摘要
目的：探讨小儿先天性巨细胞包涵体病的影像诊断问题。材料与方法：对１０年间所确诊的９例患儿头部ＣＴ资料及临床资料进行了回顾性分析。结果：脑室系统扩张、室周脑质不规则低密度变、脑室边缘散在斑点状钙化及小头畸形等较具特征。结论：ＣＴ所见加之新生儿期溶血性黄疸、肝脾肿大和发育期的运动、智力及行为异常等有助于诊断本病。
Purpose:Toinvestigatetheimagingdiagnosisofcytomegalicinclusiondiseaseinchil-dren.Materialsandmethods:CTmanifestationsandclinicaldataof9patientswithcongenitalgiantcelinclusiondiseaseduringtenyearswereanalysedretrospectively.Results:Ventriculardilatation,periventricularirregularlow-densityareas,periventricularpatchycalcificationsandmicrocephalywerethemainCTfindings.Conclusion:Inneonatalperiod,hemolyticjaundiceandhep-atosplenomegalyandingrowthstage,motormentalandbehaviordisordersincombinationwiththeCTfeaturesmaybehelpfultothediagnosis.
出处
《中华放射学杂志》
CAS
CSCD
北大核心
1996年第10期669-671,共3页
Chinese Journal of Radiology
关键词
神经系统疾病
巨细胞包涵体病
儿童
CT
诊断
NervoussystemdiseasesCytomegalicinclusiondiseaseTomography,X-raycomputed
