In this study, we have determined the increasing rate of detection of
cystic hygroma in an urban hospital-based Active Malformations Surveil
lance Program during 1973-1974, 1979-1980, 1984-1985, and 1989-1990, A
l affected infants were identified from a review of the findings in ei
ther the findings in the pediatricians' examinations, the autopsy repo
rts or the reports of finding in prenatal ultrasonography. The infants
were subdivided by maternal transfer status and age (greater than or
equal to 5 or <35), the presence of associated chromosome abnormalitie
s and malformations and birth status. Eighty-four affected infants and
fetuses were identified, 47 of whose mothers were nontransfers. Among
the maternal nontransfers, the prevalence rate of cystic hygroma incr
eased from 0.08/1,000 in 1973-1974 to 1.45/1,000 in 1988-1990. Initial
ly, the diagnosis was made at birth in liveborn or stillborn infants,
but by 1989-1990, only by prenatal ultrasonography. Most (71%) of the
pregnancies with affected fetuses were terminated by choice following
diagnosis with prenatal ultrasonography. A marked increase in the freq
uency of examination by sonography during pregnancy was observed among
a comparison group of women between 1974 and 1989. The progressive in
crease in the detection of cystic hygroma in this time period was one
effect of this more extensive use of prenatal ultrasound, better equip
ment, and more experienced sonographers. (C) 1997 Wiley-Liss, Inc.