慢性淋巴细胞白血病
癌症研究
医学
CD5型
CD20
病理
IGHV@
淋巴瘤
白血病
作者
Fumihiro Ishida,Hideyuki Nakazawa,Yuka Takezawa,Kazuyuki Matsuda,Naoko Asano,Kenji Sano,Hitoshi Sakai,Toshiro Ito
出处
期刊:Journal of Clinical and Experimental Hematopathology
[Japanese Society for Lymphoreticular Tissue Research]
日期:2013-08-01
卷期号:53 (2): 157-160
被引量:7
摘要
Richter syndrome (RS) involves the development of an aggressive lymphoma in patients with chronic lymphocytic leukemia (CLL). Diffuse large B-cell lymphoma (DLBCL) is the most common type of RS. Extranodal RS occasionally occurs; however, isolated lesions in the central nervous system (CNS) of RS are rarely seen and the features have not been well described. We describe a Japanese patient who developed isolated involvements of the parenchyma of the CNS as a manifestation of RS two years after the initial diagnosis of CLL. DLBCL in the cerebrum was confirmed to be clonally related to the CLL cells by immunoglobulin heavy chain (IGH) gene analysis, utilizing the identical VH-D-J regions with additional mutations in the IGH variable region.
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