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Southern blot analysis in a case of Richter's syndrome. Evidence for a postrearrangement heavy chain gene deletion associated with the altered phenotype.

作者信息

Schots R, Dehou M F, Jochmans K, Heirman C, de Waele M, van Camp B, Thielemans K

机构信息

Department of Hematology and Immunology, Faculty of Medicine, Vrije Universiteit Brussel, Belgium.

出版信息

Am J Clin Pathol. 1991 Apr;95(4):571-7. doi: 10.1093/ajcp/95.4.571.

DOI:10.1093/ajcp/95.4.571
PMID:1849702
Abstract

Richter's syndrome (RS) can be defined as the emergence of an aggressive lymphoma in patients suffering from chronic lymphocytic leukemia (CLL). The authors performed immunophenotypic and Southern blot analysis of the peripheral blood and tissue specimen of a patient with RS. Using immunoperoxidase and immunogold-silver staining techniques and a panel of monoclonal antibodies, the authors found that the large cells characteristic of RS showed an altered immunophenotype as compared with the CLL cells and did not express mu heavy chain. Southern blot analysis revealed identical kappa light chain rearrangements in both tumoral cell populations consistent with a common clonal origin. Using the JH probe and several restriction enzymes, the authors also found evidence for a postrearrangement deletion of the heavy chain mu gene. These findings suggest that in this case of RS, a deletion of the heavy chain mu gene resulted in loss of mu expression by the larger cells that were characteristic of RS and was associated with their altered phenotype.

摘要

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引用本文的文献

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2
Composite low grade B-cell lymphomas with two immunophenotypically distinct cell populations are true biclonal lymphomas. A molecular analysis using laser capture microdissection.具有两个免疫表型不同细胞群的复合性低级别B细胞淋巴瘤是真正的双克隆淋巴瘤。使用激光捕获显微切割的分子分析。
Am J Pathol. 1999 Jun;154(6):1857-66. doi: 10.1016/S0002-9440(10)65443-0.
3
Clonal evolution of B cells in transformation from low- to high-grade lymphoma.
B细胞从低度淋巴瘤向高度淋巴瘤转化过程中的克隆进化。
Eur J Immunol. 1999 Apr;29(4):1253-64. doi: 10.1002/(SICI)1521-4141(199904)29:04<1253::AID-IMMU1253>3.0.CO;2-8.