ArticleClinical case reports2026
Giant Fetal Sacrococcygeal Teratoma: Prenatal Detection, Monitoring, and Postnatal Management-A Case Report and Literature Review.
Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Sacrococcygeal teratoma (SCT) is a rare congenital tumor arising from pluripotent cells at the base of the coccyx and is most often detected during antenatal imaging. In this case, a massive SCT was identified at 26 + 2 weeks during routine ultrasound. The pregnancy was closely monitored with serial scans; however, the mother went into spontaneous preterm labor at 33 weeks and underwent emergency cesarean section. The neonate had an Altman Type I SCT, which was surgically excised on the fourth day of life, and histopathology confirmed a mature cystic teratoma. Postoperative wound infection was managed conservatively with antibiotics, resulting in good clinical outcomes over a 4-month and 10 month follow-up period. This case highlights the importance of early antenatal detection, timely surgical intervention, and coordinated multidisciplinary care in achieving favorable outcomes for congenital SCT, even in resource-limited settings.
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