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实验室小单克隆异常的持续存在与临床进展。

Laboratory persistence and clinical progression of small monoclonal abnormalities.

机构信息

Division of Clinical Biochemistry and Immunology, Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA.

出版信息

Am J Clin Pathol. 2012 Oct;138(4):609-13. doi: 10.1309/AJCPT6OWWMHITA1Y.

Abstract

Monoclonal gammopathy of undetermined significance (MGUS) that presents with no quantifiable M spike on immunofixation electrophoresis (IFE) can be termed IFE MGUS. We retrospectively identified patients with IFE MGUS who were monitored with at least 1 subsequent assessment that included an IFE, and evaluated the persistence of the monoclonal protein and the progression of disease. Although the monoclonal proteins persisted in the majority of patients, 16% did not experience this persistence, and had no documented immunomodulatory therapy. After a median follow-up of 3.9 years, the disease clinically progressed in 14 patients (3.2%). Eight of these 14 patients with clinical progression had an immunoglobulin (Ig) A IFE M protein and 6 had an IgG M protein. This study demonstrates that in some patients with IFE MGUS, the M proteins are transient and that IgA IFE MGUS is more likely to persist and progress to myeloma.

摘要

意义未明的单克隆丙种球蛋白血症(MGUS),即在免疫固定电泳(IFE)上无可定量的 M 峰者,可称为 IFE-MGUS。我们回顾性地确定了具有 IFE-MGUS 的患者,这些患者至少进行了 1 次后续评估,包括 IFE,并评估了单克隆蛋白的持续存在和疾病的进展情况。尽管大多数患者的单克隆蛋白持续存在,但仍有 16%的患者未出现这种持续性,且未进行免疫调节治疗。中位随访 3.9 年后,14 例患者(3.2%)出现临床进展。在这 14 例临床进展的患者中,8 例有 IgA IFE M 蛋白,6 例有 IgG M 蛋白。本研究表明,在一些 IFE-MGUS 患者中,M 蛋白是一过性的,而 IgA IFE-MGUS 更可能持续存在并进展为骨髓瘤。

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Specificity of serum and urine protein electrophoresis for the diagnosis of monoclonal gammopathies.
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