Wolf H K, Birkholz T, Wellmer J, Blümcke I, Pietsch T, Wiestler O D
Department of Neuropathology, University of Bonn Medical Center, Germany.
J Neuropathol Exp Neurol. 1995 Sep;54(5):689-97. doi: 10.1097/00005072-199509000-00011.
Gangliogliomas, dysembryoplastic neuroepithelial tumors (DNT) and glioneuronal malformations are frequently encountered in patients with pharmacoresistant focal epilepsies. In order to characterize the neurochemical profile of these neoplastic and malformative glioneuronal lesions, we have examined the presence of the alpha 1 subunit of the GABAA receptor, the N-methyl-D-aspartate receptor subunit 1 (NR1), glutamate decarboxylase, tyrosine hydroxylase, somatostatin, parvalbumin, and calretinin in 60 gangliogliomas, 11 DNT, 10 tuberous sclerosis-like lesions and 17 non-tuberous sclerosis-like glioneuronal malformations. All DNT and tuberous sclerosis-like lesions, 59 gangliogliomas (98%), and 13 non-tuberous sclerosis-like hamartias (76%) were positive for at least one of the markers. Despite a great variation between and within the different entities, the neurochemical profile was generally reminiscent of normal neocortex: glutamate decarboxylase, GABAA receptor and NR1 which are common in neocortical neurons were present in the great majority of the lesions and often showed high labeling indices. There were three tuberous sclerosis-like lesions (30%) that contained both NR1 and glutamate decarboxylase immunoreactive giant cells in addition to well-differentiated ganglion cells. This supports the idea that at least some of these giant cells are of neuronal origin. The oligodendroglia-like cells of DNT and glioneuronal hamartias did not show immunoreactivity for any of the markers. The very high incidence of ganglioglial lesions in patients with chronic focal epilepsies and the presence of neurotransmitter-producing enzymes, neurotransmitter receptors, neuropeptides, and calcium-binding proteins in many of these lesions suggests that they may play an active role in the pathogenesis of epileptic seizures.
神经节胶质瘤、胚胎发育不良性神经上皮肿瘤(DNT)和神经胶质神经元畸形在药物难治性局灶性癫痫患者中很常见。为了描述这些肿瘤性和畸形性神经胶质神经元病变的神经化学特征,我们检测了60例神经节胶质瘤、11例DNT、10例结节性硬化样病变和17例非结节性硬化样神经胶质神经元畸形中γ-氨基丁酸A受体α1亚基、N-甲基-D-天冬氨酸受体亚基1(NR1)、谷氨酸脱羧酶、酪氨酸羟化酶、生长抑素、小白蛋白和钙视网膜蛋白的存在情况。所有DNT和结节性硬化样病变、59例神经节胶质瘤(98%)以及13例非结节性硬化样错构瘤(76%)至少对一种标志物呈阳性。尽管不同实体之间以及同一实体内存在很大差异,但神经化学特征总体上使人联想到正常新皮层:新皮层神经元中常见的谷氨酸脱羧酶、γ-氨基丁酸A受体和NR1在大多数病变中都存在,且通常显示出高标记指数。有3例结节性硬化样病变(30%)除了有分化良好的神经节细胞外,还含有NR1和谷氨酸脱羧酶免疫反应性巨细胞。这支持了至少其中一些巨细胞起源于神经元的观点。DNT和神经胶质神经元错构瘤的少突胶质细胞样细胞对任何标志物均无免疫反应性。慢性局灶性癫痫患者中神经节胶质瘤病变的发生率非常高,并且许多这些病变中存在产生神经递质的酶、神经递质受体、神经肽和钙结合蛋白,这表明它们可能在癫痫发作的发病机制中起积极作用。