Anderson M J, Woods V L, Tani P, Lindstrom J M, Schmidt D, McMillan R
Ann Intern Med. 1984 Jun;100(6):829-31. doi: 10.7326/0003-4819-100-6-829.
The coexistence of chronic idiopathic thrombocytopenic purpura and myasthenia gravis has been infrequently reported. We report another case and show the coexistence of autoantibodies to the platelet glycoprotein IIb and IIIa complex and the acetylcholine receptor. Autoantibody levels were followed during 8 weeks of treatment with cyclophosphamide, vincristine, and prednisone; the concentration of both autoantibodies fell during treatment but without measureable clinical improvement.
慢性特发性血小板减少性紫癜与重症肌无力并存的情况鲜有报道。我们报告了另一例病例,并展示了血小板糖蛋白IIb和IIIa复合物自身抗体与乙酰胆碱受体自身抗体的并存。在使用环磷酰胺、长春新碱和泼尼松治疗的8周期间,对自身抗体水平进行了跟踪;两种自身抗体的浓度在治疗期间均有所下降,但未观察到可测量的临床改善。