Spontaneous rupture of fetal sacrococcygeal teratoma

Chun Wei Shih, Hanmin Lee, Robert Ball, Jody Farrell, Liina Poder, Kerilyn K. Nobuhara, Diana L. Farmer, Michael R. Harrison

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)


With recent advances in technology, fetal sacrococcygeal teratoma is being diagnosed increasingly during the early prenatal period by ultrasound examination. In addition, early detection of tumor related complications such as polyhydramnios, congestive heart failure, hydrops, hemorrhage, urinary tract or bowel obstruction can be followed closely in utero. Active prenatal management can improve fetal perinatal outcome by allowing planned delivery for neonatal surgery [Chisholm, C.A. et al.: Am J Perinatol 1999;16:47-50] or in some cases, fetal intervention. Additionally, families can be counseled appropriately regarding the range of outcomes. We report a case of fetal sacrococcygeal teratoma Type I diagnosed at 20 weeks with a prominent vessel supplying the tumor mass. At 23 weeks, there was a sudden appearance of an additional lobular mass, consistent with intrauterine spontaneous ruptured of a sacrococcygeal teratoma mass.

Original languageEnglish
Pages (from-to)424-427
Number of pages4
JournalFetal Diagnosis and Therapy
Issue number5
Publication statusPublished - 2006 Aug 1

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Embryology
  • Radiology Nuclear Medicine and imaging
  • Obstetrics and Gynaecology

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