Spontaneous rupture of fetal sacrococcygeal teratoma

Edgar D. Sy, Hanmin Lee, Robert Ball, Jody Farrell, Liina Poder, Kerilyn K. Nobuhara, Diana L. Farmer, Michael R. Harrison

研究成果: Article同行評審

9 引文 斯高帕斯(Scopus)

摘要

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.

原文English
頁(從 - 到)424-427
頁數4
期刊Fetal Diagnosis and Therapy
21
發行號5
DOIs
出版狀態Published - 2006 8月

All Science Journal Classification (ASJC) codes

  • 兒科、圍產兒和兒童健康
  • 胚胎學
  • 放射學、核子醫學和影像學
  • 婦產科

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