Jay V, Becker L E, Otsubo H, Hwang P A, Hoffman H J, Harwood-Nash D
Department of Pathology, Hospital for Sick Children/Bloorview Epilepsy Program, University of Toronto, Ontario, Canada.
J Neurosurg. 1993 Jul;79(1):53-61. doi: 10.3171/jns.1993.79.1.0053.
Significant pathological abnormalities were encountered in a series of 20 temporal lobectomies in children with intractable complex partial seizures. In particular, "dual pathology" (mesial temporal sclerosis with other lesions) was found rather than mesial temporal sclerosis as the only lesion. Unusual pathological findings included capillary penetration of neurons in a neuronal heterotopia in one patient, and foci of extensive cortical disorganization in some cases of mixed tumors and gangliogliomas. A high proportion of neuronal migration disorders was also seen with overlapping pathological features between cortical dysplasia and tuberous sclerosis. In this correlative clinical, radiological, electroencephalographic, and pathological study, some of the pathological lesions in children did not fit the classical categories of neoplasia and malformation and transitional forms were rarely encountered.
在一系列针对患有顽固性复杂部分性癫痫的儿童进行的20例颞叶切除术中,发现了显著的病理异常。特别是,发现的是“双重病理”(内侧颞叶硬化合并其他病变),而不是仅以内侧颞叶硬化作为唯一病变。不寻常的病理发现包括1例患者神经元异位症中神经元的毛细血管侵入,以及在一些混合性肿瘤和神经节胶质瘤病例中广泛的皮质结构紊乱灶。还发现高比例的神经元迁移障碍,其在皮质发育异常和结节性硬化症之间具有重叠的病理特征。在这项相关的临床、放射学、脑电图和病理学研究中,儿童的一些病理病变不符合肿瘤形成和畸形的经典类别,并且很少遇到过渡形式。