Kusaka H, Imai T
Department of Neurology, Kitano Hospital, Osaka, Japan.
Clin Neuropathol. 1993 May-Jun;12(3):164-8.
One type of motor neuron disease (MND) associated with dementia is well known for the fact that it displays atrophy of the frontal and temporal lobes, neuronal loss and sponginess of the superficial layers of the cortex, and subcortical gliosis (so-called Mitsuyama type). In an attempt to determine characteristics of the pathology of motor neurons, three cases of MND with dementia were examined and compared with 16 cases of sporadic classical amyotrophic lateral sclerosis (ALS) with light and electron microscopes. All these cases with dementia showed loss of motor neurons, chromatolysis, spheroids, and Bunina bodies. Quantitative analyses of the 5th lumbar anterior horns showed no significant differences in incidences of chromatolysis and Bunina bodies between cases with and without dementia. Ultrastructures of the anterior horns were essentially identical in both groups. Therefore, the pathology of motor neurons at least in one type of MND with dementia seems to share common features with that in sporadic classical ALS without dementia.
一种与痴呆症相关的运动神经元疾病(MND)因以下特征而闻名:它表现为额叶和颞叶萎缩、神经元丧失以及皮质表层海绵样变和皮质下胶质增生(所谓的光山型)。为了确定运动神经元的病理学特征,对3例伴有痴呆症的MND患者进行了检查,并与16例散发性经典肌萎缩侧索硬化症(ALS)患者进行了光镜和电镜比较。所有这些伴有痴呆症的病例均显示运动神经元丧失、染色质溶解、球状体和布尼纳小体。对第5腰椎前角的定量分析表明,有痴呆症和无痴呆症的病例之间,染色质溶解和布尼纳小体的发生率无显著差异。两组前角的超微结构基本相同。因此,至少在一种伴有痴呆症的MND中,运动神经元的病理学似乎与无痴呆症的散发性经典ALS具有共同特征。