M. Locci et al., CORRELATION OF DOPPLER AND PLACENTAL IMMUNOHISTOCHEMICAL FEATURES IN NORMAL AND INTRAUTERINE GROWTH-RETARDED FETUSES, Ultrasound in obstetrics & gynecology, 3(4), 1993, pp. 240-245
Citations number
NO
Categorie Soggetti
Acoustics,"Obsetric & Gynecology","Radiology,Nuclear Medicine & Medical Imaging
The aim of this study was to correlate and compare Doppler and anatomi
cal placental findings obtained from 48 normal and 35 intrauterine gro
wth-retarded (IUGR) fetuses. The IUGR group consisted of 19 fetuses fr
om pregnancies complicated by pre-eclampsia and 16 from healthy mother
s. Color Doppler evaluation of umbilical, spiral and uterine arteries
was performed Placental specimens from both normal and growth-retarded
fetuses were obtained at the time of delivery. Placental specimens we
re evaluated using histochemical and immunohistochemical techniques. A
progressive decrease in the pulsatility index was observed in umbilic
al, spiral and uterine arteries throughout pregnancy in the normal-gro
wth fetuses. High umbilical artery pulsatility index values were obtai
ned in 29 out of the 35 growth-retarded fetuses, six of them showing a
bsent or reversed end-diastolic umbilical artery flow pattern. A total
of 13 IUGR fetuses showed high resistance uterine artery flow velocit
y waveforms. Increased pulsatility index values were obtained from the
spiral arteries of 16 growth-retarded fetuses. Abnormal histological
and histochemical placental patterns were observed in all the growth-r
etarded fetuses with umbilical artery Doppler abnormalities. The prese
nce of a peculiar dendritic cell subpopulation, strongly resembling th
e Langerhans cells, expressing the HLA-DR+/CD1+ phenotype, was detecte
d in all growth-retarded fetuses, whether there was maternal pathology
or not. Our data show uterine and spiral artery data as being ineffec
tive in the monitoring of IUGR fetuses. The placental extracellular ma
trix seems to play an important role in the regulation of the umbilica
l circulation. The presence of CD1+ cells as a sign of a possible immu
nological mechanism in the pathogenesis of the intrauterine growth ret
ardation is discussed.