Department of Maternal-Fetal Medicine, Hospital Universitari Vall d'Hebron, Universitat Autónoma de Barcelona, Barcelona, Spain.
Department of Obstetrics and Gynecology, Hospital Universitario La Paz, Madrid, Spain.
J Matern Fetal Neonatal Med. 2021 Feb;34(3):439-444. doi: 10.1080/14767058.2019.1609931. Epub 2019 Apr 29.
The main objective of this study was to evaluate the accuracy of prenatal ultrasound to diagnose corpus callosum alterations, compared to prenatal magnetic resonance imaging (MRI), postnatal image techniques (ultrasound and/or MRI), and post-mortem examination in terminated pregnancies. Retrospective review of 86 cases of prenatal ultrasound diagnosis of corpus callosum anomalies between January 2007 and December 2015 at a third level Maternal Fetal Medicine center. The study reviewed the findings of prenatal ultrasound and MRI, post-mortem examination in cases of termination of pregnancy (TOP) or stillbirths and postnatal ultrasound, and MRI in neonates. The anomalies of corpus callosum (CC) were classified as complete agenesis of the corpus callosum (ACC), partial ACC, or dysgenesis of CC. Fifty-eight (67.4%) cases resulted in TOP, 26 (30.2%) cases opted to continue with the pregnancy and two (2.3%) cases were lost to follow up. Among the 26 cases that continued with the pregnancy, 24 (92.3%) were live births and two (7.7%) were stillborn. All cases in which a third trimester MRI was performed ( = 46) confirmed the prenatal ultrasound diagnosis of CC anomaly. In seven (15.2%) of them, the MRI found additional intracranial findings and in three cases (6.5%) the type of CC anomaly (complete, partial, or dysgenesis) was reclassified (Kappa index: 0.86, 95% CI: 0.71-1.00). CC anomalies were confirmed in 46 (95.8%) of the 48 cases in which a post-mortem examination was available, the type of anomaly being reclassified in three cases (6.3%) (Kappa index: 0.88, 95% CI: 0.75-1.00). Among the 10 cases in which a postnatal ultrasound was performed, the CC anomaly was confirmed in all and the type of anomaly was reclassified in 1 (10%) of them (Kappa index: 0.75, 95% CI: 0.32-1.00). Corpus callosum agenesis can be detected on the routine mid-trimester ultrasound scan. Prenatal ultrasound and MRI can accurately classify the type of CC abnormality. Moreover, third trimester MRI can detect additional intracranial anomalies in 15% of cases.
本研究的主要目的是评估产前超声诊断胼胝体异常的准确性,与产前磁共振成像(MRI)、产后影像学技术(超声和/或 MRI)以及终止妊娠的尸检相比。回顾性分析 2007 年 1 月至 2015 年 12 月在三级母胎医学中心进行的 86 例产前超声诊断胼胝体异常的病例。研究回顾了产前超声和 MRI、终止妊娠(TOP)或死产的尸检、新生儿的超声和 MRI 的结果。胼胝体异常(CC)分为胼胝体完全缺如(ACC)、部分 ACC 或 CC 发育不良。58 例(67.4%)结果为 TOP,26 例(30.2%)选择继续妊娠,2 例(2.3%)失访。在继续妊娠的 26 例中,24 例(92.3%)为活产,2 例(7.7%)为死产。所有进行第三孕期 MRI 的病例(n=46)均证实了产前超声诊断的 CC 异常。其中 7 例(15.2%)MRI 发现了额外的颅内发现,3 例(6.5%)CC 异常的类型(完全、部分或发育不良)重新分类(Kappa 指数:0.86,95%CI:0.71-1.00)。48 例尸检可用的病例中,46 例(95.8%)证实存在 CC 异常,3 例(6.3%)重新分类异常类型(Kappa 指数:0.88,95%CI:0.75-1.00)。在 10 例进行了产后超声检查的病例中,所有病例均证实存在 CC 异常,其中 1 例(10%)重新分类异常类型(Kappa 指数:0.75,95%CI:0.32-1.00)。胼胝体缺如可在常规中孕期超声扫描中检出。产前超声和 MRI 可准确分类 CC 异常的类型。此外,第三孕期 MRI 可在 15%的病例中检测到额外的颅内异常。