Kidokoro Hiroyuki, Shiraki Anna, Torii Yuka, Tanaka Masaharu, Yamamoto Hiroyuki, Kurahashi Hirokazu, Maruyama Koichi, Okumura Akihisa, Natsume Jun, Ito Yoshinori
Department of Pediatrics, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8560, Japan.
Department of Pediatrics, Aichi Medical University, Nagakute, Japan.
Neuroradiology. 2021 May;63(5):761-768. doi: 10.1007/s00234-020-02603-9. Epub 2020 Nov 17.
Brain MRI provides important information about suspected congenital CMV infection in neonatally underdiagnosed children. This study aimed to describe MRI findings in children in whom congenital CMV infection was not suspected during the neonatal period and was proven retrospectively.
We enrolled 31 children referred to the pediatric neurology clinic with neurological symptoms who were proven to have congenital CMV infection based on dried umbilical cord samples. Upon diagnosis, MR and CT images were assessed using the van der Knaap scoring system integrated with additional variables. Two investigators independently assessed all images.
The age at diagnosis was < 12 months in 14, 12-24 months in 11, and > 24 months in 6 patients. The initial symptom triggering clinic referral was delayed development in 22, seizure in 5, deafness in 3, and hemiplegia in 1 patient. Of the 31 children, 30 had a white matter (WM) abnormality predominant in the deep WM of the parietal lobe (n = 25). Anterior temporal lesions were observed in 21 children. Cortical lesions were observed in 7 children, suggestive of polymicrogyria. No child had cerebellar or brainstem abnormalities. Brain CT was performed in 22 of 31 children, and 11 showed punctate cerebral calcification in the periventricular and/or deep WM.
Patients with congenital CMV infection with delayed neurological symptoms show a relatively uniform pattern of parietal-dominant multifocal WM lesions and anterior temporal lesions, with or without polymicrogyria.
脑部磁共振成像(MRI)可为新生儿期诊断不足的疑似先天性巨细胞病毒(CMV)感染儿童提供重要信息。本研究旨在描述在新生儿期未怀疑有先天性CMV感染且经回顾性证实的儿童的MRI表现。
我们纳入了31名因神经症状转诊至儿科神经科门诊的儿童,这些儿童基于干燥脐带样本被证实患有先天性CMV感染。诊断后,使用结合了其他变量的范德克纳普评分系统对磁共振成像(MR)和计算机断层扫描(CT)图像进行评估。两名研究人员独立评估所有图像。
诊断时年龄小于12个月的有14例,12至24个月的有11例,大于24个月的有6例。引发门诊转诊的初始症状为发育迟缓22例、癫痫发作5例、耳聋3例、偏瘫1例。在这31名儿童中,30例有白质(WM)异常,以顶叶深部白质为主(25例)。21名儿童观察到颞叶前部病变。7名儿童观察到皮质病变,提示多小脑回。没有儿童有小脑或脑干异常。31名儿童中有22名进行了脑部CT检查,11名在脑室周围和/或深部白质有斑点状脑钙化。
有延迟神经症状的先天性CMV感染患者表现出以顶叶为主的多灶性白质病变和颞叶前部病变的相对一致模式,有或没有多小脑回。