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与造血系统恶性肿瘤中多谱系造血祖细胞相关的染色体异常inv(3)(q21q26)

Chromosomal abnormality inv(3)(q21q26) associated with multilineage hematopoietic progenitor cells in hematopoietic malignancies.

作者信息

Shi G, Weh H J, Dührsen U, Zeller W, Hossfeld D K

机构信息

Department of Oncology/Hematology, University Hospital Eppendorf, University of Hamburg, Germany.

出版信息

Cancer Genet Cytogenet. 1997 Jul 1;96(1):58-63. doi: 10.1016/s0165-4608(96)00293-2.

Abstract

We have identified ten patients with acute myeloid leukemia (AML) and one patient with chronic myeloid leukemia with megakaryocytic crisis who displayed an inv(3)(q21q26). Seven of them had an additional monosomy 7. Most of them had a myelodysplastic syndrome (MDS) preceding AML, normal or increased platelet counts, increased number of megakaryocyte, megakaryocytic dysplasia, and erythroid dysplasia. There was a high incidence of resistance to induction chemotherapy, short remission time, and early relapse. Seven patients were immunologically analyzed. The main immunophenotypes were as follow: CD7+, CD34+, HLA-DR+, CD38+, CD13+, CD33+, CDw65+, CD2-, CD3-, CD4-, CD8-, CD19+, CD20-, CD11b-. Our results suggest that the leukemia with inv(3)(q21q26) represents a new cytogenetic-clinicopathologic subtype, characterized by 1) abnormal megakaryopoiesis and multiple hematopoietic lineage involvement; 2) an antecedent MDS; 3) poor response to conventional chemotherapy; and 4) expression of CD7, CD34, CD38, HLA-DR, CD13, and CD33 antigens. We propose that the malignant transformation in patients with inv(3)(q21q26) occurs in an early stem cell prior to lineage commitment.

摘要

我们已鉴定出10例急性髓系白血病(AML)患者和1例慢性髓系白血病伴巨核细胞危象患者,他们均表现出inv(3)(q21q26)。其中7例还伴有额外的7号染色体单体。他们中的大多数在AML之前患有骨髓增生异常综合征(MDS),血小板计数正常或增加,巨核细胞数量增加,存在巨核细胞发育异常和红系发育异常。诱导化疗耐药的发生率高,缓解期短且早期复发。对7例患者进行了免疫分析。主要免疫表型如下:CD7+、CD34+、HLA-DR+、CD38+、CD13+、CD33+、CDw65+、CD2-、CD3-、CD4-、CD8-、CD19+、CD20-、CD11b-。我们的结果表明,伴有inv(3)(q21q26)的白血病代表一种新的细胞遗传学 - 临床病理亚型,其特征为:1)异常巨核细胞生成和多造血谱系受累;2)前驱MDS;3)对传统化疗反应不佳;4)CD7、CD34、CD38、HLA-DR、CD13和CD33抗原的表达。我们提出,伴有inv(3)(q21q26)的患者的恶性转化发生在谱系定向之前的早期干细胞中。

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