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小儿21三体综合征的脑部CT表现
引用本文:吴义忠,陈犇,梁立华. 小儿21三体综合征的脑部CT表现[J]. 临床放射学杂志, 1999, 0(3): 174-175
作者姓名:吴义忠  陈犇  梁立华
作者单位:广东医学院附属医院放射科,广东医学院遗传教研室
摘    要:目的:地小和21三体综合征脑部CT表现的认识和诊断。材料与方法;回顾性分析23例经细胞遗传学检查证实的21三体综合征的脑部CT表现,结果:一病的CT特征为:(1)脑内钙化,多见于基底节区,呈点状或小圆形;(2)侧裂、额顶区蛛网膜下腔增宽;(3)小脑发育不全。结论:本病CT表现具有一定的特征性,但其CT诊断须结合细胞遗传学检查确定。

关 键 词:21三体综合征 CT 脑 先天愚型

Cerebral CT Manifestations of 21 Trisomy Syndrome in Children
Wu Yizhong,Chen Ben,Liang Lihua,et al.. Cerebral CT Manifestations of 21 Trisomy Syndrome in Children[J]. Journal of Clinical Radiology, 1999, 0(3): 174-175
Authors:Wu Yizhong  Chen Ben  Liang Lihua  et al.
Affiliation:Wu Yizhong,Chen Ben,Liang Lihua,et al. Department of Radiology,The Affiliated Hospital of Guangdong Medical College,Zhanjiang,Guangdong Province 524001,P.R.China
Abstract:Objective: To improve the understanding and diagnostic ability of the brain changes in 21 trisomy syndrome.Materials and Methods:Cerebral CT findings in 23 cases with 21 trisomy syndrome, proved by cytogenetics, were retrospectively analyzed.Results:CT findings were as follows: (1) spotty or small round calcifications, mainly seen in basal ganglia area; (2) dilated sylvian fissure and subarachnoid cavity in frontal and parietal lobes; (3) underdevelopment of cerebellum.Conclusion: Cerebral CT findings of 21 trisomy are characteristic, however, cytogenous examination should be conducted in order to confirm the diagnosis.
Keywords:trisomy syndrome Cerebral CT
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