Matsuno S, Tamaoka A, Yoshizawa K, Watanabe M, Shoji S
Department of Neurology, Institute of Clinical Medicine, University of Tsukuba, Ibaraki, Japan.
J Med. 2000;31(5-6):327-32.
The combination of idiopathic thrombocytopenic purpura (ITP) and myasthenia gravis (MG) has been reported infrequently. We report here the development of MG in a patient who underwent splenectomy for ITP ten years earlier, and describe the serum levels of anti-acetylcholine receptor antibodies (anti-AchR) and platelet-associated IgG (PAIgG) followed over 11 years. The concentrations of both autoantibodies have been decreased after thymectomy, suggesting that this procedure is potentially beneficial for treating both MG and ITP.
特发性血小板减少性紫癜(ITP)与重症肌无力(MG)并存的情况鲜有报道。我们在此报告1例10年前因ITP行脾切除术的患者发生MG的病例,并描述其11年来抗乙酰胆碱受体抗体(抗AchR)和血小板相关IgG(PAIgG)的血清水平。胸腺切除术后两种自身抗体浓度均下降,提示该手术可能对治疗MG和ITP均有益。