Acute promyelocytic leukemia presenting initially with pancytopenia and severe hypocellular marrow which was successfully treated with all-trans retinoic acid and chemotherapy

Web Site オープンアクセス

この論文をさがす

抄録

A 62-year-old male developed pancytopenia due to severe hypocellular marrow. He was initially diagnosed with aplastic anemia (AA), and was treated with antilymphocyte globulin (ATG), cyclosporine (CyA), and granulocyte colonystimulating factor (G-CSF). However, 3 days after starting the therapy, the leukocyte count increased abruptly and the bone marrow became markedly hypercellular with hypergranulated promyelocytes. Cytogenetic analysis demonstrated t(15

収録刊行物

キーワード

詳細情報 詳細情報について

問題の指摘

ページトップへ