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一例多发性骨髓瘤,有两个亚克隆分别产生κ链和缺陷γ链。

A case of multiple myeloma with two subclones producing separately kappa and defective gamma chains.

作者信息

Metz K, Leder L D

出版信息

Cancer. 1985 Sep 15;56(6):1392-5. doi: 10.1002/1097-0142(19850915)56:6<1392::aid-cncr2820560629>3.0.co;2-7.

Abstract

A case of multiple myeloma is described that contained two morphologically identical but immunologically diverse subpopulations. One of the subclones produced only kappa chains, whereas the other contained only gamma chains. Additional immunohistologic investigations revealed production by one of the subpopulations of defective gamma chains that were devoid of demonstrable Fd parts. It could not be decided whether this was due to a structural or an antigenetical defect. Furthermore, only the kappa-producing subclone exhibited J-chains. Based upon these findings and their possible cause and on respective findings concerning other B-cell neoplasias, it is concluded that the consequent application of an ever-increasing number of different immunologic markers, in order to better classify malignant lymphomas, will eventually result in the reverse, namely, in a complete breakup of this group of malignancies into individual cases.

摘要

本文描述了一例多发性骨髓瘤病例,该病例包含两个形态相同但免疫表型不同的亚群。其中一个亚克隆仅产生κ链,而另一个仅包含γ链。进一步的免疫组织学研究显示,其中一个亚群产生的γ链存在缺陷,缺乏可检测到的Fd部分。无法确定这是由于结构缺陷还是抗原缺陷所致。此外,只有产生κ链的亚克隆表达J链。基于这些发现及其可能的原因,以及关于其他B细胞肿瘤的相应发现,得出结论:为了更好地对恶性淋巴瘤进行分类而不断增加使用不同免疫标志物的做法,最终可能会导致相反的结果,即将这组恶性肿瘤完全细分为一个个单独的病例。

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