Congenital cystic hygroma of the neck diagnosed prenatally: outcome with normal and abnormal karyotype

Prenat Diagn. 1989 May;9(5):321-7. doi: 10.1002/pd.1970090504.

Abstract

Twenty-two cases of cystic hygromas were diagnosed prenatally at Eastern Virginia Medical School and followed through the neonatal period. Our series was combined with 131 cases which have been described in the literature. Karyotypes were obtained in 110 fetuses and 80 (72.7 per cent) were abnormal. Fifty-one were not terminated: 30 with abnormal and 21 with normal karyotypes. There were no neonatal survivors in the group with abnormal karyotypes. There were five survivors in the 21 with normal karyotypes but only 2/21 without severe medical complications. Combining our series with those previously reported in the literature would suggest only a 2-3 per cent rate of intact survivors when fetal cystic hygromas are diagnosed in utero. This information should be helpful when counselling patients whose pregnancies carry this diagnosis.

Publication types

  • Review

MeSH terms

  • Amniotic Fluid / cytology
  • Female
  • Head and Neck Neoplasms / congenital*
  • Head and Neck Neoplasms / diagnosis*
  • Head and Neck Neoplasms / mortality
  • Humans
  • Hydrops Fetalis / diagnosis
  • Karyotyping
  • Lymphangioma / congenital*
  • Lymphangioma / diagnosis*
  • Lymphangioma / mortality
  • Pregnancy
  • Prenatal Diagnosis*
  • Prognosis
  • Ultrasonography