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一名患有巨核细胞白血病和唐氏综合征儿童骨髓中的双着丝粒染色体。

Dicentric chromosome in the bone marrow of a child with megakaryoblastic leukaemia and Down's syndrome.

作者信息

Wilkie A O, Kitchen C, Oakhill A, Howell R T, Berry P J

机构信息

Department of Paediatric Oncology, Bristol Children's Hospital.

出版信息

J Clin Pathol. 1988 Apr;41(4):378-80. doi: 10.1136/jcp.41.4.378.

Abstract

A two year old girl with Down's syndrome (constitutional karyotype: 47 + 21), presenting with pancytopenia, developed acute megakaryoblastic leukaemia (AMKL). Her bone marrow contained an abnormal clone with a novel dicentric chromosome derived from chromosomes 5 and 7 (karyotype 46, XX, -5, -7, +dic (5;7) (p 13; p 11.2), +21. This case provides further evidence for a connection between chromosome 21 and this unusual form of childhood leukaemia, and raises questions about the loss of short arm material from chromosomes 5 and 7 compared with the more usual monosomy or long arm loss.

摘要

一名患有唐氏综合征(染色体核型为:47,XX,+21)的两岁女童,出现全血细胞减少,继而发展为急性巨核细胞白血病(AMKL)。她的骨髓中含有一个异常克隆,该克隆带有一条由5号和7号染色体衍生而来的新型双着丝粒染色体(染色体核型为46,XX,-5,-7,+dic(5;7)(p13;p11.2),+21)。该病例进一步证明了21号染色体与这种不寻常的儿童白血病形式之间存在关联,并引发了关于5号和7号染色体短臂物质缺失与更常见的单体性或长臂缺失相比的相关问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c592/1141459/4e0e2ba1f171/jclinpath00336-0018-a.jpg

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