Dash S, Punnose J, Dash R J
Jpn J Med. 1986 Feb;25(1):57-8. doi: 10.2169/internalmedicine1962.25.57.
A rare instance of IgG-kappa monoclonal gammopathy in a patient with beta-thalassaemia trait is reported. The patient had a smoldering multiple myeloma with no apparent clinical symptoms pertaining to the disease and was a non-responder to conventional Melphalan and prednisolone therapy. Beta-thalassaemia trait was detected while investigating him for anaemia. A state of altered immunological reactivity, chronic infections and associated biliary tract disease are some of the pathogenetic mechanisms suggested. However in this patient none of these were operative.
报告了一例β地中海贫血特征患者中罕见的IgG-κ单克隆丙种球蛋白病病例。该患者患有冒烟型多发性骨髓瘤,无明显与该疾病相关的临床症状,并且对传统的美法仑和泼尼松龙治疗无反应。在对其贫血进行调查时检测到β地中海贫血特征。有人提出免疫反应性改变、慢性感染和相关胆道疾病等是一些致病机制。然而,在该患者中这些机制均未起作用。