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伴单克隆丙种球蛋白病的结节性混合细胞淋巴瘤

Nodular mixed cell lymphoma with monoclonal gammopathy.

作者信息

Bain G O, Belch A

出版信息

Am J Clin Pathol. 1981 Dec;76(6):832-7. doi: 10.1093/ajcp/76.6.832.

Abstract

Malignant lymphomas are rarely accompanied by a serum M component. Such neoplasms are usually of lymphocytic cell type and, with extremely rare exceptions, of diffuse pattern. A patient with an unusual malignant lymphoma of mixed cell type characterized by follicular structures and vascular proliferation was found to have a serum monoclonal gammopathy (IgM kappa) of over 4 g/dl. Remission accompanied by a pronounced reduction in the M protein was achieved with Chlorambucil. Subsequent relapse was characterized by the emergence of a large cell lymphoma with IgM kappa surface immunoglobulin. No concomitant rise in the serum M component accompanied relapse.

摘要

恶性淋巴瘤很少伴有血清M成分。这类肿瘤通常是淋巴细胞型,并且除了极少数例外,呈弥漫性分布。一名患有以滤泡结构和血管增生为特征的不寻常混合细胞型恶性淋巴瘤患者,被发现有超过4g/dl的血清单克隆丙种球蛋白病(IgM κ)。使用苯丁酸氮芥后病情缓解,同时M蛋白显著减少。随后的复发表现为出现带有IgM κ表面免疫球蛋白的大细胞淋巴瘤。复发时血清M成分没有相应升高。

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