Bizzaro N, Pasini P
Istituto di Patologia Clinica, Ospedale Civile di S. Donà di Piave, Venezia, Italy.
Haematologica. 1990 Jan-Feb;75(1):58-63.
The etiology of monoclonal gammopathies remains unclear but familial occurrence of immunopathies seems to favor a possible hereditary background. In support of this view we report on a family in which five siblings had a monoclonal gammopathy. When MGUS was diagnosed in two of them, a family study was carried out: one sister died from multiple myeloma and four out of the seven living siblings were discovered to have a MGUS. The immunogenetic study (HLA) showed no direct correlation between haplotypes and the presence of the monoclonal protein. Nevertheless possible environmental exposure to viruses, chemicals and radiation was apparently excluded. This new report on familial involvement, the second ever reported for number of affected subjects, strongly supports the theory of genetic predisposition in the development of plasma cell dyscrasias.
单克隆丙种球蛋白病的病因尚不清楚,但免疫病的家族性发病似乎支持可能的遗传背景。为支持这一观点,我们报告了一个家庭,其中五个兄弟姐妹患有单克隆丙种球蛋白病。当其中两人被诊断为意义未明的单克隆丙种球蛋白血症(MGUS)时,开展了一项家族研究:一名姐妹死于多发性骨髓瘤,七名在世的兄弟姐妹中有四名被发现患有MGUS。免疫遗传学研究(HLA)显示单倍型与单克隆蛋白的存在之间无直接关联。然而,明显排除了可能的病毒、化学物质和辐射环境暴露。这份关于家族受累的新报告是有史以来第二篇报告受影响个体数量的报告,有力地支持了浆细胞发育异常中遗传易感性的理论。