Prenatally diagnosed sacrococcygeal teratoma: a unique expression of trisomy 1q

Cancer Genet Cytogenet. 2000 Feb;117(1):84-6. doi: 10.1016/s0165-4608(99)00141-7.

Abstract

Partial duplication of the long arm of chromosome 1 has been observed in fetal intracranial teratomas. We sonographically diagnosed a 19-week fetus with sacrococcygeal teratoma, cerebral ventriculomegaly, and cerebellar hypoplasia. Chromosomal analysis of amniocytes showed an unbalanced translocation between chromosomes 1 and 15, resulting in trisomy 1q21-->1 qter. Duplication or over expression at more than one locus on the long arm of chromosome 1 may be required for the development of an extra-gonadal teratoma.

MeSH terms

  • Female
  • Fetal Diseases / diagnostic imaging*
  • Fetal Diseases / genetics
  • Humans
  • Karyotyping
  • Pregnancy
  • Sacrococcygeal Region / pathology*
  • Teratoma / diagnostic imaging*
  • Teratoma / genetics
  • Ultrasonography, Prenatal