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[端脑连合发育不全与发育异常(胼胝体发育不全及相关异常)的解剖学磁共振成像研究。临床关联与形态发生学解读]

[Anatomic MRI study of commissural agenesis and dysplasia of the Telencephalon (Agenesis of the corpus callosum and related anomalies). Clinical correlations and morphogenetic interpretation].

作者信息

Raybaud C, Girard N

出版信息

Neurochirurgie. 1998 May;44(1 Suppl):38-60.

PMID:9757324
Abstract

A series of 78 patients presenting with agenesis of the cerebral commissures and properly investigated with MR imaging, was reviewed and analyzed morphologically. Results were compared with descriptive data from the literature, and with the developmental models proposed. From this, a model of a-commissural brain is described: the lamina terminalis would be homologous to a telencephalic anterior medullary velum of which the commissure would be the anterior commissure, and the lamina of white matter described as the Probst's and the fornical bundles, would be homologous to a posterior medullary velum having become a medial medullary velum due to the division of the prosecephalon into two cerebral hemispheres, and of which the commissure would be the (posterior) calloso-hippocampal commissure. Also, the comparison with the model establishes that in the actual malformations, defects of the cingulum and of at least some of the intralobaroccipital association bundles are observed beside the commissural defect. Such a model would reclassify these disorders, distinguishing the "simple" commissural defects, complete or segmental, global or dissociated, without or with a ventricular expansion, from more complex forms with multicystic defects, adding major dysplastic lesions of the dura mater, leptomeninges and parenchyma, to the commissural defects. Paradoxically, the latter group seems to be clinically less severe than the "simple agenesis" group, of which prognosis (including the neurologic and intellectual disorders as well as the associated pathologies) is generally very poor; this should be seriously considered since the antenatal diagnosis of these malformations is made routinely with ultrasonography and MRI.

摘要

对78例表现为大脑连合缺如且接受了恰当磁共振成像检查的患者进行了回顾,并进行了形态学分析。将结果与文献中的描述性数据以及所提出的发育模型进行了比较。据此,描述了一种无连合脑模型:终板与端脑的前髓帆同源,其连合为前连合,被描述为普罗布斯特束和穹窿束的白质层与后髓帆同源,后髓帆因前脑分裂为两个大脑半球而变成内侧髓帆,其连合为(后)胼胝体 - 海马连合。此外,与该模型的比较表明,在实际畸形中,除了连合缺陷外,还观察到扣带和至少一些脑叶内枕叶联合束的缺陷。这样一个模型将对这些疾病进行重新分类,区分“简单”的连合缺陷,包括完全或节段性、整体或分离性、有无脑室扩张的情况,与更复杂的具有多囊性缺陷的形式,后者在连合缺陷的基础上增加了硬脑膜、软脑膜和实质的主要发育异常病变。矛盾的是,后一组在临床上似乎比“单纯发育不全”组症状轻,而“单纯发育不全”组的预后(包括神经和智力障碍以及相关病理情况)通常非常差;鉴于这些畸形通常通过超声和磁共振成像进行产前诊断,这一点应予以认真考虑。

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