Schwartz H S, Jenkins R B, Dahl R J, Dewald G W
Cytogenetics Laboratory, Mayo Clinic, Rochester, MN 55905.
Clin Orthop Relat Res. 1989 Mar(240):250-60.
Giant-cell bone tumors are considered to be benign proliferations composed of poorly differentiated mononuclear cells and large multinucleated giant cells with the appearance of osteoclasts. Treatment is usually surgical resection, but there is a small risk of local recurrence and metastasis. Cytogenetic analyses were performed on giant-cell bone tumors of six consecutive patients. Chromosomally abnormal clones were found in three of the tumors, but no two patients had the same chromosome abnormality. Thus, there was no correlation between any specific chromosome change and the clinical behavior or histology of giant-cell bone tumors. However, all of the tumors had a significantly higher incidence of nonclonal chromosome abnormalities than is encountered in cultures of normal cells. The most common nonclonal abnormalities involved unusual telomere-to-telomere chromosome translocations. These findings suggest that the cells in these tumors are chromosomally unstable. The telomeres most frequently involved were on the long arm of chromosomes 19 and 20.
骨巨细胞瘤被认为是由分化不良的单核细胞和外观类似破骨细胞的大型多核巨细胞组成的良性增殖性病变。治疗通常采用手术切除,但存在局部复发和转移的小风险。对连续6例患者的骨巨细胞瘤进行了细胞遗传学分析。在其中3例肿瘤中发现了染色体异常克隆,但没有两名患者具有相同的染色体异常。因此,任何特定的染色体变化与骨巨细胞瘤的临床行为或组织学之间均无相关性。然而,所有肿瘤中非克隆性染色体异常的发生率均显著高于正常细胞培养中的发生率。最常见的非克隆性异常涉及不寻常的端粒到端粒的染色体易位。这些发现表明这些肿瘤中的细胞染色体不稳定。最常涉及的端粒位于19号和20号染色体的长臂上。