Turesson I, Grubb A
Acta Med Scand. 1978;204(6):445-51. doi: 10.1111/j.0954-6820.1978.tb08472.x.
This report concerns six cases of multiple myeloma characterized by either no demonstrable monoclonal immunoglobulin in plasma or urine or by trace amounts (less than or equal to 0.1 g/l) of monoclonal kappa chains in the urine. In all cases there was an infiltration of the bone marrow by plasma cells containing kappa chains but no heavy chains. A retrospective analysis was made of 126 consecutive cases of Bence Jones myeloma. The number of kappa and lambda cases was approximately the same. All cases secreting less than or equal to 0.1 g light chains per 1 urine were of kappa type. This contrasts with a kappa/lambda ratio of 1.4-1.9 among reported series of M-components containing both heavy and light chains. A review of reported cases of non-secretory myeloma revealed a preserved capacity for Ig synthesis in the majority of cases and among these a preponderance of kappa chain producing clones. These observations might be explained by a higher tendency for kappa chain producing cells to mutate to low secretors or to cells producing abnormal light chains which are catabolized rapidly. The clinical data from our patients do not indicate a more pessimistic prognosis in non- or low-secretory myeloma, than in other cases of multiple myeloma.
本报告涉及6例多发性骨髓瘤病例,其特征为血浆或尿液中无可检测到的单克隆免疫球蛋白,或尿液中存在微量(小于或等于0.1 g/l)的单克隆κ链。所有病例中,骨髓均有含κ链但无重链的浆细胞浸润。对126例连续的本-周氏骨髓瘤病例进行了回顾性分析。κ型和λ型病例数量大致相同。所有每24小时分泌小于或等于0.1 g轻链的病例均为κ型。这与报道的同时含有重链和轻链的M成分系列中κ/λ比值为1.4 - 1.9形成对比。对报道的非分泌型骨髓瘤病例的回顾显示,大多数病例中免疫球蛋白合成能力保留,其中产生κ链的克隆占优势。这些观察结果可能是由于产生κ链的细胞更容易突变为低分泌细胞或产生快速分解代谢的异常轻链的细胞。我们患者的临床数据并未表明非分泌型或低分泌型骨髓瘤的预后比其他多发性骨髓瘤病例更悲观。