肌萎缩侧索硬化
前角细胞
脊髓
病态的
锥体束
神经突
病理
医学
皮质脊髓束
退行性疾病
解剖
变性(医学)
神经科学
生物
疾病
磁共振成像
生物化学
放射科
磁共振弥散成像
体外
作者
Dirk Troost,Elisabeth S. Louwerse,J.M.B.V. de Jong,G. S. D. Van Leersum,John A. van Raalte
出处
期刊:PubMed
日期:1989-05-01
卷期号:8 (3): 152-5
被引量:2
摘要
A case of amyotrophic lateral sclerosis revealed the classical pathologic features of ALS, i.e. neuronal loss in the anterior horns and pyramidal tract degeneration. In addition to the pathological hallmarks of Alzheimer's disease, senile plaques, neurofibrillary tangles and granulovacuolar changes of neurons were also present. Clinically the 67-year-old patient exhibited ALS of the upper extremity and a mild forgetfulness. Two striking pathological features were noted in the spinal cord: first, at several levels in the spinal cord excessive amounts of myelinated neurites were found; second, the microglial proliferation in the anterior horns was very intense and positive for leukocyte common antigen.
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