Sacrococcygeal teratoma

Sacrococcygeal teratoma
SpecialtyOncology Edit this on Wikidata

Sacrococcygeal teratoma (SCT) is a type of tumor known as a teratoma that develops at the base of the coccyx (tailbone) and is thought to be primarily derived from remnants of the primitive streak.[1] Sacrococcygeal teratomas are benign 75% of the time, malignant 12% of the time, and the remainder are considered "immature teratomas" that share benign and malignant features. Benign sacrococcygeal teratomas are more likely to develop in younger children who are less than 5 months old, and older children are more likely to develop malignant sacrococcygeal teratomas.

The Currarino syndrome, due to an autosomal dominant mutation in the MNX1 gene, consists of a presacral mass (usually a mature teratoma or anterior meningocele), anorectal malformation and sacral dysgenesis.

  1. ^ Sadler, T. W. (2010). Langman's medical embryology (11th ed.). Philadelphia: Lippincott Williams & Wilkins. p. 63. ISBN 9780781790697.