Ulm B, Ulm M R, Deutinger J, Bernaschek G
Department of Obstetrics and Gynecology, University Hospital of Vienna, Austria.
Ultrasound Obstet Gynecol. 1997 Sep;10(3):167-70. doi: 10.1046/j.1469-0705.1997.10030167.x.
This study examined rates of concomitant structural and chromosomal abnormalities in 14 fetuses with a diagnosis of Dandy-Walker malformation or Dandy-Walker variant before 21 weeks' gestational age, compared to 14 fetuses with a diagnosis of Dandy-Walker malformation or variant between 21 weeks' gestation and delivery. A total of 24 fetuses had Dandy-Walker malformation and four had Dandy-Walker variant. Eight of the fetuses with the malformation had ventriculomegaly: one of the fetuses with early diagnosis and seven with later diagnosis (p = 0.027). None of the fetuses with Dandy-Walker variant had ventriculomegaly. The overall prevalence of concomitant structural abnormalities was 13/28; 8/14 for fetuses with early prenatal diagnosis and 5/14 for fetuses with late prenatal diagnosis of the malformation or the variant. Chromosomal abnormality rates were significantly higher among fetuses with early prenatal diagnosis (7/14) than among those with later prenatal diagnosis (1/14; p = 0.032). Abnormal karyotypes were more prevalent among fetuses without ventriculomegaly (7/20), compared to fetuses with ventriculomegaly (1/8). We conclude that fetuses with an antenatal diagnosis of Dandy-Walker malformation or Dandy-Walker variant before 21 weeks' gestational age have worse prognosis than fetuses with a later prenatal diagnosis of the same defect.
本研究调查了14例在孕21周前被诊断为Dandy-Walker畸形或Dandy-Walker变异型的胎儿以及14例在孕21周至分娩期间被诊断为Dandy-Walker畸形或变异型的胎儿中合并结构和染色体异常的发生率。共有24例胎儿患有Dandy-Walker畸形,4例患有Dandy-Walker变异型。患有畸形的胎儿中有8例出现脑室扩大:早期诊断的胎儿中有1例,晚期诊断的胎儿中有7例(p = 0.027)。患有Dandy-Walker变异型的胎儿均未出现脑室扩大。合并结构异常的总体发生率为13/28;畸形或变异型胎儿早期产前诊断的为8/14,晚期产前诊断的为5/14。早期产前诊断的胎儿染色体异常率(7/14)显著高于晚期产前诊断的胎儿(1/14;p = 0.032)。与有脑室扩大的胎儿(1/8)相比,无脑室扩大的胎儿(7/20)中异常核型更为普遍。我们得出结论,孕21周前产前诊断为Dandy-Walker畸形或Dandy-Walker变异型的胎儿预后比同一缺陷的晚期产前诊断胎儿更差。