Sreekantaiah C, Karakousis C P, Leong S P, Sandberg A A
Cancer Center of Southwest Biomedical Research, Institute and Genetrix, Inc., Scottsdale, Arizona 85251.
Cancer. 1992 May 15;69(10):2484-95. doi: 10.1002/1097-0142(19920515)69:10<2484::aid-cncr2820691017>3.0.co;2-2.
The cytogenetic findings in 31 liposarcomas from 26 patients are reported. Four other tumors did not grow. Three histologic types are represented in this analysis. The well-differentiated liposarcomas were characterized by telomeric associations, large marker chromosomes and ring chromosomes, and in some cases, double minutes. The pleomorphic liposarcomas contained very high clonal chromosomal numbers with near-tetraploid modes and numerous variable, often unidentifiable, chromosomal abnormalities. The myxoid liposarcomas were characterized primarily by a t(12;16)(q13;p11) as the sole abnormality or additional changes. These results indicate that cytogenetic findings may provide a new criterion, not only for establishing the diagnosis of liposarcoma, but also for differentiating confusing histologic types of liposarcoma and these lesions from other types of sarcomas.
报告了26例患者31例脂肪肉瘤的细胞遗传学结果。另外4个肿瘤未生长。本分析中有三种组织学类型。高分化脂肪肉瘤的特征是端粒联合、大的标记染色体和环状染色体,在某些情况下还有双微体。多形性脂肪肉瘤含有非常高的克隆染色体数,近四倍体模式以及许多可变的、通常无法识别的染色体异常。黏液样脂肪肉瘤主要特征是t(12;16)(q13;p11)作为唯一异常或其他改变。这些结果表明,细胞遗传学结果不仅可为脂肪肉瘤的诊断提供新标准,还可为区分脂肪肉瘤中令人困惑的组织学类型以及这些病变与其他类型肉瘤提供新标准。