Kinsler V A, Aylett S E, Coley S C, Chong W K, Atherton D J
Department of Dermatology, Great Ormond Street Hospital for Children NHS Trust, Great Ormond Street, London WC1N 3JH, UK.
Arch Dis Child. 2001 Feb;84(2):152-5. doi: 10.1136/adc.84.2.152.
To establish the prevalence of central nervous system (CNS) abnormalities on magnetic resonance imaging (MRI) in a population of children with congenital melanocytic naevi (CMN) over the head and/or spine, and to compare this with clinical findings.
Forty three patients identified from outpatient clinics underwent MRI of the brain and/or spine. These were reported by a paediatric radiologist and findings compared with the clinical picture.
Nine patients had abnormal clinical neurology, seven had abnormal findings on MRI, and six had both abnormal clinical and radiological findings. Only three of the abnormal MRIs showed features of intracranial melanosis. Three others showed structural brain abnormalities: one choroid plexus papilloma, one cerebellar astrocytoma, and one posterior fossa arachnoid cyst; the first two of these have not previously been described in association with CMN. The last abnormal MRI showed equivocal changes requiring reimaging.
The prevalence of radiological CNS abnormality in this group of children was 7/43. Six of these developed abnormal clinical neurological signs within the first 18 months of life, but two did not do so until after the MRI. Two of the CNS lesions were operable; for this reason we support the routine use of early MRI in this group.
确定头和/或脊柱患有先天性黑素细胞痣(CMN)的儿童群体中,磁共振成像(MRI)显示的中枢神经系统(CNS)异常的患病率,并将其与临床发现进行比较。
从门诊诊所确定的43例患者接受了脑部和/或脊柱的MRI检查。由儿科放射科医生进行报告,并将检查结果与临床表现进行比较。
9例患者临床神经学异常,7例MRI检查结果异常,6例临床和影像学检查结果均异常。仅3例异常MRI显示颅内黑素沉着症特征。另外3例显示脑部结构异常:1例脉络丛乳头状瘤、1例小脑星形细胞瘤和1例后颅窝蛛网膜囊肿;其中前两者此前未被描述与CMN相关。最后1例异常MRI显示变化不明确,需要再次成像。
该组儿童中放射学CNS异常的患病率为7/43。其中6例在出生后的前18个月内出现异常临床神经学体征,但2例直到MRI检查后才出现。2例CNS病变可进行手术;因此,我们支持对该组儿童常规使用早期MRI检查。