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一例伴7号染色体单体性的先天性白血病。

A case of congenital leukemia with monosomy 7.

作者信息

Shitara T, Suetake N, Yugami S, Sotomatu M, Oshima Y, Ijima H, Kuroume T, Nakazawa S

机构信息

Department of Pediatrics, Gunma University School of Medicine, Japan.

出版信息

Ann Hematol. 1992 Dec;65(6):274-7. doi: 10.1007/BF01836073.

DOI:10.1007/BF01836073
PMID:1457590
Abstract

A case of congenital leukemia with monosomy 7 is reported. Immunological study of the blast cells using monoclonal antibodies was suggestive of both myelomegakaryocytic and T-lymphoblastic leukemia. Chromosomal analysis of the bone marrow cells showed monosomy 7. Chemotherapy was initiated with a combination of adriamycin, cytosine arabinoside, 6-mercaptopurine, and prednisolone. The patient obtained complete remission, which has been maintained for 4 years and 1 month. He receives no chemotherapy now. Our case shows that monosomy 7 in congenital leukemia is rare, but the presence of monosomy 7 in congenital leukemia does not necessarily indicate a poor prognosis.

摘要

报告了一例伴有7号染色体单体的先天性白血病病例。使用单克隆抗体对原始细胞进行的免疫学研究提示为骨髓巨核细胞性和T淋巴细胞母细胞性白血病。骨髓细胞的染色体分析显示7号染色体单体。采用阿霉素、阿糖胞苷、6-巯基嘌呤和泼尼松龙联合进行化疗。患者获得完全缓解,已维持4年1个月。他目前未接受化疗。我们的病例表明,先天性白血病中的7号染色体单体很少见,但先天性白血病中存在7号染色体单体并不一定预示预后不良。

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本文引用的文献

1
Leukemia in the newborn infant.新生儿白血病
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Congenital leukemia with monosomy 7.伴有7号染色体单体的先天性白血病。
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3
Cytogenetic findings in congenital leukemia: case report and review of the literature.先天性白血病的细胞遗传学发现:病例报告及文献综述
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Natural history of congenital leukemia. An experiment of nature revealing unexplored features of fetal-maternal isoimmunity, longest recorded survival following use of leukemostatic maternal isoantibody.先天性白血病的自然史。一项揭示胎儿-母体同种免疫未被探索特征的自然实验,使用抗白血病母体同种抗体后记录的最长生存期。
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Correlation of chromosome abnormalities with patient characteristics, histologic subtype, and induction success in children with acute nonlymphocytic leukemia.
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Spontaneous remission of presumed congenital acute nonlymphoblastic leukemia (ANLL) in a karyotypically normal neonate.一名核型正常的新生儿中推测的先天性急性非淋巴细胞白血病(ANLL)的自发缓解。
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Transient blueberry muffin appearance of a newborn with congenital monoblastic leukemia.
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Childhood myelodysplasia: suggested classification as myelodysplastic syndromes based on laboratory and clinical findings.儿童骨髓发育异常:基于实验室检查和临床发现建议将其分类为骨髓增生异常综合征
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