Barkovich A J, Chuang S H, Norman D
Department of Radiology, Letterman Army Medical Center, Presidio of San Francisco, CA 94129-6700.
AJR Am J Roentgenol. 1988 Jan;150(1):179-87. doi: 10.2214/ajr.150.1.179.
Migration anomalies are congenital malformations caused by insults to migrating neuroblasts during the third to fifth gestational months. Included in this group are agyria, pachygyria, polymicrogyria, unilateral megalencephaly, schizencephaly, and gray matter heterotopias. Patients who have these conditions present clinically with developmental delay and seizures, and abnormal motor skills are noted in the more severely affected infants. To determine the utility of MR as a method for imaging in these patients, we used MR to evaluate 13 patients who had the full spectrum of migration anomalies. MR was more sensitive than CT in detecting these anomalies because of its better contrast between gray and white matter. We found that MR was particularly more sensitive in detecting schizencephaly, where recognizing the presence of gray matter lining the cleft is critical to distinguishing that disease from porencephaly, and in detecting polymicrogyria, where critical details of cortical architecture are obscured on CT by the overlying bone. Multiplanar capabilities were also found to be essential, since narrow clefts may not be detected when the imaging plane is parallel to the cleft. MR should be the primary imaging method for infants who have seizures or developmental delay.
移行异常是在妊娠第三个月至第五个月期间,迁移中的神经母细胞受到损伤所导致的先天性畸形。这一组疾病包括无脑回畸形、巨脑回畸形、多小脑回畸形、单侧巨脑症、脑裂畸形和灰质异位症。患有这些疾病的患者临床上表现为发育迟缓、癫痫发作,在病情更严重的婴儿中可观察到异常的运动技能。为了确定磁共振成像(MR)作为这些患者成像方法的实用性,我们使用MR对13例患有各种移行异常的患者进行了评估。由于MR在灰质和白质之间具有更好的对比度,因此在检测这些异常方面比计算机断层扫描(CT)更敏感。我们发现,MR在检测脑裂畸形方面尤其敏感,识别裂隙内衬灰质的存在对于将该疾病与脑穿通畸形区分开来至关重要;在检测多小脑回畸形方面也更敏感,在CT上,皮质结构的关键细节会被上方的骨骼遮挡。多平面成像能力也被认为是必不可少的,因为当成像平面与裂隙平行时,可能无法检测到狭窄的裂隙。对于患有癫痫或发育迟缓的婴儿,MR应作为主要的成像方法。