DELTA-Ultrasound Diagnosis Center in Obstetrics and Gynecology, Madrid, Spain.
FETALMED-Maternal-Fetal Diagnostic Center, Fetal Imaging Unit, Santiago, Chile.
Ultrasound Obstet Gynecol. 2018 Feb;51(2):199-207. doi: 10.1002/uog.17445. Epub 2018 Jan 2.
To assess non-visualization of the choroid plexus of the fourth ventricle (CP-4V) as a simple, qualitative and reproducible first-trimester ultrasound feature of the posterior fossa for the prediction of central nervous system (CNS) anomalies and chromosomal defects.
First-trimester three-dimensional ultrasound datasets of the fetal brain were obtained prospectively from 65 consecutive normal singletons and retrospectively from 27 fetuses identified as having an abnormal posterior fossa on first-trimester ultrasound examination, and randomly combined to form the final study group. The stored ultrasound volumes were analyzed offline by two accredited sonologists, who were not aware of the final diagnoses. The CP-4V was assessed by multiplanar navigation and classified as visible or non-visible in its normal position depending on whether or not the echogenic structure that separates the fourth ventricle from the cisterna magna was identified in both midsagittal and axial planes. Correlation with subsequent second-trimester ultrasound, fetal magnetic resonance imaging, or postmortem or postnatal findings was performed to determine the predictive value of the first-trimester findings.
Among the 92 ultrasound datasets analyzed, 73 (79%) were acquired transabdominally and 19 (21%) transvaginally. The CP-4V was classified as visible in 64 cases and non-visible in 28 cases, with agreement between the two observers in both sagittal and axial planes in all but one case. Twelve of the 28 (43%) fetuses with non-visible CP-4V were subsequently diagnosed as having a CNS malformation (open spina bifida (n = 6), Dandy-Walker malformation (n = 2), Blake's pouch cyst (n = 2), cephalocele (n = 1) and megacisterna magna (n = 1)). In addition, 20 of these 28 (71%) fetuses had aneuploidy (trisomy 18 (n = 10), triploidy (n = 5), trisomy 13 (n = 3), Turner syndrome (n = 1) or trisomy 21 (n = 1)). There was only one false-positive case, in which the CP-4V was classified as absent in a normal fetus.
Non-visualization of the CP-4V in the first trimester appears to be a strong marker of posterior fossa anomalies and chromosomal defects. Qualitative evaluation of this anatomic structure is simple, feasible and reproducible, and its routine assessment during the first-trimester scan may facilitate the early detection of CNS anomalies and associated fetal aneuploidy. Copyright © 2017 ISUOG. Published by John Wiley & Sons Ltd.
评估第四脑室脉络丛(CP-4V)的不可见性作为一种简单、定性和可重复的初孕期后颅窝超声特征,用于预测中枢神经系统(CNS)异常和染色体缺陷。
前瞻性地从 65 例连续的正常单胎中获得胎儿脑的初孕期三维超声数据集,并从 27 例在初孕期超声检查中发现后颅窝异常的胎儿中回顾性地获得,随机组合形成最终的研究组。由两名认可的超声医师离线分析存储的超声容积,他们不知道最终的诊断。通过多平面导航评估 CP-4V,并根据在正中矢状面和轴向平面是否识别出将第四脑室与脑池分开的回声结构,将其在正常位置分类为可见或不可见。与随后的中孕期超声、胎儿磁共振成像或尸检或产后结果相关联,以确定初孕期发现的预测价值。
在分析的 92 个超声数据集,73 例(79%)经腹部采集,19 例(21%)经阴道采集。CP-4V 在 64 例中分类为可见,在 28 例中分类为不可见,除 1 例外,两名观察者在所有矢状面和轴向平面的意见均一致。28 例不可见 CP-4V 的胎儿中,有 12 例(43%)随后诊断为 CNS 畸形(开放性脊柱裂(n=6),Dandy-Walker 畸形(n=2),Blake 袋囊肿(n=2),颅后窝脑膜膨出(n=1)和巨脑池(n=1))。此外,这 28 例中有 20 例(71%)胎儿存在非整倍体(18 三体(n=10),三倍体(n=5),13 三体(n=3),特纳综合征(n=1)或 21 三体(n=1))。只有 1 例假阳性病例,在正常胎儿中 CP-4V 被分类为不存在。
初孕期 CP-4V 不可见似乎是后颅窝异常和染色体缺陷的一个强有力的标志物。对这种解剖结构的定性评估简单、可行且可重复,在初孕期扫描中常规评估可有助于早期发现 CNS 异常和相关的胎儿非整倍体。