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Currarino Syndrome with Associated Uterine Malformation: A Case Report
Ouiam Taibi1, Soufiane Hassar1, Rania Bouanane1
1Mohammed V University of Rabat, Morocco.
None:
Currarino syndrome (CS), also known as the Currarino triad, is a rare congenital condition characterized by sacral agenesis, anorectal malformation, and a presacral mass. Most cases are diagnosed in childhood, although associations with Müllerian duct anomalies have been occasionally reported. We report a case of late diagnosis of Currarino syndrome revealed by an infectious complication of a presacral mass. The patient had undergone surgery for anal stenosis during infancy, without further evaluation for an underlying syndromic condition. In addition, this case was associated with a uterine malformation, further highlighting its diagnostic complexity.
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