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Sporadic motor neuron disease with Lewy body-like hyaline inclusions.

作者信息

Sasaki S, Yamane K, Sakuma H, Maruyama S

机构信息

Department of Neurology, Tokyo Women's Medical College, Japan.

出版信息

Acta Neuropathol. 1989;78(5):555-60. doi: 10.1007/BF00687719.

DOI:10.1007/BF00687719
PMID:2554635
Abstract

Lewy body-like hyaline inclusions were immunocytochemically and electron microscopically investigated in a patient with sporadic motor neuron disease. The hyaline inclusions were chiefly observed within the perikarya of both normal-looking and chromatolytic anterior horn cells in the lumbar spinal cord, but some were detected in the axons and dendrites. Usually, a single inclusion was found in the perikaryon, but in rare cases two or more were observed. Immunocytochemically, these inclusions were intensely immunostained with anti-ubiquitin antibody. Ultrastructurally, the hyaline inclusions were chiefly composed of randomly arranged linear structures associated with ribosome-like granules, varying from compactly arranged linear densities to more loosely packed ones. They contained scattered vesicles of various sizes and occasionally a focal accumulation of randomly arranged 10-nm neurofilaments or 13-25-nm filamentous structures.

摘要

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引用本文的文献

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Immunocytochemical and ultrastructural studies of hyaline inclusions in sporadic motor neuron disease.散发性运动神经元病中透明包涵体的免疫细胞化学和超微结构研究。
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本文引用的文献

1
The distribution of Lewy bodies in the central and autonomic nervous systems in idiopathic paralysis agitans.特发性帕金森病中路易小体在中枢神经系统和自主神经系统中的分布
J Neurol Neurosurg Psychiatry. 1960 Nov;23(4):283-90. doi: 10.1136/jnnp.23.4.283.
2
Fine structural study of neurofibrillary changes in a family with amyotrophic lateral sclerosis.肌萎缩侧索硬化症家族中神经原纤维变化的超微结构研究
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肌萎缩侧索硬化症中神经丝变化的超微结构观察
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Neurofibrillary axonal swellings and amyotrophic lateral sclerosis.
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Diffuse type of Lewy body disease: progressive dementia with abundant cortical Lewy bodies and senile changes of varying degree--a new disease?弥漫型路易体病:伴有大量皮质路易小体和不同程度老年改变的进行性痴呆——一种新疾病?
Clin Neuropathol. 1984 Sep-Oct;3(5):185-92.
6
Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells.家族性肌萎缩侧索硬化症。一个以累及后索和脊髓小脑束以及前角细胞出现透明包涵体为特征的亚组。
Arch Neurol. 1967 Mar;16(3):232-43. doi: 10.1001/archneur.1967.00470210008002.
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Ultrastructure of anterior horn motor neurones in the Hirano-Kurland-Sayre type of combined neurological system degeneration.
J Neurol Sci. 1971 Aug;13(4):389-99. doi: 10.1016/0022-510x(71)90002-5.
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Hereditary amyotrophic lateral sclerosis. Histochemical and electron microscopic study of hyaline inclusions in motor neurons.遗传性肌萎缩侧索硬化症。运动神经元中透明包涵体的组织化学和电子显微镜研究。
Arch Neurol. 1972 Oct;27(4):292-9. doi: 10.1001/archneur.1972.00490160020003.
9
Sporadic lower motor neuron disease with Lewy body-like inclusions: a new subgroup?伴有路易小体样包涵体的散发性下运动神经元病:一个新的亚组?
Acta Neuropathol. 1988;76(2):208-11. doi: 10.1007/BF00688105.
10
Ultrastructural study of chromatolytic neurons in an adult-onset sporadic case of amyotrophic lateral sclerosis.
Acta Neuropathol. 1988;75(5):523-8. doi: 10.1007/BF00687142.