Fine J M, Muller J Y, Rochu D, Marneux M, Gorin N C, Fine A, Lambin P
Acta Med Scand. 1986;220(4):369-73. doi: 10.1111/j.0954-6820.1986.tb02780.x.
This paper reports a unique familial occurrence of Waldenström's macroglobulinemia (WM) in monozygotic twins. The determination of twin monozygosity has been performed by electrophoretic and immunological typing of genetic systems (erythrocyte blood groups, leucocyte antigens and serum protein polymorphism). The two monoclonal IgM differ one from the other by their light chain type and their idiotypic determinants. Although a genetic predisposition to WM exists in these twins, the gene recombination leading to idiotypic specificity and light chain assortment occurs independently of the monoclonal malignant involvement.
本文报道了单卵双胞胎中独特的家族性瓦尔登斯特伦巨球蛋白血症(WM)病例。通过对遗传系统(红细胞血型、白细胞抗原和血清蛋白多态性)进行电泳和免疫分型来确定双胞胎的单合子性。这两种单克隆IgM在轻链类型和独特型决定簇方面彼此不同。尽管这些双胞胎存在WM的遗传易感性,但导致独特型特异性和轻链分类的基因重组独立于单克隆恶性病变发生。