Mathew S, Head D, Rodriguez-Galindo C, Raimondi S C
Department of Pathology and Laboratory Medicine, St. Jude Children's Research Hospital, Memphis, TN 38105-2794, USA.
Leuk Lymphoma. 2000 Mar;37(1-2):213-8. doi: 10.3109/10428190009057648.
We report the clinical, hematologic, and cytogenetic findings for a child with secondary myelodysplastic syndrome (MDS) after treatment for a primitive neuroectodermal tumor. At the time of conversion to MDS, conventional cytogenetics revealed an unbalanced der(6)t(1;6) that resulted in trisomy of the long arm of chromosome 1 and partial monosomy and duplication of 6p. Using alpha satellite probes, fluorescence in situ hybridization of bone marrow cells showed that the rearranged chromosome contained the centromeres of both chromosomes 1 and 6, thus forming a dic(1;6) resulting in trisomy 1q. This report is the first to describe a case of childhood secondary myelodysplastic syndrome associated with a trisomy 1q involving chromosome 6.
我们报告了一名患有原始神经外胚层肿瘤并接受治疗后发生继发性骨髓增生异常综合征(MDS)儿童的临床、血液学和细胞遗传学检查结果。在转变为MDS时,传统细胞遗传学显示一条不平衡的der(6)t(1;6),导致1号染色体长臂三体以及6p部分单体和重复。使用α卫星探针,对骨髓细胞进行荧光原位杂交显示,重排的染色体包含1号和6号染色体的着丝粒,从而形成一个双着丝粒染色体dic(1;6),导致1q三体。本报告首次描述了一例与涉及6号染色体的1q三体相关的儿童继发性骨髓增生异常综合征病例。