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[粒细胞集落刺激因子和促红细胞生成素治疗后再生障碍性贫血转化为急性髓系白血病伴骨髓纤维化]

[Transformation of aplastic anemia to acute myeloid leukemia with myelofibrosis following treatment with granulocyte colony-stimulating factor and erythropoietin].

作者信息

Tsurumi H, Yamada T, Hara T, Murakami N, Moriwaki H, Muto Y

机构信息

First Department of Internal Medicine, Gifu University School of Medicine.

出版信息

Rinsho Ketsueki. 1996 Jul;37(7):630-2.

PMID:8779784
Abstract

A 67-year-old female was admitted with fatigue. Peripheral blood examination showed severe pancytopenia. Bone marrow biopsy revealed hypoplastic marrow. She was diagnosed as having aplastic anemia. Steroid pulse therapy was not effective. After treatment with erythropoietin (EPO) and granulocyte colony-stimulating factor (G-CSF), blasts which were positive for CD13, CD33, CD34 and HLA-DR and negative for myeloperoxidase appeared in the peripheral blood. At this time, bone marrow biopsy revealed myelofibrosis with increased blasts. Chromosome analysis showed 46XX, add (1) (p36), add (1) (q44), -2, -5, del (7) (q11), -12, +3mar. She died of pneumonia despite chemotherapy with etoposide. Administration of EPO and G-CSF may have led to the rapid development of leukemia and myelofibrosis.

摘要

一名67岁女性因疲劳入院。外周血检查显示严重全血细胞减少。骨髓活检显示骨髓增生低下。她被诊断为再生障碍性贫血。类固醇冲击疗法无效。在用促红细胞生成素(EPO)和粒细胞集落刺激因子(G-CSF)治疗后,外周血中出现了CD13、CD33、CD34和HLA-DR阳性、髓过氧化物酶阴性的原始细胞。此时,骨髓活检显示伴有原始细胞增多的骨髓纤维化。染色体分析显示46XX,add(1)(p36),add(1)(q44),-2,-5,del(7)(q11),-12,+3mar。尽管接受了依托泊苷化疗,她仍死于肺炎。EPO和G-CSF的使用可能导致了白血病和骨髓纤维化的快速发展。

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