It was first described in the paediatric population with treated germ cell neoplasms, and represents enlarging masses at the site of previous tumour deposits. It is often cystic, and occurs after complete serological response to multimodality therapy.
The enlarging tumour consists of mature tissues from all three layers (endoderm, mesoderm and ectoderm) thus representing a mature teratoma, that presumably arises from differentiated cells that are refractory to chemotherapy or radiation.
The incidence systemically is estimated between 1.9 and 7.6% and is most often seen in the retroperitoneum in patients with metastatic testicular non-seminomatous germ cell tumours.
- 1. Bi WL, Bannykh SI, Baehring J. The growing teratoma syndrome after subtotal resection of an intracranial nongerminomatous germ cell tumor in an adult: case report. Neurosurgery. 2006;56 (1): 188. Pubmed citation
- 2. O'Callaghan AM, Katapodis O, Ellison DW et-al. The growing teratoma syndrome in a nongerminomatous germ cell tumor of the pineal gland: a case report and review. Cancer. 1997;80 (5): 942-7. Pubmed citation