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Published on: September 22, 2023
[DISTENDED FETAL BLADDER].
Dana Shapira1,2, Roxana Cleper1,2
1Pediatric Nephrology Unit, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center.
Fetal megacystis, or distended fetal bladder, can stem from primary vesicoureteral reflux (VUR), leading to kidney issues. Isolated cases without other abnormalities often resolve post-birth.
Area of Science:
- Fetal medicine
- Pediatric urology
- Neonatal nephrology
Background:
- Distended fetal bladder (fetal megacystis) typically indicates lower urinary tract obstruction (LUTO), commonly posterior urethral valves (PUV) in males.
- Posterior urethral valves (PUV) are the most frequent cause of LUTO, often leading to significant fetal urinary tract abnormalities.
Purpose of the Study:
- To investigate fetal megacystis cases where primary vesicoureteral reflux (VUR) is the primary cause, not LUTO.
- To analyze the association between fetal megacystis, kidney dysplasia, renal dysfunction, and neurodevelopmental outcomes.
Main Methods:
- Retrospective case-series analysis of fetal megacystis diagnosed prenatally.
- Evaluation of postnatal outcomes, including renal function, spontaneous resolution, and neurodevelopmental assessments.
- Genetic and imaging evaluations for extra-renal malformations.
Main Results:
- Primary VUR was identified as a significant cause of fetal megacystis without oligohydramnion.
- Cases with primary VUR showed high rates of kidney dysplasia and early renal dysfunction.
- Isolated fetal megacystis without significant renal abnormalities had a benign postnatal course with spontaneous resolution.
Conclusions:
- Primary VUR is an important etiology of fetal megacystis, often associated with renal dysplasia and dysfunction.
- Isolated fetal megacystis may have a favorable prognosis, resolving spontaneously after birth.
- Associated extra-renal and neuro-cognitive abnormalities necessitate thorough genetic and imaging evaluation.
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