- Etiology: Presacral germ cell tumor consisting of totipotential cells of Hensen’s node (caudal cell mass migrates anteriorly to coccyx)
- Types: Based on location in relationship to pelvis
— Type I mainly external with small presacral component
— Type II external presentation with large intrapelvic component
— Type III external component with majority of tumor in pelvis and abdomen
— Type IV entirely presacral without externally visible component - Imaging:
— Mass is cystic or solid or mixed
— May have increased vascularity
— May have calcification - DDX: Presacral mass
- Complications: May transform into malignancy
- Treatment: Surgical
- Clinical:
— Sacrococcygeal region is most common site for teratomas in CNS
— AFP elevated
— Most common solid tumor in neonates
— Most common congenital neoplasm
— 90% benign at birth
— Can present with high output congestive heart failure
— May have hydrops fetalis particularly when solid
— May be part of Currarino triad
— Often associated with other abnormalities including anorectal and genital malformations, ventricular septal defect, hip dislocation, vertebral anomalies (spina bifida, sacral agenesis)
Radiology Cases of Sacrococcygeal Teratoma


Clinical Cases of Sacrococcygeal Teratoma


Gross Pathology Cases of Sacrococcygeal Teratoma




Histopathology Cases of Sacrococcygeal Teratoma
