Jellinger K, Slowik F, Sluga E
Clin Neurol Neurosurg. 1979;81(3):173-84. doi: 10.1016/0303-8467(79)90005-2.
Cytochemical and electron microscopical studies in six cases of primary intracranial malignant lymphomas, four of which were diagnosed by biopsy, confirmed their ultrastructural identity with extraneural malignant lymphomas classified as immunoblastomas and immunocytomas. Demonstration of transformation of 'blast-like' cells (immunoblasts) toward rough E. R. developing cells in all these tumours argue for the B-dell origin of these types of cerebral lymphomas, previously referred to as reticulum cell sarcomas/microgliomas. CSF studies showed increased levels of B cells with surface IgG in two cases of immunoblastoma, and increased IgG levels with light chains in two cases each immunoblastoma and of pleomorphic immunocytoma, while one case of immunoblastoma showed a normal T cell to B cell ratio with increased monoclonal and surface, IgM suggesting some morphological and immunological heterogeneity of these lymphomas.
对6例原发性颅内恶性淋巴瘤进行了细胞化学和电子显微镜研究,其中4例经活检确诊,证实其超微结构与分类为免疫母细胞瘤和免疫细胞瘤的神经外恶性淋巴瘤相同。在所有这些肿瘤中,“母细胞样”细胞(免疫母细胞)向粗面内质网发育细胞的转化表明这些类型的脑淋巴瘤起源于B细胞,以前称为网状细胞肉瘤/小胶质细胞瘤。脑脊液研究显示,2例免疫母细胞瘤患者的B细胞表面IgG水平升高,2例免疫母细胞瘤和2例多形性免疫细胞瘤患者的IgG轻链水平升高,而1例免疫母细胞瘤患者的T细胞与B细胞比例正常,但单克隆和表面IgM增加,提示这些淋巴瘤存在一些形态学和免疫学异质性。