Lopez-Gines C, Cerda-Nicolas M, Kepes J, Donat J, Gil-Benso R, Llombart-Bosch A
Department of Pathology, Facultad de Medicina y Odontologia, Universidad de Valencia, Avda. Blasco Ibañez 17, 46010, Valencia, Spain.
Cancer Genet Cytogenet. 2000 Oct 15;122(2):149-52. doi: 10.1016/s0165-4608(00)00289-2.
Atypical teratoid/rhabdoid tumor of the central nervous system is a rare childhood tumor with a distinct histologic appearance and an aggressive clinical course. Few tumors have been analyzed cytogenetically. The only consistent chromosomal abnormality identified in some of these tumors has been monosomy or deletions of chromosome 22; in others, a normal chromosome 22 was present. The authors report an atypical teratoid/rhabdoid neoplasm of the central nervous system with a novel complex rearrangement affecting chromosomes 6 and 11 as the sole anomaly. The involvement of region 11p15 could be important in the pathogenesis of this entity.
中枢神经系统非典型畸胎样/横纹肌样肿瘤是一种罕见的儿童肿瘤,具有独特的组织学表现和侵袭性临床病程。很少有肿瘤进行过细胞遗传学分析。在其中一些肿瘤中唯一一致鉴定出的染色体异常是22号染色体单体或缺失;在其他肿瘤中,22号染色体正常。作者报告了一例中枢神经系统非典型畸胎样/横纹肌样肿瘤,其具有影响6号和11号染色体的新型复杂重排,这是唯一的异常。11p15区域的受累在该实体的发病机制中可能很重要。