PC-GG18 : Currarino Syndrome in an Adult Woman: A Case Report

Currarino syndrome is a rare autosomal dominant hereditary disorder and presents a triad that consists of partial sacral dysgenesis, presacral mass and anorectal malformation. Mutation of a homeobox gene, HLXB9 is the major cause in Currarino syndrome. Its clinical presentations are variable such as imperforate anus at birth, persistent constipation from anorectal stenosis, presacral mass, or acute meningitis. We report a 29-year-old female patient diagnosed with Currarinos triad. The patient visited the gynecologic clinic because of suspected pelvic mass.