Fetal Medicine and Surgery Unit, Giannina Gaslini Institute, Genoa, Italy.
Ultrasound Obstet Gynecol. 2013 Dec;42(6):687-90. doi: 10.1002/uog.12506.
To assess the presence and degree of indirect signs of agenesis of the corpus callosum (ACC) according to gestational age and determine the percentage of cases in which each sign is present by 24 gestational weeks.
We analyzed retrospectively 54 cases of ACC which underwent three-dimensional neurosonography at our unit between January 2005 and December 2012. A single examination was available in 48 cases and six cases were followed up longitudinally, giving a total of 69 examinations. The following variables were assessed: indication for referral, karyotype, width of the atrium and presence/absence of colpocephaly, the cavum septi pellucidi, dorsal cyst and additional central nervous system (CNS) and non-CNS anomalies.
Overall, there were 31 cases of complete ACC (cACC, 42 examinations) and 23 cases of partial ACC (pACC, 27 examinations). The mean gestational age was lower in the cases referred because of anomalies other than ACC than it was in those referred because of ventriculomegaly and/or suspicion of ACC (P < 0.05). Atrial width showed a positive linear correlation with advancing gestational age (P < 0.0001); it was < 10.0 mm in 25/34 (73.5%) examinations < 24 gestational weeks and in 9/35 (25.7%) ≥ 24 weeks (P < 0.001). Colpocephaly was present in 20.6% (7/34) of examinations < 24 weeks and in 68.6% (24/35) of those after 23 weeks (P < 0.05). The cavum septi pellucidi was present and visible at least in part in 17 (63%) of the 27 pACC examinations. In nine of the 27 (33.3%) pACC examinations, there was neither ventriculomegaly nor absence of the cavum septi pellucidi. Associated anomalies were present in 25/54 (46.3%) cases, and in 11 these included or consisted of CNS abnormalities. Karyotype was abnormal in seven of the 40 (17.5%) cases in which it was available.
In a significant proportion of cases, most of the indirect signs of ACC are either absent or barely visible at the time of the midtrimester screening ultrasound examination. Therefore, ACC may escape diagnosis at midtrimester screening ultrasound. In particular, a third of examinations in fetuses with pACC may not show any abnormality in the transventricular screening view < 24 weeks. The medicolegal implications of such findings are important and should be considered.
根据胎龄评估胼胝体发育不全(ACC)间接征象的存在和程度,并确定在 24 孕周时每种征象出现的病例百分比。
我们回顾性分析了 2005 年 1 月至 2012 年 12 月在我院行三维神经超声检查的 54 例 ACC 病例。48 例仅有单次检查,6 例为连续检查,共 69 次检查。评估的变量包括:转诊指征、核型、心房宽度和有无尖头畸形、透明隔腔、背侧囊肿及其他中枢神经系统(CNS)和非 CNS 异常。
共有 31 例完全性 ACC(cACC,42 次检查)和 23 例部分性 ACC(pACC,27 次检查)。由于 ACC 以外的异常而转诊的病例的平均胎龄低于因脑室扩大和/或怀疑 ACC 而转诊的病例(P<0.05)。心房宽度与胎龄呈正线性相关(P<0.0001);24 孕周前,25/34(73.5%)次检查<10.0mm,24 孕周后,9/35(25.7%)次检查≥10.0mm(P<0.001)。尖头畸形在 24 孕周前的 34 次检查中有 20.6%(7/34),在 24 孕周后的 35 次检查中有 68.6%(24/35)(P<0.05)。27 次 pACC 检查中有 17 次(63%)可见部分或全部透明隔腔。27 次 pACC 检查中有 9 次(33.3%)既无脑室扩大也无透明隔腔缺失。54 例中有 25 例(46.3%)存在合并畸形,其中 11 例包括 CNS 异常。在可进行核型分析的 40 例中,有 7 例(17.5%)异常。
在相当一部分病例中,ACC 的大多数间接征象在中孕期筛查超声检查时要么不存在,要么几乎看不见。因此,ACC 可能在中孕期筛查超声检查时漏诊。特别是,在 24 孕周前的 pACC 胎儿中,有三分之一的经脑室筛查视图可能没有任何异常。这些发现的医学法律意义很重要,应该考虑到。