Kövary P M, Niedorf H, Sommer G, Breu H, Kamanabroo P, Büchner T, Macher E
Dermatologica. 1977;154(3):138-46. doi: 10.1159/000251122.
We have observed non-myelomatous monoclonal hypergammaglobulinaemia in a 61-year-old man with Sézary syndrome. Similar cases have not been reported before. Sézary cells of patients studied by other investigators were found to be helper T cells. The abundant production of T-lymphocytic stimuli may possibly explain in our case the occurrence of a paraprotein.
我们在一名患有蕈样肉芽肿综合征的61岁男性患者中观察到非骨髓瘤性单克隆高丙种球蛋白血症。此前尚未有类似病例的报道。其他研究者研究的患者的蕈样肉芽肿细胞被发现是辅助性T细胞。在我们的病例中，T淋巴细胞刺激因子的大量产生可能解释了副蛋白的出现。
