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中线非何杰金氏恶性淋巴瘤的超微结构研究 被引量:1

Midline Non-Hodgkin's Malignant Lymphoma,Uitrastructural Study
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摘要 本文报告了18例中线非何杰金氏恶性淋巴瘤电镜研究结果,其中T细胞型16例,B细胞型2例。18例中多形细胞型14例,透明细胞型、小淋巴细胞型、无裂细胞型及裂细胞型各1例。多形细胞型中的大、中型瘤细胞中有较丰富、畸形的内质网,线粒体扩张,嵴减少或消失而表现出异形性;大型瘤细胞的核大,常染色质丰富和易见的核仁均说明其蛋白质合成机能旺盛,瘤细胞增生活跃。瘤组织中大、中型细胞越多,其恶性度越高。透明细胞型以大、中型细胞为主,显示出其高度恶性。无裂细胞型以不规则细胞突起文错存在而表现为瘤细胞成团存在,形成滤泡样结构,限制其瘤细胞的浸润、迁移,其恶性度较弥漫性增生者为低。相反后者则易于扩散、浸润,预后差。 Eighteen cases of midline Non- Hodgkin's malignant lymphomas were studied using electron mi- croscopy. The results indicated that 1 6 cases,of midline Non- Hodgkin's malignant ly mphomas were Tcell lymphomas and the other 2 cases were Bcell lymphomas.According to project of clinical classifi-eation about Non- Hodgkin's lymphoma,14 cases were pleomorphism type;the other 4 cases were hyalocyte((clear cell)small lymphocyte schistocyte and un-schistocyte type。There were deforma-tional and richer endoplasmic reticulum(ER)in large and medium cells of the pleomorphism and its mitochon drion expended and mitochondrial crista reduced or disappeared.The exu berant protein oflarge cell was to be compound in which showin8 (appearing)larger nudeus,clearner nucleolus andricher autosome。The more there were large and medium cells in tumour tissue,the more malig nanttumour was.The large and medium cells were main cell of hga locyte type existing a ball un-schisto-cyte had unregular cell process,and formed follicle structure. The structure would control diffusion oftumour cells on the contrary,non-follicular type is more malignant than follicular type at spread oflymphoma.
出处 《新疆医学院学报》 1994年第3期211-215,共5页
关键词 非何杰金氏 淋巴瘤 超微结构 non- Hodgkin's lymphoma ultrustructure
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二级参考文献2

  • 1Su I J,Lymphoma,1992年,7卷,1/2期,47页
  • 2刘卫平,中华病理学杂志,1986年,15卷,3期,183页

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  • 1Resnitzky P, Matutes E, Hedges M, et al. The ultrastructure of mantle cell lymphoma and other B-cell disorders with translocation t (11; 14 )(q13;q32) [J]. Br J Haematol, 1996, 94(2): 352 -361.
  • 2Trivedi N S, Wang H W, Nieminen A L, et al. Quantitative analysis of Pc 4 localization in mouse lymphoma (LY-R) cells via double-label confoeal fluorescence microscopy [J]. Photochem Photobiol, 2000, 71(5): 634 - 639.

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