A case report of placental mesenchymal dysplasia with an increased VEGF-D expression

Placenta. 2012 Oct;33(10):888-91. doi: 10.1016/j.placenta.2012.07.015. Epub 2012 Aug 4.

Abstract

The pathogenesis of placental mesenchymal dysplasia (PMD) remains unclear. This report presents a case of PMD with a female fetus complicated with intrauterine growth restriction (IUGR). The ultrasound findings were similar to molar pregnancies, but PMD was suspected based on the presence of low β-hCG levels and a normal karyotype. After delivery, pathological examination of the placenta showed dilated villi and thick-walled vessels lacking trophoblast proliferation, which thus led to a diagnosis of PMD. The VEGF-D (Xp22.31) mRNA expression was found to have increased in the abnormal villi. Whether this is an incidental or X-linked gene specific event in, IUGR complicated, PMD pathogenesis warrants further investigation of VEGF-D expression in PMD.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chorionic Gonadotropin, beta Subunit, Human / analysis
  • Diagnosis, Differential
  • Female
  • Fetus / pathology
  • Humans
  • Hydatidiform Mole / diagnosis
  • Placenta / pathology
  • Placenta Diseases / diagnostic imaging
  • Placenta Diseases / pathology
  • Placenta Diseases / physiopathology*
  • Pregnancy
  • Ultrasonography
  • Vascular Endothelial Growth Factor D / biosynthesis*

Substances

  • Chorionic Gonadotropin, beta Subunit, Human
  • Vascular Endothelial Growth Factor D