Abstract:Blind-ending bifid ureter in a woman with urinary tract infection and a duplicated renal pelvis in her twin sister are reported. The blind-ending bifid ureter terminated as a fibrous cord with a terminal mass of immature renal tissue. This type of ureter may be a transitional form between histologically blind-ending bifid ureter and duplication of the renal pelvis and/or kidneys. Findings in twins support this opinion.
“…The majority of duplication anomalies affect females (female:male 3:1) and can be genetically inherited showing concordance [3,4]. Symptoms can include those of infection and calculi but are often ill-defined presenting as non-specific chronic flank pain, colic or vague abdominal pain most often affecting the right side [5].…”
“…The majority of duplication anomalies affect females (female:male 3:1) and can be genetically inherited showing concordance [3,4]. Symptoms can include those of infection and calculi but are often ill-defined presenting as non-specific chronic flank pain, colic or vague abdominal pain most often affecting the right side [5].…”
Blind-ending bifid ureter in a girl with urinary tract infection, and a blind-ending duplicated ureter in her younger sister are described. The embryology of this rare anomaly is briefly reviewed.
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