An unusual urinary tract presentation in a case of megacystis microcolon intestinal hypoperistalsis syndrome.

[megacystis-microcolon-intestinal hypoperistalsis syndrome]

Megacystis microcolon intestinal hypoperistalsis syndrome is a rare congenital anomaly . Several pathogeneses have been described so far , but there is no single mechanism that can explain all the findings of the syndrome . Affected newborns usually present clinically in the first few days of life . The mainstay of diagnosis is a pre or a postnatal imaging evaluation using ultrasound or magnetic resonance imaging . We report an unusual urinary tract finding in a patient with the classic triads of the syndrome that was diagnosed with both pre and postnatal imaging evaluation .