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140例婴儿痉挛症的病因分类:正电子发射断层扫描的作用

Etiologic classification of infantile spasms in 140 cases: role of positron emission tomography.

作者信息

Chugani H T, Conti J R

机构信息

Department of Pediatrics, Wayne State University School of Medicine, Detroit, MI, 48201, USA.

出版信息

J Child Neurol. 1996 Jan;11(1):44-8. doi: 10.1177/088307389601100111.

Abstract

The classification of infantile spasms into symptomatic, cryptogenic, and idiopathic subgroups depends on clinical examination and available diagnostic technology. Positron emission tomography (PET) of glucose utilization is a powerful tool in detecting brain malformations (particularly cortical dysplasia) in infants with spasms. We analyzed etiologic data from 140 such infants, 78 girls and 62 boys, ages 2 months to 4 years 10 months (mean, 17 months). All had been evaluated extensively in one of two major medical centers. It should be emphasized that our referral population is biased toward infants with intractable spasms who fail to show a structural lesion. Seven patients had neurocutaneous syndromes, two had chromosomal abnormalities, two had inborn errors of metabolism, and one each had craniosynostosis or Menkes syndrome. Computed tomography and/or magnetic resonance imaging detected lesions in another 29 infants (20.7%) who did not have a specific disease or syndrome. Without the benefit of PET, the total number of symptomatic cases was 42 (30.0%). One infant, classified as idiopathic, had normal development and PET. In 97 cryptogenic cases, PET uncovered unifocal abnormalities in 30 and multifocal abnormalities in 62. Diffuse PET abnormalities, which did not provide specific etiologic information, were seen in three infants. Another two infants had normal PET scans. Thus, with the benefit of PET, the number of symptomatic cases rose dramatically from 42 (30.0%) to 134 (95.7%). The majority of unifocal and multifocal abnormalities on PET are believed to represent dysplastic lesions.

摘要

婴儿痉挛症分为症状性、隐源性和特发性亚组,这取决于临床检查和现有的诊断技术。葡萄糖利用的正电子发射断层扫描(PET)是检测痉挛婴儿脑畸形(尤其是皮质发育异常)的有力工具。我们分析了140例此类婴儿的病因数据,其中78名女孩和62名男孩,年龄在2个月至4岁10个月之间(平均17个月)。所有患儿均在两个主要医疗中心之一进行了全面评估。应该强调的是,我们的转诊人群偏向于患有顽固性痉挛且未显示结构性病变的婴儿。7例患者患有神经皮肤综合征,2例有染色体异常,2例有先天性代谢缺陷,1例分别患有颅缝早闭或门克斯综合征。计算机断层扫描和/或磁共振成像在另外29名(20.7%)没有特定疾病或综合征的婴儿中检测到病变。在没有PET检查的情况下,症状性病例总数为42例(30.0%)。1名被归类为特发性的婴儿发育正常且PET检查正常。在97例隐源性病例中,PET发现30例为单灶性异常,62例为多灶性异常。3例婴儿出现弥漫性PET异常,但未提供具体病因信息。另外2例婴儿PET扫描正常。因此,借助PET检查,症状性病例数从42例(30.0%)大幅上升至134例(95.7%)。PET上的大多数单灶性和多灶性异常被认为代表发育异常病变。

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