Sacrococcygeal Teratoma: A 12-Year Experience Of A Single Center

Original Article

Sacrococcygeal Teratoma

  • Fatma Tuğba GÜVENÇ Dr. Sami Ulus Maternity and Children’s Hospital
  • Burak ARDIÇLI Dr. Sami Ulus Maternity and Children’s Hospital
  • İbrahim KARAMAN Dr. Sami Ulus Maternity and Children’s Hospital
  • Derya ERDOĞAN Dr. Sami Ulus Maternity and Children’s Hospital
  • Engin YILMAZ Dr. Sami Ulus Maternity and Children’s Hospital
  • Haşim Ata MADEN Dr. Sami Ulus Maternity and Children’s Hospital
  • Ayşe KARAMAN Dr. Sami Ulus Maternity and Children’s Hospital
  • İsmet Faruk ÖZGÜNER Dr. Sami Ulus Maternity and Children’s Hospital

Abstract

Objective: Sacrococcygeal tumor is a rare benign or malign germ cell tumor of infancy and early childhood. We report a 12-year single-center experience. Patients and method: A total of 16 children with operated sacrococcygeal teratoma from 2004 to 2016 were reviewed retrospectively for their clinical features, treatment and follow-up. Results: There were five boys and eleven girls between 1 day to 4 years of age. The most common symptom was sacrococcygeal mass. Complete resection of tumor involving coccyx was performed in all patients. Recurrence was seen in one case. Metastasis was also seen in one case. Conclusion: Sacrococcygeal tumor is the most common tumor in newborn. Total excision is the treatment. The prognosis is excellent despite large tumor size and local invasion.

Downloads

Download data is not yet available.
Published
Jun 30, 2017
How to Cite
GÜVENÇ, Fatma Tuğba et al. Sacrococcygeal Teratoma: A 12-Year Experience Of A Single Center. Acta Medica, [S.l.], v. 48, n. 2, p. 1-5, june 2017. ISSN 2147-9488. Available at: <https://actamedica.org/index.php/actamedica/article/view/67>. Date accessed: 18 nov. 2017.
Section
Original Article