Unusual lymphangioma observed prenatally in a 45,X fetus

Am J Med Genet. 1993 Feb 15;45(4):508-10. doi: 10.1002/ajmg.1320450421.

Abstract

We present a case of a large frontal lesion, suspected on antenatal ultrasound to be a cephalocele. The cardiac anatomy was abnormal and fetal blood sampling showed a 45,X chromosome constitution. Postmortem examination proved this to be a lymphangioma and confirmed the presence of a cardiac defect. We suggest that this lymphangioma represents an unusual manifestation of monosomy X and discuss the importance of doing chromosome analysis in the presence of such a lesion which is of similar appearance as a cephalocele.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Fetal Diseases / diagnosis
  • Fetal Diseases / diagnostic imaging
  • Fetal Diseases / genetics*
  • Fetal Diseases / pathology
  • Humans
  • Lymphangioma / diagnosis
  • Lymphangioma / diagnostic imaging
  • Lymphangioma / genetics*
  • Lymphangioma / pathology
  • Monosomy*
  • Pregnancy
  • Prenatal Diagnosis*
  • Scalp
  • Skin Neoplasms / diagnosis
  • Skin Neoplasms / diagnostic imaging
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / pathology
  • Ultrasonography
  • X Chromosome*