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胼胝体异常:与脑部其他异常的相关性。

Anomalies of the corpus callosum: correlation with further anomalies of the brain.

作者信息

Barkovich A J, Norman D

机构信息

Department of Radiology, Letterman Army Medical Center, Presidio of San Francisco, CA 94129-6700.

出版信息

AJR Am J Roentgenol. 1988 Jul;151(1):171-9. doi: 10.2214/ajr.151.1.171.

DOI:10.2214/ajr.151.1.171
PMID:3259802
Abstract

The MR imaging studies of 68 patients who had brain anomalies were reviewed retrospectively to evaluate specific anatomic abnormalities of the corpus callosum. The corpus callosum was abnormal in 32 (47%) of the 68 patients. Excluding patients with the Chiari I malformation, callosal anomalies were present in 30 (68%) of 44 patients. Callosal dysgenesis was most common, followed by callosal atrophy or hypoplasia and complete agenesis. The anterior commissure was present in all patients. On the basis of the known temporal sequence of brain and callosal embryogenesis, we deduced the following regarding the pathogenesis of developmental anomalies: (1) callosal dysgenesis occurs as a result of insults during the formation of its precursors, not during formation of the corpus callosum itself; (2) the Dandy-Walker malformation sometimes occurs as a result of an insult in the eighth week of gestation, several weeks later than has been generally accepted; (3) sphenoidal encephaloceles probably occur as a result of faulty disjunction of neuroectoderm and cutaneous ectoderm at the anterior neuropore; and (4) a complete but atrophic corpus callosum results from an insult to the cortex or white matter after formation of the corpus callosum is complete (18-20 weeks). Callosal anomalies, easily identified on MR, are an important indicator of additional brain anomalies. Analysis of the corpus callosum provides important information about the embryogenesis of brain anomalies and may assist in distinguishing between in utero and perinatal brain insults.

摘要

回顾性分析68例脑异常患者的磁共振成像(MR)研究,以评估胼胝体的特定解剖异常。68例患者中32例(47%)胼胝体异常。排除Chiari I畸形患者后,44例患者中有30例(68%)存在胼胝体异常。胼胝体发育不全最为常见,其次是胼胝体萎缩或发育不全以及完全缺如。所有患者均存在前连合。根据已知的脑和胼胝体胚胎发育的时间顺序,我们对发育异常的发病机制推断如下:(1)胼胝体发育不全是由于其前体形成过程中受到损伤所致,而非胼胝体本身形成过程中受到损伤;(2)Dandy-Walker畸形有时是由于妊娠第8周受到损伤所致,比普遍认为的时间晚几周;(3)蝶骨脑膨出可能是由于神经外胚层和皮肤外胚层在前神经孔处分离错误所致;(4)完整但萎缩的胼胝体是由于胼胝体完全形成(18 - 20周)后皮质或白质受到损伤所致。胼胝体异常在MR上易于识别,是其他脑异常的重要指标。对胼胝体的分析提供了有关脑异常胚胎发育的重要信息,并可能有助于区分宫内和围产期脑损伤。

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