意义不明的单克隆伽玛病:为什么这些患者的鉴定和骨骼评估是重要的

James R. Berenson , Ori Yellin
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引用次数: 9

摘要

未确定意义单克隆γ病(MGUS)是一种浆细胞疾病,其特征是血清单克隆免疫球蛋白(m蛋白)含量≤3g /dL。它是一种无症状的恶性前病变,可发展为多发性骨髓瘤和相关的b细胞疾病。最近的研究表明,MGUS与骨质流失加剧和骨骼衰弱并发症有关,特别是椎体压缩性骨折(VCFs),通常导致背部疼痛。早期识别MGUS和评估骨状态将有助于用双膦酸盐进行预防性治疗,以增加骨密度,并可能降低骨折的风险,以及识别可能从早期手术干预中受益的vcf患者。通过适当的诊断和治疗策略,这些患者将体验到改善的结果和生活质量。
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Monoclonal Gammopathy of Undetermined Significance: Why Identification of These Patients and Assessment of Their Skeletons Is Important

Monoclonal gammopathy of undetermined significance (MGUS) is a plasma cell disorder characterized by the presence of a serum monoclonal immunoglobulin (M-protein) at ≤ 3 g/dL. It is an asymptomatic premalignant disorder that can progress to multiple myeloma and related B-cell disorders. Recent studies have suggested the association of MGUS with enhanced bone loss and debilitating skeletal complications, particularly vertebral compression fractures (VCFs) often leading to back pain. Early identification of MGUS and evaluation of bone status will facilitate prophylactic treatment with bisphosphonates to increase bone density and likely reduce the risk of fractures as well as identify patients with VCFs who might benefit from early surgical intervention. With proper diagnostic and treatment strategies, these patients will experience improved outcomes and quality of life.

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