Division of Pediatric Neurology, Departments of Pediatrics and Neurology, The University of Utah School of Medicine, Salt Lake City, Utah.
Department of Medical Imaging, Primary Children's Hospital, Salt Lake City, Utah; Department of Radiology, The University of Utah, Salt Lake City, Utah.
Pediatr Neurol. 2014 Mar;50(3):218-23. doi: 10.1016/j.pediatrneurol.2013.11.005. Epub 2013 Nov 16.
Human cytomegalovirus, a major cause of permanent neurodevelopmental disability in children, frequently produces intracranial abnormalities, including calcifications and polymicrogyria, in infants with congenital cytomegalovirus infections. This report describes the features of cerebral cortical clefting, including schizencephaly, in children with congenital cytomegalovirus infection.
This is a retrospective review of the medical records of infants and children with congenital cytomegalovirus infection evaluated at Primary Children's Medical Center, Salt Lake City, Utah, between 1999 and 2008.
Twenty-five children with congenital cytomegalovirus infection were identified during this 10-year period; 23 (92%) had computed tomography and 17 (68%) had magnetic resonance imaging. Imaging was obtained at a median age of 6 months (mode 1 month or less). Of 15 children with confirmed congenital infections, 10 (66%) had polymicrogyria or abnormal gyral patterns, five (33%) had cleft cortical dysplasia, and two (13%) had schizencephaly. Of 10 children with suspected congenital cytomegalovirus infection, eight (80%) had polymicrogyria, two (20%) had cleft cortical dysplasia, and one (10%) had bilateral schizencephaly with calcifications. Seventeen of the 25 infants (68%) had intracranial calcifications.
These results indicate that clefting, either as cleft cortical dysplasia or schizencephaly, is an important feature of congenital cytomegalovirus infection.
人巨细胞病毒是导致儿童永久性神经发育障碍的主要原因,常导致先天性巨细胞病毒感染婴儿出现颅内异常,包括钙化和多微小脑回。本报告描述了先天性巨细胞病毒感染患儿脑皮质裂的特征,包括脑裂畸形。
这是对犹他州盐湖城初级儿童医疗中心 1999 年至 2008 年间评估的先天性巨细胞病毒感染婴儿和儿童的病历进行的回顾性分析。
在这 10 年期间,共发现 25 例先天性巨细胞病毒感染患儿;23 例(92%)行计算机断层扫描,17 例(68%)行磁共振成像。影像学检查中位数年龄为 6 个月(模式为 1 个月或以下)。在 15 例确诊的先天性感染患儿中,10 例(66%)有多微小脑回或异常脑回模式,5 例(33%)有皮质裂畸形,2 例(13%)有脑裂畸形。在 10 例疑似先天性巨细胞病毒感染的患儿中,8 例(80%)有多微小脑回,2 例(20%)有皮质裂畸形,1 例(10%)有双侧脑裂畸形伴钙化。25 例婴儿中有 17 例(68%)有颅内钙化。
这些结果表明,裂脑畸形,无论是皮质裂畸形还是脑裂畸形,都是先天性巨细胞病毒感染的一个重要特征。