[Are there genetic risk factors in the occurrence of choriocarcinoma?]

Geburtshilfe Frauenheilkd. 1985 Feb;45(2):103-6. doi: 10.1055/s-2008-1036215.
[Article in German]

Abstract

Now that we know about the genetic production mechanisms of diseases of the trophoblast, interest is concentrated on the question which risk factors can produce a disposition in the patient - seen from a clinico-genetic angle - towards malignancy of a complete mole. Many years before the genetic interrelations became known, there had been discussions on blood relationship as a possible aetiological factor in the production of chorionic carcinoma. Since consanguinity in preceding generations can lead to a selection of certain genotypes, this question was reexamined on a limited patients material (10 patients with chorionic carcinoma and 11 with mole). The negative result of this study contradicts - similar to other recent publications on this subject - the hitherto frequently advanced hypothesis that homozygotism is responsible, for a recessive "onko" gen, for rendering a complete mole malignant. Recent investigations, for example, point to a close correlation between the presence of a Y chromosome in a complete mole, and malignancy.

Publication types

  • English Abstract

MeSH terms

  • Choriocarcinoma / genetics*
  • Female
  • Gene Expression Regulation
  • Genes, Recessive
  • Genotype
  • Humans
  • Hydatidiform Mole / genetics
  • Karyotyping
  • Male
  • Pregnancy
  • Risk
  • Turner Syndrome / genetics
  • Uterine Neoplasms / genetics*
  • Y Chromosome