Nishida Namiko, Hayase Yoneko, Mikuni Nobuhiro, Enatsu Rei, Hayashi Naoki, Takahashi Jun A, Nakashima Yasuaki, Ikeda Akio, Amano Shigeru, Hashimoto Nobuo
Department of Neurosurgery, Kyoto University Graduate School of Medicine, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.
Brain Tumor Pathol. 2005;22(1):35-40. doi: 10.1007/s10014-005-0176-3.
We report here an intractable epilepsy case with fairly typical clinicoradiological features of dysembryoplastic neuroepithelial tumor (DNT), which means onset of seizures at a young age accompanying a medial temporal cystic lesion enclosed in cortical dysplasia (CD). The medial cystic lesion was composed of two morphologically distinct components; one was oligo-like and the other showed some tendency toward neuronal and glial differentiation, even though they were morphologically different from a so-called specific glioneural element (SGE). Epileptiform discharges were detected not only on the medial lesion but also on the lateral inferior temporal gyrus, which was confirmed as CD. According to both histopathological and clinical features, we named the lesion a nonspecific form of DNT.
我们在此报告一例难治性癫痫病例,其具有胚胎发育不良性神经上皮肿瘤(DNT)相当典型的临床放射学特征,即发病年龄较轻,伴有皮质发育异常(CD)所包绕的颞叶内侧囊性病变。内侧囊性病变由两个形态学上不同的成分组成;一个类似少突胶质细胞,另一个虽在形态上不同于所谓的特异性神经胶质成分(SGE),但显示出一些向神经元和神经胶质分化的倾向。不仅在内侧病变处检测到癫痫样放电,在外侧颞下回(经证实为CD)也检测到了癫痫样放电。根据组织病理学和临床特征,我们将该病变命名为非特异性形式的DNT。