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儿童神经元移行异常性脑回畸形的CT表现 被引量:2

CT Features of the Gyral Malformation of Neuronal Migrational Anomaly in Children
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摘要 目的:分析神经元移行异常所引起的脑回发育畸形的 CT表现。材料和方法:回顾性分析 20例神经元移行异常脑回畸形的CT表现。结果:20例中,无脑回畸形3例,非无脑回畸形17例。前者表现为普遍性脑皮质均匀增厚,无脑沟形成或仅有少而浅的脑沟,脑表面光滑,脑回宽而扁平。后者表现为非普遍性脑皮质不均匀增厚,增厚皮质边缘高低不平,呈小波浪状或结节状隆起,增厚的皮质向深部折迭,形成皮质裂,部分病例白质内见胶质增生。结论:CT能够鉴别无脑回畸形和非无脑回畸形,为外科治疗由此而引起的难治性癫痫手术方案的选择提供依据。 Purpose: To analyse CT manifestations of gyral malformations of neuronal migrationl anomaly. Materials and Methods: CT manifestations of 20 patients with gyral malformation of neuronal migrational anomaly were retrospectively reviewed. Results: of the 20 patients, the lissencephalic type presented in 3 cases; the nonlissencephalic type was seen in 17 cases. The former showed that the cortex was an excessively uniform thickened without sulci, and brain surface was smooth (agyria), or only with a few and shallow sulci, and gyri were broad and flat (pachygyria). The latter CT findings were as follows: 1. A nongeneralized thickened, irregularly, bumpy cortex showed a wave form or a nodual bulge. 2. A deep infolding of thickened cortex. Gliosis in the white matter were seen in the nonlissencephalic type. Conclusion: CT was capable of differentiating lissencephaly from nonlissencephalic conical dysplasia and could provide valuable information for selecting surgical treatment planning of refractory epilepsy arising form these lesions.
出处 《中国医学影像学杂志》 CSCD 2000年第3期193-195,共3页 Chinese Journal of Medical Imaging
关键词 神经元移行异常 CT 婴儿 儿童 诊断 neuronal migration anomaly CT
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参考文献4

  • 1[1]Barkovich AJ, Truwit CL. Disorder of brain development. In: atlas SW, ed. Magnetic resonance imaging of the brain and spine. Lippincott-Raven Philadelphiaa, 2nd ed, 1996, 240
  • 2[2]Bar kovich AJ, Kjos BO. Schizencephaly: correlation of clinical findings with MR characteristics. AJNR, 1992, 13:85
  • 3[3]Bar kovich AJ, Kjos BO. Nonlissencephalic cortical dysplasia: correlation of imaging findings with clinical deficits. AJNR, 1992, 13:95
  • 4[4]Barth PG: Schizencephaly and Nonlissencephalic cortical dysplasia. AJNR, 1992, 13:104

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