Merlo C, Wimpfheimer C, Muser J, Keller U
Medizinische Klinik, Kantonsspital Luzern.
Schweiz Med Wochenschr. 1992 Oct 24;122(43):1622-6.
We report the case of a 78-year-old patient with recurrent attacks of severe fasting and late postprandial hypoglycemia, whose plasma showed highly elevated concentrations of immunoreactive insulin evidenced by high titers of spontaneous insulin and proinsulin-binding antibodies. Insulin autoimmune syndrome was diagnosed. Further investigations revealed a multiple myeloma of the kappa-light chain type. The monoclonal insulin-binding antibodies were characterized as IgG2-subclass and were identical with the paraprotein, thereby confirming that the insulin-binding antibodies were in fact produced by the myeloma. Together with initial symptomatic treatment, plasmapheresis was performed repeatedly to reduce the antibody pool. Subsequently octreotide therapy proved successful. The underlying myeloma was treated by chemotherapy.
我们报告了一例78岁患者,其出现严重空腹及餐后晚期低血糖反复发作,血浆显示免疫反应性胰岛素浓度大幅升高,高滴度的自发性胰岛素和胰岛素原结合抗体可证明这一点。诊断为胰岛素自身免疫综合征。进一步检查发现为κ轻链型多发性骨髓瘤。单克隆胰岛素结合抗体被鉴定为IgG2亚类,且与副蛋白相同,从而证实胰岛素结合抗体实际上是由骨髓瘤产生的。除了初始对症治疗外,反复进行血浆置换以减少抗体池。随后,奥曲肽治疗证明是成功的。潜在的骨髓瘤通过化疗进行治疗。