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Langerhans cell histiocytosis following acute leukemia in an adult

机译:成人急性白血病后朗格汉斯细胞组织细胞增生症

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To the editor: A 69-year-old man presents with cough and SOB approximatelyn3.5 years following diagnosis of a poorly differentiated acute lymphocyticnleukemia (progenitor cell phenotype). By flow cytometry, the initialnleukemia in 1998 was positive for HLA-DR, CD34, and CD45 and negativenfor lymphoid and myeloid markers including: CD3, CD5, CD7, CD19, CD10,nCD20, CD13, CD33, CD11b, and CD14; CD1a and S-100 protein stainingnwere not available on this sample. A pathologic diagnosis of a progenitorncell leukemia most suggestive of acute lymphocytic leukemia was made.nThe patient received induction therapy in November 1998 and achieved ancomplete remission. Consolidation therapy was discontinued after one cyclendue to severe cytopenias. Maintenance therapy was discontinued aftern6 months secondary to methotrexate-induced hepatoxicity.
机译:致编辑:一名69岁的男子在诊断出分化不良的急性淋巴细胞性白血病(祖细胞表型)后约3.5年出现咳嗽和SOB。通过流式细胞术,1998年的初始白血病为HLA-DR,CD34和CD45阳性,而淋巴样和髓样标记为阴性,包括:CD3,CD5,CD7,CD19,CD10,nCD20,CD13,CD33,CD11b和CD14;该样品没有CD1a和S-100蛋白染色。对该病进行了病理诊断,最能提示急性淋巴细胞白血病。n该患者于1998年11月接受了诱导治疗,并获得了完全缓解。一个周期后由于严重的血细胞减少症而中止合并治疗。甲氨蝶呤致肝毒性继发6个月后停止维持治疗。

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    《AMERICAN JOURNAL OF HEMATOLOGY》 |2009年第10期|p.1-10|共10页
  • 作者单位

    Clinical Fellow Hematology OncologyColumbia University Medical CenterConflicts of interest: Nothing to report.Published online 6 July 2009 in Wiley InterScience;

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