Case Report
A brief case report of duplicated bladder exstrophy: A congenital malformation in paediatrics
Author(s): Suleyman Tagci*, Gokhan Demırtas, Derya Yayla, Bilge Karabulut and Huseyin Tugrul Tiryaki
Duplicated bladder exstrophy is an extremely rare variant of the exstrophy/epispadias complex. We present
two rare case of duplicate exstrophy with a wet and dry bladder plate. A rare congenital malformation
is duplicate bladder exstrophy. The anteroposterior form has been described, as has the collateral form,
which is the less common. A case of bladder exstrophy with a duplicated lower urinary tract, omphalocele,
colic duplication, and diphallia is described.
Due to the inability to identify the ureteral orifices during surgical repair, a normally positioned external
urethral meatus joined a closed bladder posterior to the exstrophic one. Both ureteric orifices opened into
the closed bladder’s thin distensible wall. There was recti divergence and diastases of the pelvic bones. Because
the exstrophic wall was the only muscular component, it was deci.. Read More»
DOI:
10.14534/j-pucr.20222675574