正常、贫血、小、三体和三倍体胎儿的平均红细胞体积。

Fetal therapy Pub Date : 1989-01-01 DOI:10.1159/000263384
K H Nicolaides, R J Snijders, J G Thorpe-Beeston, M C Van den Hof, C M Gosden, A J Bellingham
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引用次数: 24

摘要

通过对466例产前诊断为非红细胞异常的孕妇进行脐带穿刺取样的研究,建立了妊娠期胎儿平均红细胞体积(MCV)的参考范围。平均MCV从妊娠16周时的145 fl降至妊娠36周时的113 fl。研究人员在154例红细胞等免疫和231例小胎龄(SGA)胎儿中研究了MCV的变化。在红细胞等免疫中,当胎儿血红蛋白浓度缺陷大于或等于6 g/dl时,观察到明显的巨噬细胞增多。在染色体正常的SGA胎儿(n = 178)中,MCV升高,巨噬细胞增多的程度与妊娠、胎儿“小”和胎儿低氧血症的程度显著相关。然而,最严重的SGA大细胞增生胎儿是三倍体胎儿(n = 22)。在有其他染色体缺陷的SGA胎儿(n = 31)中,MCV高于对照组,但低于染色体正常的低氧血症胎儿。这表明在严重的生长迟缓中存在着从肝脏造血到髓质造血的正常进化的发育迟缓,这在三倍体胎儿中最为明显。相反,在红细胞等免疫中,向髓质红细胞生成的转变是正常的,但在严重贫血中,有继发性肝红细胞生成的补充。
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Mean red cell volume in normal, anemic, small, trisomic and triploid fetuses.

A reference range for fetal mean red cell volume (MCV) with gestation was established from the study of samples obtained by cordocentesis from 466 pregnancies undergoing prenatal diagnosis for non-erythrocyte abnormalities. The mean MCV decreased from 145 fl at 16 weeks to 113 fl at 36 weeks of gestation. Alterations in MCV were investigated in 154 red cell isoimmunized and 231 small for gestational age (SGA) fetuses. In red cell isoimmunization, significant macrocytosis was observed when the fetal hemoglobin concentration deficit was greater than or equal to 6 g/dl. In the chromosomally normal SGA fetuses (n = 178), the MCV was increased and the magnitude of macrocytosis was significantly associated with gestation and the degrees of fetal 'smallness' and fetal hypoxemia. However, the most severely macrocytotic SGA fetuses were those with triploidy (n = 22). In the SGA fetuses with other chromosomal defects (n = 31), the MCV was higher than the controls but lower than that of the chromosomally normal hypoxemic fetuses. It is suggested that in severe growth retardation there is developmental delay in the normal evolution from hepatic to medullary hemopoiesis and this is most marked in triploid fetuses. In contrast, in red cell isoimmunization the switch to medullary erythropoiesis is normal, but in severe anemia there is secondary recruitment of hepatic erythropoiesis.

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