Zanini R, Tarantini M, Cerri V, Jacobello C, Bellotti D, Lancetti S, Scalchi S, Groli C, Bianchi U A
Department of Obstetrics and Gynecology, University of Brescia, Italy.
Fetal Diagn Ther. 1998 Mar-Apr;13(2):106-10. doi: 10.1159/000020816.
To evaluate the gestational outcome of pregnancies screen-positive for both neural tube defects (NTD) and Down syndrome (DS) ('dual positivity').
Among 10,667 mid-trimester women screened for DS and NTD with alpha-fetoprotein (AFP), unconjugated estriol (uE3), and human chorionic gonadotropin (hCG), delivered up to July 1996, we have selected cases with both an unexplained AFP value > or = 2.5 multiples of median (MoM) and a DS risk > or = 1:250. All these pregnant women were managed with amniocentesis and/or CVS, ultrasound scans, and Doppler velocimetry. We have collected all data about the gestations with 'dual positivity' and no obvious explanation for these findings (cases with fetal malformations related to raised AFP).
Twelve women (1.1:1,000) showed unexplained 'dual positivity'. Abnormal karyotypes were found in 3 fetuses, and pregnancies were terminated: there were 2 triploidies with partial hydatiform mola, and 1 DS. In 9 cases the fetal karyotype was normal, but a confined placental trisomy 16 was found in 4. Of the 9 continuing gestations, 8 displayed fetal growth retardation (FGR). One gestation ended with fetal death at 27 weeks. All 9 fetuses were morphologically normal, and 8 were small for gestational age.
'Dual positivity' at NTD/DS screening may anticipate pregnancy complications. The finding of trisomy 16 confined to the placenta and FGR in 4 cases suggests that at least some fetuses with growth restriction may suffer from a distinct placental disease. Maternal serum screening may have implications different from DS and NTD, as demonstrated by the 2 cases with triploidy and incomplete hydatiform mola, the 4 cases with placental trisomy 16, and the 4 cases of FGR of the 5 fetuses without chromosome abnormalities. As the pathologic outcome of these pregnancies is more important than the mere serum screening results, we feel that these cases need a strict work-up, including CVS, amniocentesis and ultrasound studies to better address the obstetrical management.
评估神经管缺陷(NTD)和唐氏综合征(DS)筛查均呈阳性(“双重阳性”)的妊娠结局。
在1996年7月前分娩的10667例孕中期妇女中,采用甲胎蛋白(AFP)、游离雌三醇(uE3)和人绒毛膜促性腺激素(hCG)对DS和NTD进行筛查,我们选取了AFP值不明原因地≥2.5倍中位数(MoM)且DS风险≥1:250的病例。所有这些孕妇均接受了羊膜穿刺术和/或绒毛取样、超声扫描及多普勒血流测定。我们收集了所有“双重阳性”妊娠的数据,且对这些结果没有明显解释(与AFP升高相关的胎儿畸形病例)。
12名妇女(1.1:1000)出现不明原因的“双重阳性”。3例胎儿发现核型异常并终止妊娠:2例为部分性葡萄胎三倍体,1例为唐氏综合征。9例胎儿核型正常,但4例发现局限于胎盘的16三体。在9例继续妊娠中,8例出现胎儿生长受限(FGR)。1例妊娠在27周时胎儿死亡。所有9例胎儿形态正常,8例小于孕周。
NTD/DS筛查中的“双重阳性”可能预示妊娠并发症。4例发现局限于胎盘的16三体和FGR表明,至少一些生长受限的胎儿可能患有独特的胎盘疾病。母血清筛查可能具有不同于DS和NTD的意义,如2例三倍体和部分性葡萄胎、4例胎盘16三体以及5例无染色体异常胎儿中的4例FGR所示。由于这些妊娠的病理结局比单纯的血清筛查结果更重要,我们认为这些病例需要严格的检查,包括绒毛取样、羊膜穿刺术和超声检查,以更好地进行产科管理。