Hashimoto Akari, Kanisawa Yuji, Fujimi Akihito, Nakajima Chisa, Hayasaka Naotaka, Yamada Shota, Okuda Toshinori, Minami Shinya, Yamauchi Natsumi, Iwasaki Sari, Suzuki Akira, Kato Junji
Department of Hematology and Oncology, Oji General Hospital, Japan.
Intern Med. 2016;55(6):683-7. doi: 10.2169/internalmedicine.55.5190. Epub 2016 Mar 15.
A 61-year-old woman with rheumatoid arthritis who was undergoing hemodialysis for end-stage renal failure was transferred to our hospital due to severe thrombocytopenia and anemia. A bone marrow biopsy showed the complete absence of megakaryocytes and erythroblasts. Cyclosporine treatment resulted in the improvement of her megakaryocyte and erythroblast levels, and a decrease in her serum level of anti-c-Mpl (thrombopoietin receptor) antibodies. After this initial improvement, her anemia progressively worsened, despite the continuous administration of immunosuppressive therapy with cyclosporine. Her platelet and leukocyte counts remained stable. This is the first report of a probable case of anti-c-Mpl antibody-associated pure red cell aplasia and acquired amegakaryocytic thrombocytopenic purpura.
一名61岁患有类风湿关节炎且因终末期肾衰竭正在接受血液透析的女性,因严重血小板减少症和贫血被转至我院。骨髓活检显示巨核细胞和幼红细胞完全缺失。环孢素治疗使她的巨核细胞和幼红细胞水平得到改善,血清抗c-Mpl(血小板生成素受体)抗体水平降低。在这一初步改善之后,尽管持续给予环孢素免疫抑制治疗,她的贫血仍逐渐加重。她的血小板和白细胞计数保持稳定。这是首例可能由抗c-Mpl抗体相关的纯红细胞再生障碍性贫血和获得性无巨核细胞性血小板减少性紫癜病例报告。