Wille L E, Ostborg J
Acta Med Scand. 1979;205(3):243-5. doi: 10.1111/j.0954-6820.1979.tb06038.x.
A well established case of von Recklinghausen's neurofibromatosis, in which a biclonal gammopathy developed, has been studied. One of the paraproteins was characterized as IgG kappa, the other as IgG lambda. This combination of anomalies has not been described previously in the literature.
对一例确诊的冯雷克林霍增氏神经纤维瘤病患者进行了研究，该患者出现了双克隆丙种球蛋白病。其中一种副蛋白被鉴定为IgG κ，另一种为IgG λ。这种异常组合在以往文献中尚未见报道。
