Davison E V, Pearson A D, Emslie J, Reid M M, Malcolm A, Craft A W
Department of Human Genetics, University of Newcastle upon Tyne.
J Clin Pathol. 1989 Aug;42(8):797-9. doi: 10.1136/jcp.42.8.797.
A child with disseminated Ewing's sarcoma underwent cytogenetic investigations which showed different structural rearrangements of chromosome 22 at diagnosis (?ring22), and at relapse [t(10;22)], but the classic translocation t(11;22) was not detectable. This case provides further evidence of the importance of chromosome 22 in this disease, while raising some questions about the central importance of the translocation between chromosomes 11 and 22.
一名患有播散性尤因肉瘤的儿童接受了细胞遗传学检查,结果显示在诊断时(?22号环状染色体)以及复发时[t(10;22)] 22号染色体有不同的结构重排,但未检测到经典的t(11;22)易位。该病例进一步证明了22号染色体在这种疾病中的重要性,同时也对11号和22号染色体之间易位的核心重要性提出了一些疑问。