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既往未接受化疗情况下急性髓系白血病与多发性骨髓瘤同时发生

Simultaneous occurrence of acute myelogenous leukaemia and multiple myeloma without previous chemotherapy.

作者信息

Matsuzaki H, Yamaguchi K, Hara H, Mitsuya H, Kawano F, Araki K, Tanaka R, Kishimoto S

出版信息

Scand J Haematol. 1983 Mar;30(3):278-86. doi: 10.1111/j.1600-0609.1983.tb01491.x.

Abstract

A patient with simultaneous occurrence of multiple myeloma and acute myelogenous leukaemia without previous chemotherapy was studied. Indirect immunofluorescence and protein A-coupled ox red blood cells rosette technique by use of anti-idiotype (Id) antibody showed some T cells with receptors of idiotypic specificity identical with that of the secreted myeloma protein. Plaque forming cell assay showed the presence of Id producing peripheral blood lymphocytes with EB virus receptor, probably B cells. These observations strongly suggest that multiple myeloma was not the result of a neoplastic transformation of the most differentiated B cells, plasma cell, but of lymphoid stem cells capable of differentiating to either B or T cells. However, there was not a detectable population of myeloblasts that expressed the same idiotype. Chromosomal analysis revealed a deletion of the long arm of chromosome 8 in myeloblasts but not in T or B cells. These results support the hypothesis of separate clonal origins for the leukaemic and myeloma components in this case.

摘要

对一名既往未接受过化疗、同时患有多发性骨髓瘤和急性髓性白血病的患者进行了研究。通过使用抗独特型(Id)抗体的间接免疫荧光和蛋白A偶联的牛红细胞玫瑰花结技术显示,一些T细胞具有与分泌的骨髓瘤蛋白相同的独特型特异性受体。空斑形成细胞试验显示存在具有EB病毒受体、可能是B细胞的产生Id的外周血淋巴细胞。这些观察结果强烈表明,多发性骨髓瘤不是最分化的B细胞即浆细胞发生肿瘤转化的结果,而是能够分化为B细胞或T细胞的淋巴干细胞的结果。然而,未检测到表达相同独特型的成髓细胞群体。染色体分析显示成髓细胞中8号染色体长臂缺失,而T细胞或B细胞中未缺失。这些结果支持了该病例中白血病和骨髓瘤成分具有独立克隆起源的假说。

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