Fine J M, Lambin P, Muller J Y
Acta Med Scand. 1979;205(4):339-41.
Twenty cases of "asymptomatic" monoclonal gammopathies were detected by routine electrophoresis in patient's sera or in blood donors and were followed over 3-14 years. Four cases have shown a malignant evolution-two evolved toward Waldenström's macroglobulinemia after 3 years and two could be classified as myeloma 3 and 7 years, respectively, after detection of the monoclonal protein. The remaining cases were still "asymptomatic" 4 years later (7 cases), 7-9 years later (8 cases) and 14 years later (1 case). A malignant evolution occurred in approximately 20% of cases.
通过对患者血清或献血者血清进行常规电泳,检测出20例“无症状”单克隆丙种球蛋白病,并对其进行了3至14年的随访。4例出现了恶性进展——2例在3年后演变为华氏巨球蛋白血症,另外2例在检测到单克隆蛋白后分别于3年和7年被归类为骨髓瘤。其余病例在4年后(7例)、7至9年后(8例)和14年后(1例)仍“无症状”。约20%的病例出现了恶性进展。