Stramignoni A, Carbonara A, Paolino W, Navone R, Coda R, Leonardo E
J Cancer Res Clin Oncol. 1980 Jan;96(1):93-103. doi: 10.1007/BF00412900.
Clinicopathological ultrastructural, and immunohistochemical findings of a new case of IgG1 heavy chain disease are reported in detail. The abnormal protein lacks the VH and CH1 region with sequence starting at 225 residue. The main pathologic feature was plasmacytic tumor of the lymph nodes with B-cell immunoblastic sarcoma patterns. Neoplastic diffusion to other organs was also present. Plasmacytic neoplastic cells have also been found in the bone marrow. The ultrastructure of the noeplastic cells was characterized by more or less abundant plasmacytic-like endoplasmic reticulum with very frequent peculiar whorled configurations. Immunohistochemical methods revealed the abnormal protein production by neoplastic cells in different stages of differentiation. From this case and from the data of the literature it is concluded that the gamma HCD is due to a neoplastic proliferation of lymphoplasmacytic cells whereas the reticulum cells are never involved.
详细报告了一例新的IgG1重链病的临床病理、超微结构和免疫组化结果。异常蛋白缺乏VH和CH1区域,序列从第225个残基开始。主要病理特征为具有B细胞免疫母细胞肉瘤模式的淋巴结浆细胞瘤。肿瘤也扩散到了其他器官。骨髓中也发现了浆细胞性肿瘤细胞。肿瘤细胞的超微结构特征是或多或少丰富的浆细胞样内质网,伴有非常频繁的特殊涡旋状结构。免疫组化方法显示肿瘤细胞在不同分化阶段产生异常蛋白。从该病例和文献数据得出结论,γ重链病是由于淋巴浆细胞的肿瘤性增殖,而网状细胞从不参与。