J-chain-producing immunoblastic lymphoma in a case of Richter's syndrome. Immunohistochemical evidence for a gradual malignant transformation of a single B-cell clone and flow cytophotometric data.

P Möller, G E Feichter, D Fritze, D Haag, B Schüle
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引用次数: 7

Abstract

A 66-year old male with Richter's syndrome died 52 month after diagnosis of chronic lymphocytic leukaemia (CLL). The clinical course was characterized by a marked IgM hypoglobulinaemia which paralleled a chronically relapsing Herpes simplex infection. Autopsy showed a large retroperitoneal and intraabdominal tumour mass and well defined supradiaphragmatic lymphomas. Histological examination revealed a composite tumour consisting of CLL B-cell type (B-CLL) and immunoblastic malignant lymphoma of B-cell type (B-IbL). The lymphocytes bear mu-chains on their surface and to a lesser extend within their cytoplasm, the obviously defective immunoblasts produce J chains exclusively. Flow cytophotometric data seem to indicate an identical diploid stem line of the two tumours. The majority of the cells are in G0/1 phase. The CLL rarely produces mitoses, however, the IbL has a mitotic rate of 7% and a considerable proportion (33%) of cells in the phase of DNA-synthesis. This is the fourth malignant lymphoma and the second immunoblastic lymphoma to be reported that produces J chain in the absence of immunoglobulin.

里希特氏综合征一例产生j链的免疫母细胞淋巴瘤。单个b细胞克隆逐渐恶性转化的免疫组织化学证据和流式细胞光度测定数据。
一位66岁男性里希特氏综合征患者在诊断为慢性淋巴细胞白血病(CLL) 52个月后死亡。临床过程的特点是明显的IgM低球蛋白血症,与慢性复发的单纯疱疹感染平行。尸检显示一个大的腹膜后和腹内肿瘤团块和清晰的膈上淋巴瘤。组织学检查显示为CLL b细胞型(B-CLL)和b细胞型免疫母细胞恶性淋巴瘤(B-IbL)组成的复合型肿瘤。淋巴细胞表面有mu链,细胞质内有较少的J链,明显缺陷的免疫母细胞只产生J链。流式细胞光度法数据似乎表明两个肿瘤具有相同的二倍体茎系。大多数细胞处于G0/1期。CLL很少产生有丝分裂,然而,IbL有丝分裂率为7%,相当比例(33%)的细胞处于dna合成阶段。这是在缺乏免疫球蛋白的情况下产生J链的第四例恶性淋巴瘤和第二例被报道的免疫母细胞淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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