Abstract
Purpose
Isolated classic bladder exstrophy (CBE) is the most common variant of the bladder-exstrophy–epispadias complex (BEEC). The BEEC represents a spectrum ranging from isolated epispadias over CBE to the most severe form, cloacal exstrophy. We report on a series of 12 cases with CBE diagnosed prenatally and illustrate the spectrum of prenatal ultrasound findings with comparison to prior published reports on this entity.
Methods
This was a retrospective study involving 12 fetuses with CBE at two large tertiary referral centers in Germany over a 14-year period (2004–2018).
Results
Median diagnosis was made with ultrasound in 24 + 5 (IQR25,75: 21 + 2, 29 + 0) weeks of gestation. All fetuses presented with the pathognomonic findings non-visualization of the fetal bladder and protruding abdominal mass below the umbilical cord insertion. All fetuses showed normal kidney anatomy and normal amniotic fluid throughout pregnancy. Epispadia was visible prenatally on ultrasound in 6/8 male fetuses. 1/12 Parents opted for termination of pregnancy, 11/12 fetuses were live born and received reconstructive surgery.
Conclusions
Isolated CBE is an extremely rare prenatal sonographic finding. Prenatal diagnostics should exclude additional malformations within the spectrum of cloacal malformations.
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MRM: project development, data collection, data analysis, manuscript writing. BM-D: data collection, data analysis. HR: data analysis, data analysis, manuscript writing. RP: data collection, manuscript editing. IG: data collection, data analysis, manuscript editing. AG: data collection, data analysis, manuscript editing. CB: data collection, data analysis, manuscript editing. TMB: project development, data collection, manuscript writing. UG: project development, data collection, data analysis, manuscript writing. All authors finally approved the manuscript.
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Mallmann, M.R., Mack-Detlefsen, B., Reutter, H. et al. Isolated bladder exstrophy in prenatal diagnosis. Arch Gynecol Obstet 300, 355–363 (2019). https://doi.org/10.1007/s00404-019-05193-x
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DOI: https://doi.org/10.1007/s00404-019-05193-x