Finch C N, Nichols M, Shrimpton A, Liu D, Hutchison R E
Department of Pathology, State University of New York Upstate Medical University, Syracuse, New York 13210, USA.
Arch Pathol Lab Med. 2000 Dec;124(12):1816-9. doi: 10.5858/2000-124-1816-PNMZBC.
Primary nodal marginal zone B-cell lymphoma is an uncommon monoclonal B-cell lymphoproliferative disorder. We report a case of a 79-year-old woman who presented with generalized lymphadenopathy. Histologic and immunohistochemical examinations of biopsy sections from an axillary lymph node were consistent with nodal marginal zone B-cell lymphoma. Flow cytometry analysis showed 2 distinct clonal B-cell populations expressing lambda or kappa light chain restriction. Subsequently, genomic deoxyribonucleic acid (DNA) isolated from a paraffin-embedded lymph node section was analyzed for the presence of gene rearrangements. Polymerase chain reaction (PCR) analysis of immunoglobulin heavy chain genes revealed 3 rearranged DNA bands, confirming the presence of more than one clonal B-cell population. These immunophenotypic and genotypic findings have not been previously described in association with this type of lymphoma. To our knowledge, this represents the first reported case of biclonal nodal marginal zone B-cell lymphoma.
原发性淋巴结边缘区B细胞淋巴瘤是一种罕见的单克隆B细胞淋巴增殖性疾病。我们报告一例79岁女性,表现为全身淋巴结肿大。对腋窝淋巴结活检切片进行组织学和免疫组化检查,结果符合淋巴结边缘区B细胞淋巴瘤。流式细胞术分析显示2个不同的克隆性B细胞群体,表达λ或κ轻链限制性。随后,对从石蜡包埋的淋巴结切片中分离的基因组脱氧核糖核酸(DNA)进行基因重排分析。免疫球蛋白重链基因的聚合酶链反应(PCR)分析显示3条重排的DNA条带,证实存在不止一个克隆性B细胞群体。这些免疫表型和基因分型结果此前尚未与这种类型的淋巴瘤相关联进行描述。据我们所知,这是首例报道的双克隆性淋巴结边缘区B细胞淋巴瘤病例。