An unusual case of indolent B-cell lymphoma with distinct chronic lymphocytic leukemia and marginal zone differentiation according to the site of involvement

被引:5
作者
Baseggio, L
Gazzo, S
Callet-Bauchu, E
Traverse-Glehen, A
Thieblemont, C
Bryon, PA
Magaud, JP
Berger, F
Felman, P
机构
[1] Ctr Hosp Lyon Sud, Serv Hematol Clin, F-69495 Pierre Benite, France
[2] Ctr Hosp Lyon Sud, Serv Hematol Biol, F-69495 Pierre Benite, France
[3] Ctr Hosp Lyon Sud, Serv Anat Pathol, F-69495 Pierre Benite, France
[4] Hop Edouard Herriot, Hematol Lab, Lyon, France
关键词
chronic lymphocytic leukemia; splenic marginal zone; B-cell lymphoma; immunophenotype; mutational status of IgV(H); del(13)( q14.3); expression gene;
D O I
10.1080/10428190500138039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The immunological pro. le of lymphoproliferative disorders is usually conserved whatever the involved site, thus allowing a reliable diagnosis from peripheral blood analysis, especially in small lymphocytic lymphoma/chronic lymphocytic lymphoma (SLL/CLL). Here we present a case wherein the cytology and immunophenotype of blood specimen and bone marrow argue in favor of SLL/CLL with a typical Matutes score (5/5), whereas the cyto-histology and immunophenotype of spleen specimen led to the diagnosis of splenic marginal zone B-cell lymphoma (SMZL). Moreover genomic analysis showed that the splenic cells displayed a SMZL signature. Whereas these data suggested the presence of 2 B-cell clones, the study of the mutational status of IgV(H) gene in blood and spleen demonstrated the presence of a single clone, which likely developed simultaneously along two distinct ways of differentiation according to the anatomic site suggesting here the predominant role of a micro-environmental factor in cell differentiation. Although rare, this kind of event must be kept in mind as a cause of discrepancies between diagnoses from different sites.
引用
收藏
页码:1369 / 1374
页数:6
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