Michlewitz H, Kawada C Y, Kennison R
J Reprod Med. 1985 Oct;30(10):781-3.
A postsplenectomy patient had idiopathic thrombocytopenic purpura (ITP) that was exacerbated with both her pregnancies. She failed to have sustained platelet counts in her previous pregnancy in spite of receiving steroids and chemotherapy. She underwent elective cesarean section with a platelet count of 7,000 but did not receive platelet transfusions. No unusual bleeding occurred, and an improvement in the ITP was noted postpartum.
一位脾切除术后患者患有特发性血小板减少性紫癜（ITP），在两次怀孕期间病情均加重。尽管她在之前的妊娠期间接受了类固醇和化疗，但血小板计数仍未能维持稳定。她在血小板计数为7000时接受了择期剖宫产手术，但未接受血小板输注。术后未发生异常出血情况，且产后ITP病情有所改善。
