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淋巴细胞淋巴瘤中的双克隆IgA和IgM丙种球蛋白病

Biclonal IgA and IgM gammopathy in lymphocytic lymphoma.

作者信息

Weinstein S, Jain A, Bhagavan N V, Scottolini A G

出版信息

Clin Chem. 1984 Oct;30(10):1710-2.

PMID:6434203
Abstract

We report the case of a 76-year-old white man with a diffuse, well-differentiated lymphocytic lymphoma at the base of his tongue. Although serum electrophoresis, immunoelectrophoresis, and immunofixation showed he had a biclonal IgA kappa and IgM kappa gammopathy, biopsy of the tumor showed a positive immunoperoxidase response only for IgM kappa. The biclonal pattern persisted after chemotherapy, despite shrinkage of the tumor mass. The association of IgA and IgM appears to be the least frequent combination of separate biclonal immunoglobulins, the clinical course of such patients being more often that of lymphoma or macroglobulinemia than of myeloma. However, the symptomatology can be highly variable, as our case uniquely demonstrates.

摘要

我们报告了一例76岁白人男性病例,其舌根部患有弥漫性、高分化淋巴细胞淋巴瘤。尽管血清电泳、免疫电泳和免疫固定显示他存在双克隆性IgA κ和IgM κ丙种球蛋白病,但肿瘤活检显示仅IgM κ的免疫过氧化物酶反应呈阳性。尽管肿瘤肿块缩小,但化疗后双克隆模式仍持续存在。IgA和IgM的关联似乎是单独双克隆免疫球蛋白中最不常见的组合,此类患者的临床病程更常表现为淋巴瘤或巨球蛋白血症,而非骨髓瘤。然而,正如我们的病例独特显示的那样,症状可能高度多变。

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