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部分性癫痫患者海马体的发育变化:磁共振成像与临床情况

Hippocampal developmental changes in patients with partial epilepsy: magnetic resonance imaging and clinical aspects.

作者信息

Baulac M, De Grissac N, Hasboun D, Oppenheim C, Adam C, Arzimanoglou A, Semah F, Lehéricy S, Clémenceau S, Berger B

机构信息

Clinique P. Castaigne, Höpital de la Pitié-Salpêtrière, Paris, France.

出版信息

Ann Neurol. 1998 Aug;44(2):223-33. doi: 10.1002/ana.410440213.

Abstract

Developmental disorders of the hippocampal formation (HF) have been described in epileptic syndromes associated with lissencephaly, but HF malformations can be found without widespread cortical changes. We report 19 patients with partial epilepsy and abnormal HF patterns on magnetic resonance imaging (MRI). The changes consisted of incomplete folding with abnormal medial location along the choroid fissure, globular shape and/or verticalization, and were observed in the following three contexts: (1) diffuse disorder of neuronal migration (n=1); (2) temporal lobe malformation (n=5), including heterotopia, abnormal gyration, and, in 2 cases, reduced HF volume; and (3) apparently isolated HF changes (n=13, bilateral in 3 cases). The clinical features were heterogeneous in terms of severity of epilepsy and, when the focus could be determined, in localization (temporal or extratemporal). In 4 patients with apparently isolated HF changes, MRI was suggestive of both abnormal development and hippocampal sclerosis. In these patients, presurgical investigation and postoperative results suggested multiple epileptogenic foci, involving the frontal lobes in 2 cases. One HF specimen was large enough for the observation of developmental abnormalities corresponding to the changes seen on MRI. HF changes in shape and/or position should be included among the structural abnormalities associated with partial epilepsies. They may represent the visible part of a more extensive or more distant disorder of brain development.

摘要

海马结构(HF)发育障碍已在与无脑回畸形相关的癫痫综合征中有所描述,但在无广泛皮质改变的情况下也可发现HF畸形。我们报告了19例部分性癫痫患者,其磁共振成像(MRI)显示HF模式异常。这些改变包括沿脉络膜裂的内侧位置异常、球状形态和/或垂直化的不完全折叠,且在以下三种情况下观察到:(1)神经元迁移的弥漫性障碍(n = 1);(2)颞叶畸形(n = 5),包括异位、异常脑回,2例中HF体积减小;(3)明显孤立的HF改变(n = 13,3例为双侧)。临床特征在癫痫严重程度方面以及在能够确定病灶时的定位(颞叶或颞外)方面存在异质性。在4例明显孤立的HF改变患者中,MRI提示发育异常和海马硬化。在这些患者中,术前检查和术后结果提示存在多个致痫灶,2例累及额叶。1个HF标本足够大,可观察到与MRI所见改变相对应的发育异常。HF的形态和/或位置改变应纳入与部分性癫痫相关的结构异常之中。它们可能代表更广泛或更远处脑发育障碍的可见部分。

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