Fernández-Solá J, Cases A, Monforte R, Pedro-Botet J C, Estruch R, Grau J M, Urbano-Márquez A
Acta Haematol. 1987;77(4):231-3. doi: 10.1159/000206001.
A case of a 44-year-old man in whom kappa light chain multiple myeloma and rhabdomyolysis (RDM) were diagnosed simultaneously is reported. Deposition of the kappa light chain in the cellular membrane of muscle fibers (observed with immunofluorescence techniques and ultrastructural examination) suggests a possible pathogenic mechanism for RDM.
报告了一例44岁男性患者,其同时被诊断为κ轻链多发性骨髓瘤和横纹肌溶解症(RDM)。κ轻链在肌纤维细胞膜中的沉积(通过免疫荧光技术和超微结构检查观察到)提示了RDM可能的致病机制。