Nordborg C, Eriksson S, Rydenhag B, Uvebrant P, Malmgren K
Institute of Laboratory Medicine, Department of Pathology, Sahlgrenska University Hospital, Göteborg, Sweden.
J Neurol Neurosurg Psychiatry. 1999 Oct;67(4):521-4. doi: 10.1136/jnnp.67.4.521.
Malformations of cortical development are commonly associated with epilepsy. In the first 139 consecutive patients in the Göteborg epilepsy surgery series, parenchymal malformations were found in 56. 1% of the children and in 23.1% of the adults. Microdysgenesis (MDG), which was the most common parenchymal malformation, was found in 35. 1% of the children and in 16.7% of the adults. The aim of this study was to identify clinical characteristics of patients with MDG. Mental retardation was found to be significantly more common in patients with major parenchymal malformations and in patients with MDG compared with patients without parenchymal malformations. Patients with major parenchymal malformations as well as patients with MDG also had a significantly earlier onset of seizures than patients without parenchymal malformations, also when adjusting for mental retardation. Patients with MDG were in these clinical aspects shown to closely resemble patients with major malformations. These findings suggest that MDG is a pathoanatomical entity of clinical relevance, with implications both in mental retardation and in epileptogenesis.
皮质发育畸形通常与癫痫相关。在哥德堡癫痫手术系列的首批139例连续患者中,56.1%的儿童和23.1%的成人发现有实质畸形。微发育异常(MDG)是最常见的实质畸形,在35.1%的儿童和16.7%的成人中被发现。本研究的目的是确定MDG患者的临床特征。与无实质畸形的患者相比,发现主要实质畸形患者和MDG患者中智力迟钝明显更为常见。主要实质畸形患者以及MDG患者的癫痫发作起始时间也明显早于无实质畸形的患者,即使在调整智力迟钝因素后也是如此。在这些临床方面,MDG患者显示出与主要畸形患者非常相似。这些发现表明,MDG是一个具有临床相关性的病理解剖实体,对智力迟钝和癫痫发生都有影响。