Syrjänen K J
Arch Geschwulstforsch. 1979;49(4):289-98.
A diffuse generalized lymphoma histologically classified as mixed histiocytic-lymphocytic type and associated with profound immunologie abnormalities is reported. The patient had an autoimmune hemolytic anemia, an autoimmune thrombocytopenia, polyclonally increased IgG and IgM, polyclonal secretion of kappa and lamda chains into urine, very low serum complement C3 and antibodies against glomerulus and smooth muscle. When studied with the modern surface-marker techniques, the lesion was found to be composed of entirely lymphoid cells of the B-lymphocyte series. The proper classification of this tumor could be a primitive immunoblastic sarcoma. The relationship of the present tumor to the non-neoplastic angioimmunoblastic lymphadenopathia is discussed. The necessity of applying the surface-marker techniques in the classification of malignant lymphomas is emphasized.
本文报道了一例组织学分类为混合组织细胞 - 淋巴细胞型且伴有严重免疫异常的弥漫性全身性淋巴瘤。该患者患有自身免疫性溶血性贫血、自身免疫性血小板减少症、IgG和IgM多克隆性升高、κ和λ链多克隆分泌至尿液中、血清补体C3极低以及抗肾小球和抗平滑肌抗体。采用现代表面标志物技术研究时,发现该病变完全由B淋巴细胞系列的淋巴细胞组成。该肿瘤的恰当分类可能是原始免疫母细胞肉瘤。文中讨论了目前该肿瘤与非肿瘤性血管免疫母细胞性淋巴结病的关系。强调了在恶性淋巴瘤分类中应用表面标志物技术的必要性。