Obayashi H, Kanoh T, Shimazaki C, Horiike S, Nakamura M, Fukui I
Department of Clinical Research, Kyoto Microbiological Institute.
Rinsho Byori. 1991 Jun;39(6):661-5.
By a combined use of immunoelectrophoresis and immunofixation, we detected 13 cases of double gammopathy among 269 cases of monoclonal gammopathy investigated between 1986 and 1990. The incidence of double gammopathy (4.8%) was greater than that in previous studies. Double gammopathy was classified into 5 groups: (1) identical pairs of both heavy (H)- and light (L)-chains (1 case); (2) identical H-chains and different L-chains (2 cases); (3) different H-chains and identical L-chains (3 cases); (4) different pairs of both H- and L-chains (5 cases); and (5) monoclonal immunoglobulin and Bence Jones protein of different type (2 cases). An additional M-component was detected during the course of illness in 2 of the 13 cases. As to H-chain combinations, a pair of IgG and IgA (46%) was most frequently encountered. Seven patients had myeloma, three benign double gammopathy and two macroglobulinemia. One case of benign double gammopathy developed IgA (lambda) myeloma three years after the diagnosis. Serum and urine immunofixation is a useful method to detect a trace amount of M-component and to follow up the clinical course of monoclonal gammopathy.
通过联合使用免疫电泳和免疫固定法,我们在1986年至1990年期间调查的269例单克隆丙种球蛋白病患者中检测到13例双克隆丙种球蛋白病。双克隆丙种球蛋白病的发病率(4.8%)高于以往研究。双克隆丙种球蛋白病分为5组:(1)重链(H)和轻链(L)均相同的配对(1例);(2)H链相同而L链不同(2例);(3)H链不同而L链相同(3例);(4)H链和L链均不同的配对(5例);(5)不同类型的单克隆免疫球蛋白和本周蛋白(2例)。13例患者中有2例在病程中检测到额外的M蛋白成分。至于H链组合,最常见的是一对IgG和IgA(46%)。7例患者患有骨髓瘤,3例为良性双克隆丙种球蛋白病,2例为巨球蛋白血症。1例良性双克隆丙种球蛋白病患者在诊断后3年发展为IgA(λ)骨髓瘤。血清和尿液免疫固定法是检测微量M蛋白成分和随访单克隆丙种球蛋白病临床病程的有用方法。