期刊文献+

少突胶质细胞包涵体对多系统萎缩的诊断意义 被引量:2

Oligodendroglial cytoplasmic inclusion in multiple system atrophy
原文传递
导出
摘要 目的 观察多系统萎缩脑和脊髓内少突胶质细胞包涵体并评估其诊断意义。方法 应用Gallyas Braak银染色法研究 4例经临床和传统病理方法诊断的多系统萎缩的脑和脊髓标本 ,以 8例运动神经元病的脑和脊髓 ,6例无神经系统症状和病理改变的同龄人脑标本作对照。结果  4例病例中 3例的脑和脊髓白质发现少突胶质细胞包涵体 ,该包涵体位于少突胶质细胞胞质内 ,呈半月形、镰刀形、火焰形。主要分布于脑桥、小脑、苍白球 壳核、延髓白质纤维束 ,脊髓外侧束 ,且与髓鞘变性脱失的分布一致。另有 1例临床缺乏植物神经症状 ,黑质和脊髓中间外侧柱细胞无明显病变者 ,其脑和脊髓白质未观察到这种包涵体。所有对照病例的脑和脊髓白质内也未发现少突胶质细胞包涵体。结论 少突胶质细胞包涵体是散发性多系统萎缩特异性较高的病理标志 。 Objective To investigate the oligodendroglial cytoplasmic inclusion (OCI) in the central nervous system of multiple system atrophy (MSA) and to evaluate its roles in pathologic diagnosis of MSA.Methods Modified Gallyas Braak staining was used to investigate tissue samples of the brain and the spinal cord of 4 cases with MSA, which were previously diagnosed by clinical and routine pathologic methods. Eight cases with motor neuron disease and 6 cases without nervous system disease were used for control study.Results OCIs were demonstrated by Gallyas barrak method in the white matter of the brain and the spinal cord of 3 cases with MSA. They look like sickle , semilunar , and flame shaped. Their main distributions were transverse fibers of the basis pontine, the white matter of the cerebellum, striatopallidal fibers and lateral column of the spinal cord. While OCIs were not found in the brain and the spinal cord of one case without typical clinical features and pathologic findings. Nor did all of the control cases.Conclusions OCIs may be regarded as pathologic marker of the sporadic forms of MSA. It also suggests that OCIs are related to degenerative process of myelinated fibers in MSA.
出处 《中华神经科杂志》 CAS CSCD 北大核心 2002年第2期99-102,共4页 Chinese Journal of Neurology
基金 国家九七三课题资助项目 (G2 0 0 0 0 5 70 )
关键词 少突神经胶质 包涵体 多系统萎缩 诊断 Oligodendroglial Inclusion bodies Multiple system atrophy
  • 相关文献

参考文献9

  • 1Papp MI, Kahn JE, Lantos PL. Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy(striatonigral degeneration,olivopontocerebellar atrophy and Shy-Drager syndrome).J Neurol Sci,1989,94:79-100.
  • 2Nakazato Y, Yamazaki MT, Hirato J, et al. Oligodentroglial microtubular tangles in olivopontocerebellar atrophy.J Neuropathol Exp Neurol, 1990,49:521-530.
  • 3Murayama S, Arima K, NakazatoY, et al. Immunocytochemical and ultrastructural studies of neuronal and oligodendroglial cytoplasmic inclusions in multipe system atrophy 2. oliagdendroglial cytoplasmic inclusions. Acta Neuropathol ,1992,84:32-38.
  • 4Kobayashi K, Miyazu K, Katsukawa K,et al. Cytoskeletal protein abnormalities in patients with olivopontocerebellar atrophy--an immunocytochemical and Gallyas silver impregnation study.J Neuropathol Appl Neurobiol, 1992,18:237-249.
  • 5Mochzuki A, Mizusawa H, Ohkoshi N, et al. Argentophilic intracytoplasmic inclusions in multiple system atrophy.J Neurol, 1992,239:311-316.
  • 6Papp MI, Lantos PL. Accumulation of tubular structures in oligodendroglial and neuronal cells as the basic alteration in multiple system atrophy.J Neurol Sci,1992,107:172-182.
  • 7Papp MI, Lantos PL. The distribution of oligdendrglial iuclusions in multiple system atrophy and its relevance to clinical symptomatology. Brain,1994,117:235-243.
  • 8杨佐濂,朱克.神经系统多系统萎缩二例临床及病理报告[J].中华神经科杂志,1999,32(3):192-192. 被引量:1
  • 9Braak H, Braak E, Ohm T. Silver impregnation of Alzheimer′s neurofibrillary changes counterstained for basophilic material and lipofusin pigment . Stain Technol ,1988,63:197-200.

同被引文献41

  • 1夏程,郎森阳.多系统萎缩的临床分型和影像学改变特点分析[J].中华神经科杂志,2007,40(10):687-689. 被引量:13
  • 2Piao YS, Wakabayashi K, Kakita A, et al. Neuropathology with clinical correlations of sporadic amyotrophic lateral sclerosis: 102 autopsy cases examined between 1962 and 2000 [ J ]. Brain Pathol, 2003,13 ( 1 ) : 10-22.
  • 3Ahmed Z, Asi YT, Sailer A, et al. The neuropathology, pathophysiology and genetics of multiple system atrophy [ J ]. Neuropathol Appl Neurobiol, 2012,38( 1 ) :4-24.
  • 4Dugger BN, Hidalgo JA, Chiarolanza G,et al. The distribution of phosphorylated tau in spinal cords of Alzheimer's disease and non- demented individuals E J ]. J Alzheimers Dis, 2013,34 ( 2 ) : 529- 536.
  • 5Del Trediei K, Braak H. Spinal cord lesions in sporadic Parkinson's disease[ J]. Acta Neuropathol, 2012, 124 (5) :643- 664.
  • 6Vitaliani R, Scaravilli T, Egarter-Vigl E,et al. The pathology of the spinal cord in progressive supranuclear palsy [ J ]. J Neuropathol Exp Neurol, 2002,61 (3) :268-274.
  • 7Ince PG, Lowe J, Shaw PJ. Amyotrophic lateral sclerosis : current issues in classification, pathogenesis and molecular pathology [ J]. Neuropathol Appl Neurobiol, 1998,24 ( 2 ) : 104-117.
  • 8Brettschneider J, Arai K, Del Tredici K, et al. TDP43 pathology and neuronal loss in amyotrophic lateral sclerosis spinal cord [ J]. Acta Neuropathol, 2014,128 ( 3 ) :423 437.
  • 9Trojanowski JQ, Revesz T; Neuropathology Working Group on MSA. Proposed neuropathological criteria for the post mortem diagnosis of multiple system atrophy [ J ]. Neuropathol Appl Neurobiol, 2007,33(6) :615-620.
  • 10黄克维,王鲁宁.神经系统病理剖检技术[M]//黄克维,吴丽娟.临床神经病理学.北京:人民军医出版社,1999:282-287.

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部