Bown N P, Reid M M, Malcolm A J, Davison E V, Craft A W, Pearson A D
Department of Human Genetics, University of Newcastle upon Tyne, United Kingdom.
Med Pediatr Oncol. 1994;23(2):124-9. doi: 10.1002/mpo.2950230210.
Between 1987 and 1991, cytogenetic studies were carried out on small round cell tumours of 68 patients from the Northern Health Region of England. Clonal chromosome abnormalities were found in 30, comprising 15 neuroblastomas, 7 Ewing's tumours, 7 rhabdomyosarcomas, and 1 granular cell tumour. Characteristic rearrangements were found in five cases of Ewing's tumour [all with translocation t(11;22) (q24;q12)] and in four cases of rhabdomyosarcoma [all with evidence of translocation t(2;13) (q35-37;q14)]. In one case of Ewing's tumour and three of rhabdomyosarcoma, the cytogenetic findings were important in diagnosis. Within the neuroblastomas, examples were found of hyperdiploidy, 1p rearrangements, double minute chromosomes, and homogeneously staining regions, but too few cases were available for prognostic associations to be assessed. Our findings confirm the diagnostic importance of chromosome abnormalities in small round cell tumours and indicate that cytogenetic analysis should be an intrinsic part of the initial investigations of all patients with such tumours.
1987年至1991年间,对英格兰北部健康地区68例小细胞肿瘤患者进行了细胞遗传学研究。在30例患者中发现了克隆性染色体异常,其中包括15例神经母细胞瘤、7例尤因肉瘤、7例横纹肌肉瘤和1例颗粒细胞瘤。在5例尤因肉瘤病例中发现了特征性重排[均伴有t(11;22)(q24;q12)易位],在4例横纹肌肉瘤病例中发现了特征性重排[均有t(2;13)(q35 - 37;q14)易位的证据]。在1例尤因肉瘤和3例横纹肌肉瘤病例中,细胞遗传学结果对诊断具有重要意义。在神经母细胞瘤中,发现了超二倍体、1p重排、双微体染色体和均匀染色区的例子,但由于病例数量太少,无法评估其预后相关性。我们的研究结果证实了染色体异常在小细胞肿瘤诊断中的重要性,并表明细胞遗传学分析应成为所有此类肿瘤患者初始检查的固有组成部分。