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婴儿痉挛症患儿的后颅窝异常

Posterior fossa abnormalities in children with infantile spasms.

作者信息

Schiffmann R, Mannheim G B, Stafstrom C E, Hamburger S D, Holmes G L

机构信息

Pediatric Neurology Unit, Hadassah University Hospital, Jerusalem, Israel.

出版信息

J Child Neurol. 1993 Oct;8(4):360-5. doi: 10.1177/088307389300800413.

Abstract

In order to explore possible pathophysiologic involvement of the brain stem in infantile spasms, we retrospectively compared clinical and electroencephalographic (EEG) features of 14 children with infantile spasms who had gross posterior fossa abnormalities on neuroimaging studies with 84 children with infantile spasms who had either normal neuroimaging (n = 19) or supratentorial abnormalities (n = 65). Children with posterior fossa abnormalities how lower mean initial and follow-up developmental quotients compared to those with normal imaging or supratentorial abnormalities alone. Age of onset of infantile spasms, latency to treatment, response to steroids, and follow-up EEG pattern were not significantly different among the three groups. Six children (6%) had Dandy-Walker cysts, an association rarely reported with infantile spasms. We conclude that the presence of posterior fossa abnormalities in patients with infantile spasms portends a relatively poor developmental outcome.

摘要

为了探究脑干在婴儿痉挛症中可能的病理生理参与情况,我们回顾性比较了14例在神经影像学检查中发现后颅窝明显异常的婴儿痉挛症患儿与84例神经影像学正常(n = 19)或幕上异常(n = 65)的婴儿痉挛症患儿的临床和脑电图(EEG)特征。与单纯影像学正常或幕上异常的患儿相比,后颅窝异常的患儿平均初始和随访发育商较低。三组患儿在婴儿痉挛症的发病年龄、治疗延迟时间、对类固醇的反应以及随访脑电图模式方面无显著差异。6例患儿(6%)患有Dandy-Walker囊肿,这一关联在婴儿痉挛症中鲜有报道。我们得出结论,婴儿痉挛症患者存在后颅窝异常预示着发育结局相对较差。

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