Mandahl N, Heim S, Kristoffersson U, Mitelman F, Rööser B, Rydholm A, Willén H
Hum Genet. 1985;71(4):321-4. doi: 10.1007/BF00388457.
In a malignant soft-tissue fibrous histiocytoma 50-56 chromosomes were found in the majority of the metaphases. The most frequent numerical aberrations were one or two extra copies of chromosomes 4, 5, 18, 20, 22, and a missing chromosome 15. Structural rearrangements encountered were 11p+ and 1-5 unidentifiable markers. The most conspicuous feature was pairs of chromosomes intimately associated or fused at their telomeres, observed in 20 out of 22 metaphases. Although the telomeres of 6p, 11p, 16q, 20q, and 21p were involved most frequently, no preferential pattern of associations was detectable. This peculiar chromosomal behavior is compared to similar observations recently reported in a case of a B-cell lymphoid leukemia.
在一例恶性软组织纤维组织细胞瘤中,多数中期相中发现有50 - 56条染色体。最常见的数目异常是染色体4、5、18、20、22多一条或两条拷贝,以及缺少一条染色体15。所遇到的结构重排为11p +和1 - 5个无法识别的标记。最显著的特征是在22个中期相中有20个观察到染色体对在其端粒处紧密相连或融合。虽然6p、11p、16q、20q和21p的端粒最常受累,但未检测到优先的关联模式。将这种特殊的染色体行为与最近报道的一例B细胞淋巴白血病病例中的类似观察结果进行了比较。