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[Frequent transformation to overt myelodysplastic syndrome in patients with aplastic anemia showing hematopoietic monoclonality at onset].

作者信息

Murai K, Numaoka H

出版信息

Rinsho Ketsueki. 2000 May;41(5):391-6.

PMID:10879097
Abstract
摘要

相似文献

1
[Frequent transformation to overt myelodysplastic syndrome in patients with aplastic anemia showing hematopoietic monoclonality at onset].
Rinsho Ketsueki. 2000 May;41(5):391-6.
2
Transformation of severe aplastic anemia into myelodysplastic syndrome with monosomy 7: monoclonal origin detected by HUMARA gene analysis during the aplastic anemia phase.伴有7号染色体单体的严重再生障碍性贫血转化为骨髓增生异常综合征：在再生障碍性贫血阶段通过HUMARA基因分析检测到单克隆起源
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3
[Hematological characteristics of hypoplastic MDS patients with chromosomal abnormalities, who had been followed for aplastic anemia with normal karyotypes].[染色体异常的低增生性骨髓增生异常综合征患者的血液学特征，这些患者曾因核型正常的再生障碍性贫血而接受随访]
Rinsho Ketsueki. 1997 Dec;38(12):1243-8.
4
Second allogeneic stem cell transplantation in a patient with hypoplastic myelodysplastic syndrome following a primary diagnosis of aplastic anaemia.再生障碍性贫血初诊后发生低增生性骨髓增生异常综合征患者的第二次异基因干细胞移植
Acta Haematol. 2011;125(3):175-8. doi: 10.1159/000322609. Epub 2010 Dec 30.
5
Therapy may unmask hypoplastic myelodysplastic syndrome that mimics aplastic anemia.治疗可能会揭示出类似再生障碍性贫血的低增生性骨髓增生异常综合征。
Cancer. 2007 Oct 1;110(7):1520-6. doi: 10.1002/cncr.22935.
6
Characterization of myelodysplastic syndrome and aplastic anemia by immunostaining of p53 and hemoglobin F and karyotype analysis: differential diagnosis between refractory anemia and aplastic anemia.通过p53和血红蛋白F免疫染色及核型分析对骨髓增生异常综合征和再生障碍性贫血进行特征描述：难治性贫血与再生障碍性贫血的鉴别诊断
Pathol Int. 2008 Jun;58(6):353-60. doi: 10.1111/j.1440-1827.2008.02236.x.
7
[Assessment of the bone marrow hematopoietic activity in aplastic anemia by point-counting method in relation to the clinical status and prognosis].
Rinsho Ketsueki. 1987 Jun;28(6):823-9.
8
Pluripotent hemopoietic precursors in vitro (CFUMIX) in aplastic anemia.
Exp Hematol. 1980 Oct;8(9):1165-71.
9
Primitive hematopoietic stem cells shows a polyclonal pattern in myelodysplastic syndromes.原始造血干细胞在骨髓增生异常综合征中呈现多克隆模式。
Haematologica. 2004 Jan;89(1):21-8.
10
Two cases showing clonal progression with full evolution from aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome to myelodysplastic syndromes and leukemia.两例显示克隆性进展，从再生障碍性贫血-阵发性睡眠性血红蛋白尿综合征完全演变为骨髓增生异常综合征和白血病。
Int J Hematol. 2000 Aug;72(2):206-9.