Balázs L, István L, Marton E, Kádas L, Kelényi G
Acta Med Acad Sci Hung. 1980;37(3):253-60.
In a 34-year-old woman a non-Hodgkin malignant lymphoma with extreme splenomegaly and monoclonal IgM paraproteinaemia was seen. The removed spleen and splenic hilar lymph glands showed a nodular centroblastic-centrocytic malignant lymphoma with large numbers of plasmocytoid cells containing monotypical (monoclonal) IgM-kappa type immunoglobulin. The case represents a borderline non-Hodgkin malignant lymphoma with features of a follicular tumour and an immunocytoma. The appearance of peculiar intracytoplasmic inclusions would support this assumption. Therapeutic measures (splenectomy and/or cytostatic treatment) and prognostic features (nodularity of the tumour) are discussed.
在一名34岁女性中,发现了一例非霍奇金恶性淋巴瘤,伴有极度脾肿大和单克隆IgM副蛋白血症。切除的脾脏和脾门淋巴结显示为结节性中心母细胞-中心细胞性恶性淋巴瘤,有大量含有单型(单克隆)IgM-κ型免疫球蛋白的浆细胞样细胞。该病例代表了一种具有滤泡性肿瘤和免疫细胞瘤特征的边缘性非霍奇金恶性淋巴瘤。特殊胞质内包涵体的出现支持这一假设。文中讨论了治疗措施(脾切除术和/或细胞抑制治疗)及预后特征(肿瘤的结节性)。