Evaluation of prenatally diagnosed fetal sacrococcygeal teratomas: A case series of seventeen pregnancies from south-central turkey Prenatal dönemde tanı konulan sakrokoksigeal teratomlu fetüslerin değerlendirilmesi: Doğu akdeniz bölgesinden on yedi gebelik olgu serisi


Özsürmeli M., BÜYÜKKURT S., SUCU M., ARSLAN E., Mısırlıoğlu S., Akçabay Ç., ...Daha Fazla

Turkish Journal of Obstetrics and Gynecology, cilt.17, sa.3, ss.170-174, 2020 (ESCI, Scopus, TRDizin)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 17 Sayı: 3
  • Basım Tarihi: 2020
  • Doi Numarası: 10.4274/tjod.galenos.2020.68812
  • Dergi Adı: Turkish Journal of Obstetrics and Gynecology
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.170-174
  • Anahtar Kelimeler: Prenatal diagnosis, teratoma, sacrococcygeal region
  • Sağlık Bilimleri Üniversitesi Adresli: Evet

Özet

Objective: To evaluate sacrococcygeal teratoma (SCT) cases according to associated cardiac, extracardiac, and chromosomal anomalies in the prenatal period, and to review their outcomes. Materials and Methods: Data of pregnancies with a prenatal diagnosis of SCT between 2009 and 2019 were retrospectively reviewed. Results: One ongoing pregnancy was excluded. There were five medically terminated cases, three due to severe heart failure and the remaining two due to additional congenital defects. Two infants who had heart failure due to hyperdynamic flow died in the neonatal period. Nine infants are well and alive at the time of writing. Conclusion: When a lesion is detected in the sacrococcygeal region during fetal sonography, the differential diagnosis should be made with an appropriate evaluation with emphasis on a possible diagnosis of fetal SCT. Tumor growth and heart failure should be monitored with serial scans when SCT has been diagnosed prenatally.