[意义不明的单克隆γ病]。

P. Chaïbi, L. Merlin, C. Thomas, F. Piette
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引用次数: 5

摘要

未确定意义单克隆伽玛病(MGUS)是一种血清单克隆免疫球蛋白低于30 g/l的无症状疾病。它优先影响老年患者;MGUS患病率在一般人群中约为1%,在80岁以上患者中约为10%。MGUS的诊断是基于消除其他原因的血清单克隆免疫球蛋白,特别是多发性骨髓瘤。在MGUS诊断后的20年内,约25%的患者会发展为骨髓瘤或其他恶性淋巴细胞增生性疾病。到目前为止,还没有发现任何因素可以有效地预测这种演变。最近关于浆细胞免疫表型、细胞遗传学和分子生物学的数据表明MGUS与多发性骨髓瘤之间存在联系。MGUS现在清楚地表现为恶性程度降低的浆细胞单克隆病理。不久,新的生物学数据将有助于区分终身无症状的MGUS患者和那些将发展为恶性淋巴细胞增生性疾病的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Monoclonal gammopathy of undetermined significance].
Monoclonal gammopathy of undetermined significance (MGUS) is an asymptomatic disorder with serum monoclonal immunoglobulin less than 30 g/l. It preferentially affects elderly patients; MGUS prevalence is about 1% in the general population and about 10% in patients aged over 80 years. MGUS diagnosis is based on elimination of other causes of serum monoclonal immunoglobulin, particularly multiple myeloma. Within the 20 years following diagnosis of MGUS, about 25% of patients will evolve towards myeloma or other malignant lymphoproliferative disorder. No factor has been identified to date which can efficiently predict this evolution. Recent data concerning immunophenotype, cytogenetics and molecular biology of plasma cells demonstrate the link between MGUS and multiple myeloma. MGUS clearly appears now as a plasma cell monoclonal pathology with reduced malignity. Soon, new biological data would help to discriminate patients with MGUS who will remain asymptomatic life-long from those who will evolve towards malignant lymphoproliferative disorder.
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