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Brillantino, C., Errico, M.E., Minelli, R., Gaglione, G., Pirisi, P., Rossi, A., Menna, B.F., Santarsiere, M., Rumolo, M. and Rossia, E. (2022) Giant Malignant Sacrococcygeal Germ Cell Tumor in a Newborn: A Rare Case Report. Radiology Case Reports, 17, 2416-2423.
https://doi.org/10.1016/j.radcr.2022.03.107

has been cited by the following article:

• TITLE: Sacrococcygeal Teratoma a Rare Tumor in Children: Case Report

  AUTHORS: Hanae Bahari, Hanane Hajaj, Hind Zahiri, Ayyad Ghanam, Aziza El Ouali, Abdeladim Babakhouya, Maria Rkain

  KEYWORDS: Sacrococcygeal Mass, Alpha-Fetoprotein, Surgery

  JOURNAL NAME: Open Journal of Pediatrics, Vol.14 No.1, January 12, 2024

  ABSTRACT: Sacrococcygeal teratomas (SCTs) are uncommon congenital tumors that typically develop in newborns, they are rarely associated with chromosomal abnormalities or other congenital anomalies. The majority of pediatric teratomas are benign in the neonatal age group, but the risk of malignancy increases with age. Diagnosis is based on a combination of clinical, radiological, and hormonal findings, but confirmed by anatomopathological study. Treatment is primarily surgical, with the aim of achieving complete resection to prevent recurrence. We present the case of a 22-month-old child who was admitted for management of a sacrococcygeal mass and was diagnosed with an immature teratoma.