Peltonen L, Nikoskelainen E, Kätkä K, Tyrkkö J
Dermatologica. 1984;169(4):207-10. doi: 10.1159/000249607.
A 42-year-old man had suffered from skin psoriasis for 27 years, psoriasis arthritis for 6 years and corneal crystalline deposits for 1 year, when an IgG-kappa monoclonal immunoglobulin was detected in his serum electrophoretic pattern. All the diagnostic studies for multiple myeloma were negative. However, 16 months later he developed this disease.
一名42岁男性患皮肤银屑病27年、银屑病关节炎6年、角膜晶体沉积1年,此时在其血清电泳图谱中检测到IgG-κ单克隆免疫球蛋白。所有针对多发性骨髓瘤的诊断研究均为阴性。然而,16个月后他患上了这种疾病。