Take H, Kubota K, Tamura K, Kurabayashi H, Shirakura T
Department of Medicine, Kusatsu Branch Hospital, Gunma University, School of Medicine, Japan.
J Med. 1996;27(3-4):228-32.
A 63-year-old Japanese male with a four-year history of asymptomatic hypogamma-globulinemia is presented. On admission, he had a mild bone marrow plasmacytosis at about 10% of the total nucleated cells, but had no anemia, no paraproteins nor bone lesions. Flow cytometric analysis showed a predominant proliferation of kappa chain-positive cells in the bone marrow and peripheral blood, and an increase in the proportion of natural killer cells in the peripheral blood. Furthermore, coexistent meningioma and transitional cell carcinoma of the bladder were subsequently found 9- and 15-months after the admission, respectively. We considered that a myeloma-induced, possible latent immunodeficiency may have allowed the additional tumor growth, and that this process may have been controlled by the cytotoxic subset of immune effector cells.
本文报告了一名63岁的日本男性,其患有无症状性低丙种球蛋白血症4年。入院时,他的骨髓浆细胞增多症较轻,约占总核细胞的10%,但无贫血、副蛋白血症或骨病变。流式细胞术分析显示骨髓和外周血中κ链阳性细胞显著增殖,外周血中自然杀伤细胞比例增加。此外,分别在入院后9个月和15个月发现并存的脑膜瘤和膀胱移行细胞癌。我们认为,骨髓瘤诱发的可能的潜在免疫缺陷可能促使了额外肿瘤的生长,而这一过程可能受到免疫效应细胞的细胞毒性亚群的控制。