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胼胝体区域伴有脂肪瘤的中线发育异常。

Midline developmental anomalies with lipomas in the corpus callosum region.

作者信息

Kieslich M, Ehlers S, Bollinger M, Jacobi G

机构信息

Department of Pediatric Neurology, Johann Wolfgang Goethe-University, Frankfurt/Main, Germany.

出版信息

J Child Neurol. 2000 Feb;15(2):85-9. doi: 10.1177/088307380001500205.

Abstract

Three children with complete or partial callosal aplasia and intracranial lipoma in the corpus callosum region were investigated. Two lipomas were tubulonodular; one replaced the entire corpus callosum structure. Accompanying anomalies affected the cingulate gyrus, septum pellucidum, and choroid plexus. In one case, diagnosis was made in utero in the 25th gestational week by ultrasonography; in the second case it was made on the first day of life, also by screening ultrasonography. Two children had mild spastic distal diparesis; one complained of chronic headache. Electroencephalography showed no abnormalities; epilepsy anamnesis was negative. Somatosensory and visual evoked potentials showed prolonged conduction in two cases. Surgery was not indicated. Because of the risk of developing epileptic seizures, regular electroencephalographic follow-up investigations are essential.

摘要

对3例胼胝体完全或部分发育不全且胼胝体区域存在颅内脂肪瘤的儿童进行了研究。2例脂肪瘤呈管状结节状;1例替代了整个胼胝体结构。伴随的异常影响扣带回、透明隔和脉络丛。1例在孕25周时通过超声在子宫内确诊;第2例也是在出生第一天通过筛查超声确诊。2例儿童有轻度痉挛性远端双瘫;1例主诉慢性头痛。脑电图显示无异常;癫痫病史为阴性。体感诱发电位和视觉诱发电位在2例中显示传导延长。未建议手术。由于有发生癫痫发作的风险,定期进行脑电图随访检查至关重要。

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