year :
2024
Publisher :
Korean Society of Pediatric Nephrology, 2024.

Abstract

Antenatally diagnosed urinary tract dilatation (UTD), previously referred to as antenatal hydronephrosis, is the most commonly detected abnormality by prenatal ultrasonography. Several grading systems have been developed for the classification of antenatal UTD using prenatal and postnatal ultrasonography. UTD comprises a wide variety of congenital abnormalities of the kidney and urinary tract ranging from transient UTD to more significant abnormalities such as vesicoureteral reflux, ureteropelvic junction obstruction, ureterocele, ureterovesical junction obstruction, posterior urethral valves, and non-refluxing megaureter. Optimizing the evaluation of antenatally detected UTD is essential to recognize children with important disorders while avoiding excessive investigations. Conservative approach with close follow-up is increasingly accepted as an appropriate treatment option for patients with asymptomatic vesicoureteral reflux and ureteropelvic junction obstruction in recent years. However, predicting permanent kidney damage in an unselected group of children with antenatal UTD is still challenging. The management and follow-up of children with UTD should be individualized based on recommendations from a pediatric nephrologist, a pediatric urologist, or both. Future research directed at predicting long-term outcomes of children diagnosed with UTD from mild findings to severe disease is needed to refine management for those at higher risk of kidney disease progression.

Details

Language :
English
ISSN :
23840242 and 23840250
Volume :
28
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Childhood Kidney Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.7abf761b8411438fa609bd2de16a3971
Document Type :
article
Full Text :
https://doi.org/10.3339/ckd.24.002