Said J W, Hargreaves H K, Pinkus G S
Cancer. 1979 Aug;44(2):504-28. doi: 10.1002/1097-0142(197908)44:2<504::aid-cncr2820440221>3.0.co;2-h.
Ultrastructural studies were performed on 40 B-cell and 14 T-cell lymphomas of non-Hodgkin's type (NHL). Most B-cell lymphomas were comprised of neoplastic cells with morphologic features compatible with a follicular center cell origin. Dendritic reticulum cells and their desmosome-associated processes, characteristic of germinal centers, were observed in all 11 cases of nodular poorly differentiated lymphocytic lymphoma and in one of two cases of nodular "histiocytic" lymphoma, but were not identified in the lymphomas with a diffuse growth pattern. Desmosomes were observed between dendritic reticulum cells and were not found between lymphoid cells. Large neoplastic cells comprising lymphomas of "histiocytic," mixed lymphocytic "histiocytic," and "undifferentiated" types were characterized ultrastructurally and immunologically as lymphoid cells. Malignant lymphomas of well and moderately well differentiated lymphocytic types (7 cases) revealed B-cell markers, and represented a distinct homogenous group of neoplasms, with electron microscopic features most closely resembling follicular cuff lymphocytes. T-cell malignancies included lymphoblastic lymphomas (3 cases), large cell ("histiocytic") lymphomas (4 cases), lymphoepithelioid cell ("Lennert's") lymphomas (2 cases), mycosis fungoides (3 cases) and diffuse poorly differentiated lymphocytic lymphomas (2 cases). A consistent finding in the T-cell proliferations was the presence of small and/or large lymphoid cells with extremely irregular and/or convoluted nuclei, which occurred in varying proportions and with variable degrees of nuclear complexity. The nuclear irregularity evident in the neoplastic T cells was distinguishable from that observed for lymphoid cells of B-cell lymphomas. In comparing the cytoplasmic features of the T- and B-cell neoplasms ultrastructurally, the only distinguishing feature was the presence of well developed granular endoplasmic reticulum with dilated cisternae, i.e., plasmacytoid features, predictive of a B cell origin.
对40例非霍奇金氏型(NHL)B细胞淋巴瘤和14例T细胞淋巴瘤进行了超微结构研究。大多数B细胞淋巴瘤由具有与滤泡中心细胞起源相符的形态学特征的肿瘤细胞组成。在所有11例结节性低分化淋巴细胞淋巴瘤以及2例结节性“组织细胞性”淋巴瘤中的1例中观察到了生发中心特有的树突状网状细胞及其桥粒相关突起,但在弥漫性生长模式的淋巴瘤中未发现。在树突状网状细胞之间观察到了桥粒,而在淋巴细胞之间未发现。构成“组织细胞性”、混合淋巴细胞“组织细胞性”和“未分化”型淋巴瘤的大肿瘤细胞在超微结构和免疫方面被鉴定为淋巴细胞。高分化和中分化淋巴细胞型恶性淋巴瘤(7例)显示B细胞标志物,代表一组独特的同质肿瘤,其电子显微镜特征与滤泡套淋巴细胞最为相似。T细胞恶性肿瘤包括淋巴母细胞淋巴瘤(3例)、大细胞(“组织细胞性”)淋巴瘤(4例)、淋巴上皮样细胞(“ Lennert氏”)淋巴瘤(2例)、蕈样霉菌病(3例)和弥漫性低分化淋巴细胞淋巴瘤(2例)。T细胞增殖中一致的发现是存在小和/或大的淋巴细胞,其核极其不规则和/或卷曲,以不同比例出现且核复杂程度不同。肿瘤性T细胞中明显的核不规则与B细胞淋巴瘤的淋巴细胞中观察到的核不规则不同。在超微结构上比较T细胞和B细胞肿瘤的细胞质特征时,唯一的区别特征是存在发达的颗粒内质网,其池扩张,即浆细胞样特征,提示B细胞起源。