Mori Shunsuke, Ebihara Kenji
Clinical Research Center for Rheumatic Disease and Department of Rheumatology, Kumamoto Saishunsou National Hospital, 2659 Suya, Kohshi, Kumamoto, 861-1196, Japan.
Mod Rheumatol. 2008;18(6):634-8. doi: 10.1007/s10165-008-0106-4. Epub 2008 Jul 24.
Mizoribine has been recognized to have an acceptable toxicity profile compared with other immunosuppressants. In this study, however, we report a case of diabetic ketoacidosis and acute pancreatitis that suddenly occurred in a rheumatoid arthritis patient 2 weeks after introduction of mizoribine therapy. To the best of our knowledge, this is the first case in the literature to show mizoribine-induced diabetic ketoacidosis. Through prompt diagnosis and treatment, the patient recovered from these extremely rare but potentially lethal complications.
与其他免疫抑制剂相比,米唑立宾已被认为具有可接受的毒性特征。然而,在本研究中,我们报告了1例类风湿关节炎患者在开始米唑立宾治疗2周后突然发生糖尿病酮症酸中毒和急性胰腺炎的病例。据我们所知,这是文献中首例显示米唑立宾诱发糖尿病酮症酸中毒的病例。通过及时诊断和治疗,患者从这些极其罕见但可能致命的并发症中康复。