Su M, Wakabayashi K, Tanno Y, Inuzuka T, Takahashi H
Department of Pathology, Niigata University, Japan.
No To Shinkei. 1996 Oct;48(10):931-6.
We report a 72-year-old man with sporadic amyotrophic lateral sclerosis (ALS) who showed concomitant histopathology of Alzheimer's disease (AD) and incidental Lewy body disease. The patient presented at the age of 70 years with distal upper limb amyotrophy. Thereafter, gait disturbance and respiratory distress progressed. Neuropathological examination showed mild frontal lobe and anterior spinal root atrophy. There was moderate loss of upper and lower motor neurons, and Bunina bodies and skein-like inclusions were present in the spinal anterior horns and facial and hypoglossal nuclei, confirming the pathology of ALS. In addition, however, numerous amyloid plaques were observed throughout the entire cerebral neocortex, nucleus accumbens and amygdaloid body. Many neurofibrillary tangles were also evident in the medial temporal cortex. Moreover, the substantia nigra showed mild degeneration, and Lewy bodies were found in the substantia nigra, locus ceruleus, basal nucleus of Meynert and peripheral autonomic ganglia. Although neither parkinsonism nor dementia was noted during the clinical course, our final neuropathological diagnosis was sporadic ALS, AD and incidental Lewy body disease (or presymptomatic Parkinson's disease). Whether or not the coexistence of these three diseases in the same patient was merely coincidental is of considerable interest.
我们报告了一名72岁患有散发性肌萎缩侧索硬化症(ALS)的男性患者,其同时表现出阿尔茨海默病(AD)的组织病理学特征以及偶发性路易体病。该患者70岁时出现上肢远端肌萎缩。此后,步态障碍和呼吸窘迫逐渐加重。神经病理学检查显示轻度额叶和前脊髓根萎缩。上下运动神经元有中度丧失,脊髓前角以及面神经核和舌下神经核中存在布尼亚小体和丝状包涵体,证实了ALS的病理特征。然而,此外在整个大脑新皮层、伏隔核和杏仁体中观察到大量淀粉样斑块。内侧颞叶皮层中也可见许多神经原纤维缠结。此外,黑质显示轻度变性,在黑质、蓝斑、迈内特基底核和外周自主神经节中发现路易体。尽管在临床过程中未观察到帕金森综合征或痴呆,但我们最终的神经病理学诊断为散发性ALS、AD和偶发性路易体病(或症状前帕金森病)。同一患者中这三种疾病的共存是否仅仅是巧合,这一问题相当引人关注。