{Reference Type}: Case Reports
{Title}: Currarino triad: A case report of a 48-year-old patient with a neuroendocrine tumor.
{Author}: Rebelo J;Marques A;Vilares T;Silva N;Silva R;Cunha R;Madureira A;
{Journal}: Radiol Case Rep
{Volume}: 15
{Issue}: 9
{Year}: Sep 2020
暂无{DOI}: 10.1016/j.radcr.2020.06.039
{Abstract}: Currarino triad is a rare syndrome, with less than 250 cases reported, and it includes a combination of sacrococcigeal bony abnormalities, anorectal malformations and the presence of a presacral mass. Here we present a case of a 48-year-old male patient with history of severe chronic constipation, who was incidentally diagnosed with a presacral during imagiological investigation, which was histologically proven to be a neurendocrine tumor.