Berner Y, Berrebi A
Isr J Med Sci. 1986 Feb;22(2):109-12.
Five patients with myeloproliferative disorders and paraprotein are reported. The diseases included acute myelomonocytic leukemia, chronic myeloid leukemia, sideroblastic anemia with excess of blasts, polycythemia vera and myelofibrosis. In four cases, the paraprotein was of the IgG k type and in one, IgM k. No evidence of multiple myeloma or excessive plasmacytosis was noted. The literature records 19 other myeloid disorders with this unusual association. Although the pathogenesis remains unclear, three possible explanations are suggested: disturbance of the pluripotent stem cell resulting in a combined myeloplasmatic disorder, coexistence of two diseases, or a fortuitous association.
报告了5例患有骨髓增殖性疾病和副蛋白血症的患者。这些疾病包括急性粒单核细胞白血病、慢性粒细胞白血病、伴有原始细胞增多的铁粒幼细胞贫血、真性红细胞增多症和骨髓纤维化。4例患者的副蛋白为IgG κ型,1例为IgM κ型。未发现多发性骨髓瘤或浆细胞增多的证据。文献记载了另外19例伴有这种不寻常关联的髓系疾病。尽管发病机制尚不清楚,但提出了三种可能的解释:多能干细胞紊乱导致髓质联合性疾病、两种疾病并存或偶然关联。