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.
Taibi et al. (Sun,) studied this question.