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

作者信息

Baseggio Lucile, Gazzo Sophie, Callet-Bauchu Evelyne, Traverse-Glehen Alexandra, Thieblemont Catherine, Bryon Paul-André, Magaud Jean-Pierre, Berger Françoise, Felman Pascale

机构信息

Service d'Hématologie Biologique, Hôpital Edouard Herriot, Lyon, France.

出版信息

Leuk Lymphoma. 2005 Sep;46(9):1369-74. doi: 10.1080/10428190500138039.

Abstract

The immunological profile 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 IgVH 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.

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