Decaux O, Rodon P, Ruelland A, Estepa L, Leblay R, Grosbois B
Service de médecine interne, hôpital Sud, 16 boulevard de Bulgarie, BP 90347, 35203 Rennes cedex 02, France.
Rev Med Interne. 2007 Oct;28(10):670-6. doi: 10.1016/j.revmed.2007.04.011. Epub 2007 May 29.
Monoclonal gammopathy are common in the general population. We describe biological features and etiology of monoclonal gammopathy diagnosed during more than a ten year period in the Internal Medicine Department of Rennes University Hospital and in all the medical departments of General Hospital of Blois.
Patients were identified by immunofixation registry of Biochemistry Laboratories in both hospital (from 1990 in Rennes and from 1980 in Blois).
Internal Medicine Department of Rennes University Hospital: 1051 monoclonal gammapathies were identified: 514 men and 537 women. Median age was 71. Isotypes repartition was: IgG 42.8% (450 cases), IgM 31.9% (335), IgA 8.9% (94) biclonal gammopathy 9.8% (103). Sixty-nine monoclonal light chains (6.6%) were identified. Median concentration of monoclonal protein was 14 g/l (1.8-104.4). All department of General Hospital of Blois: 1282 monoclonal gammapathies were identified: 700 men and 582 women. Median age was 79. Isotypes repartition was: IgG 59.7% (765 cases), IgM 27.5% (329), IgA 11.8% (151). Thirty-four monoclonal light chains (2.7%) were identified. Median concentration of monoclonal protein was 5.6 g/l (0.5-96.6). Most frequent diagnosis were: monoclonal gammopathy of undetermined significance or MGUS (77.6% in Blois and 64.1% in Rennes), multiple myeloma (11.9% and 12.7%), Waldenström's macroglobulinemia (4.4% and 8.7%).
Monoclonal gammopathy are common in clinical practice. MGUS account for more than 60% of monoclonal gammopathy. Given their frequency, diagnostic and follow-up strategies must be costless and simple.
单克隆丙种球蛋白病在普通人群中很常见。我们描述了在雷恩大学医院内科以及布卢瓦综合医院所有科室超过十年期间诊断出的单克隆丙种球蛋白病的生物学特征和病因。
通过两家医院生物化学实验室的免疫固定登记来识别患者(雷恩从1990年开始,布卢瓦从1980年开始)。
雷恩大学医院内科:共识别出1051例单克隆丙种球蛋白病患者,其中男性514例,女性537例。中位年龄为71岁。免疫球蛋白类型分布为:IgG占42.8%(450例),IgM占31.9%(335例),IgA占8.9%(94例),双克隆丙种球蛋白病占9.8%(103例)。识别出69例单克隆轻链(6.6%)。单克隆蛋白的中位浓度为14g/l(1.8 - 104.4)。布卢瓦综合医院所有科室:共识别出1282例单克隆丙种球蛋白病患者,其中男性700例,女性582例。中位年龄为79岁。免疫球蛋白类型分布为:IgG占59.7%(765例),IgM占27.5%(329例),IgA占11.8%(151例)。识别出34例单克隆轻链(2.7%)。单克隆蛋白的中位浓度为5.6g/l(0.5 - 96.6)。最常见的诊断为:意义未明的单克隆丙种球蛋白病或MGUS(布卢瓦为77.6%,雷恩为64.1%)、多发性骨髓瘤(分别为11.9%和12.7%)、华氏巨球蛋白血症(分别为4.4%和8.7%)。
单克隆丙种球蛋白病在临床实践中很常见。MGUS占单克隆丙种球蛋白病的60%以上。鉴于其发病率,诊断和随访策略必须经济且简便。