Waldenström J G, Adner A, Gydell K, Zettervall O
Acta Med Scand. 1978;203(4):297-303. doi: 10.1111/j.0954-6820.1978.tb14877.x.
The combination of osteosclerosis, polyneuropathy, monoclonal immunoglobulin, hypertrichosis, serositis and a number of other symptoms is described. It seems probable that this is a special type of myeloma. Similar cases have been described in Japan and out findings are compared with the Japanese picture. The age of the patients is unusually low. The M-component in the plasma is small. There is very little Bence Jones protein in the urine and osteolytic lesions in the skull do not seem to have occurred. The polyneuropathy may improve during treatment with cytostatic drugs.
描述了骨硬化、多发性神经病、单克隆免疫球蛋白、多毛症、浆膜炎及许多其他症状的组合情况。这似乎可能是一种特殊类型的骨髓瘤。日本已描述过类似病例,并将我们的发现与日本的情况进行了比较。患者年龄异常低。血浆中的M成分较小。尿中本斯·琼斯蛋白极少,颅骨似乎未出现溶骨性病变。多发性神经病在用细胞毒性药物治疗期间可能会改善。