Lolin Y I, Lam C W, Lo W H, Au K L, Masarei J R
Department of Chemical Pathology, Prince of Wales Hospital, Chinese University of Hong Kong, Shatin, NT.
J Clin Pathol. 1994 Jul;47(7):669-71. doi: 10.1136/jcp.47.7.669.
On initial presentation of a patient with IgD multiple myeloma there were no features to suggest an unusual variant. Two months later she developed spinal cord compression due to an IgD plasmacytoma. This complication of IgD myeloma has rarely been reported. During the course of the disease and using the routine laboratory protocol for investigating and identifying paraproteins, including IgD, the patient's results became indistinguishable from those in Bence-Jones proteinuria myeloma.
一名初诊为IgD型多发性骨髓瘤的患者,起初并无提示异常变异型的特征。两个月后,她因IgD型浆细胞瘤出现脊髓压迫。IgD型骨髓瘤的这一并发症鲜有报道。在疾病过程中,按照用于检测和鉴定副蛋白(包括IgD)的常规实验室方案,该患者的检测结果与本周氏蛋白尿骨髓瘤患者的结果难以区分。