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非霍奇金淋巴瘤中的DNA——一项细胞光度学研究。

DNA in non Hodgkin-lymphoma--a cytophotometric study.

作者信息

Sandritter W, Grimm H

出版信息

Beitr Pathol. 1977 Jul;160(3):213-30. doi: 10.1016/s0005-8165(77)80048-6.

Abstract

Cytophotometric DNA determinations on 26 cases of non-Hodgkin's lymphoma yielded the following findings: 1. Follicular centrocytic/centroblastic lymphomas (M. Brill-Symmers) and diffuse centrocytic lymphomas (lymphocytic lymphosarcoma) have a diploid DNA stem line. Diploid DNA values are observed in benign tumors, so that the assignment of these lymphomas to the group of "low grade malignancies" appears justified. 2. Lymphoblastic sarcomas show an aneuploid DNA stem line, as do 96% of all malignant tumors. 3. Lymphoid cells, plasma cells, and immunoblasts seen in immunocytomas are aneuploid. Thus these lymphomas must belong to the group of "high-grade malignant lymphomas" as regards their DNA distribution. 4. Immunoblastic sarcomas have aneuploid DNA stem lines (1 case tetraploid), in which both the lymphoid cells and the plasma cells from those immunoblastic sarcomas arising from immunocytomas show atypical DNTA distribution patterns. 5. In two cases of angioimmunoblastic lymphadenopathy, the lymphoid cells, plasma cells, and immunoblasts are aneuploid. They are thus regarded as "high grade malignancy" lymphomas. The results are discussed with respect to clinical course and prognosis. Measurements on a larger series of cases and correlation to clinical data are needed to support these results. Ultrafast DNA measurements made by flow-through cytophotometry can perhaps be helpful in the future for making the decision between a "low" or "high" grade malignant lymphoma.

摘要

对26例非霍奇金淋巴瘤进行细胞光度法DNA测定,结果如下:1. 滤泡中心细胞性/中心母细胞性淋巴瘤(布里尔-西默斯病)和弥漫性中心细胞性淋巴瘤(淋巴细胞性淋巴肉瘤)具有二倍体DNA干系。在良性肿瘤中观察到二倍体DNA值,因此将这些淋巴瘤归为“低度恶性肿瘤”组似乎是合理的。2. 淋巴母细胞肉瘤显示非整倍体DNA干系,所有恶性肿瘤中有96%也是如此。3. 免疫细胞瘤中所见的淋巴细胞、浆细胞和免疫母细胞是非整倍体。因此,就其DNA分布而言,这些淋巴瘤必定属于“高度恶性淋巴瘤”组。4. 免疫母细胞肉瘤具有非整倍体DNA干系(1例为四倍体),在由免疫细胞瘤发生的那些免疫母细胞肉瘤中,淋巴细胞和浆细胞均显示非典型DNA分布模式。5. 在2例血管免疫母细胞性淋巴结病中,淋巴细胞、浆细胞和免疫母细胞是非整倍体。因此,它们被视为“高度恶性”淋巴瘤。结合临床病程和预后对结果进行了讨论。需要对更多病例进行测量并与临床数据进行关联以支持这些结果。通过流动式细胞光度法进行的超快速DNA测量或许将来有助于判定是“低度”还是“高度”恶性淋巴瘤。

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