Chugani H T, Rintahaka P J, Shewmon D A
Department of Pediatrics, Children's Hospital of Michigan, Wayne State University, Detroit 48201.
Epilepsia. 1994 Jul-Aug;35(4):813-22. doi: 10.1111/j.1528-1157.1994.tb02517.x.
To determine seizure propagation patterns, we analyzed ictal positron emission tomography (PET) studies of regional cerebral glucose utilization in 18 children (11 male and 7 female aged 2 weeks to 16 years) with epilepsy (excluding infantile spasms IS). Three major metabolic patterns were determined based on degree and type of subcortical involvement: Nine children had type I; asymmetric glucose metabolism of striatum and thalamus. Of these, the 7 oldest children showed unilateral cortical hypermetabolism (always including frontal cortex) and crossed cerebellar hypermetabolism. Two infants (aged < 1 year) had a similar ictal PET pattern but no cerebellar asymmetry, presumably owing to immaturity of corticopontocerebellar projections. Five children had type II, symmetric metabolic abnormalities of striatum and thalamus; this pattern was accompanied by hippocampal or insular cortex hypermetabolism, diffuse neocortical hypometabolism, and absence of any cerebellar abnormality. Four children had type III, hypermetabolism restricted to cerebral cortex. This classification can accommodate ictal PET and single photon emission computed tomography (SPECT) patterns described by other investigators. Future studies should be directed at the clinical relevance of this classification, particularly with regard to epilepsy surgery.
为了确定癫痫发作的传播模式,我们分析了18例癫痫患儿(11例男性,7例女性,年龄2周至16岁,不包括婴儿痉挛症)的发作期正电子发射断层扫描(PET)研究,以观察局部脑葡萄糖利用情况。根据皮质下受累的程度和类型确定了三种主要代谢模式:9例患儿为I型,表现为纹状体和丘脑葡萄糖代谢不对称。其中,7名年龄较大的儿童表现为单侧皮质高代谢(总是包括额叶皮质)和交叉性小脑高代谢。2名婴儿(年龄<1岁)有类似的发作期PET模式,但无小脑不对称,可能是由于皮质桥脑小脑投射不成熟。5例患儿为II型,表现为纹状体和丘脑对称性代谢异常;这种模式伴有海马或岛叶皮质高代谢、弥漫性新皮质低代谢,且无任何小脑异常。4例患儿为III型,高代谢仅限于大脑皮质。这种分类能够涵盖其他研究者描述的发作期PET和单光子发射计算机断层扫描(SPECT)模式。未来的研究应针对这种分类的临床相关性,尤其是在癫痫手术方面。