Fœtal sacrococcygeal teratoma type I: A case report

Bibliographic Details
Title: Fœtal sacrococcygeal teratoma type I: A case report
Authors: Haithem Aloui, MD, Eya Azouz, MD, Hatem Frikha, MD, Hammami Rami, MD, Douha Aoun, MD, Neila Ben Aba, MD, Ayeb Saad, MD, Yasmine Houas, MD, Riadh jouini, MD
Source: Radiology Case Reports, Vol 20, Iss 2, Pp 920-923 (2025)
Publisher Information: Elsevier, 2025.
Publication Year: 2025
Collection: LCC:Medical physics. Medical radiology. Nuclear medicine
Subject Terms: Teratoma, Sacrococcygeal, Foetus, Medical physics. Medical radiology. Nuclear medicine, R895-920
More Details: Sacrococcygeal teratoma (SCT) is a rare congenital tumor typically diagnosed in neonates, with management challenges arising from the size of the tumor and associated delivery complications. In this case, a 32-year-old gravida 5 para 5 woman with a history of three prior cesarean sections was diagnosed with a giant type I SCT at 30 weeks of gestation through prenatal ultrasound, confirmed by fetal MRI. At 34 weeks, an emergency cesarean section was performed due to acute fetal distress, resulting in a newborn with transient respiratory distress. Postnatal imaging classified the tumor as type I SCT, and it was successfully excised on the third day of life without complications. The patient recovered well and was discharged on day fifteen. This case highlights the importance of early prenatal diagnosis, surgical intervention, and multidisciplinary care in managing large SCTs.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1930-0433
Relation: http://www.sciencedirect.com/science/article/pii/S1930043324012251; https://doaj.org/toc/1930-0433
DOI: 10.1016/j.radcr.2024.10.120
Access URL: https://doaj.org/article/9fccdd52987e4066b54ae031d0090362
Accession Number: edsdoj.9fccdd52987e4066b54ae031d0090362
Database: Directory of Open Access Journals
More Details
ISSN:19300433
DOI:10.1016/j.radcr.2024.10.120
Published in:Radiology Case Reports
Language:English