Orndal C, Mandahl N, Rydholm A, Nilbert M, Heim S, Akerman M, Mitelman F
Lund University Hospital, Department of Clinical Genetics, Sweden.
Acta Orthop Scand. 1990 Apr;61(2):99-105. doi: 10.3109/17453679009006497.
A myxoid liposarcoma showed macroscopic, histologic, and cytogenetic heterogeneity. In one of three myxoid nodules and in the surrounding lipoma-like tumor tissue, the translocation t(12;16)(q13;p11), known to be specific for myxoid liposarcoma, was found as the sole chromosomal abnormality. In the other two nodules, additional rearrangements involving chromosomes 1, 12, and 16 were found. These aberrations were probably secondary to the primary t(12;16), and are cytogenetic evidence of clonal evolution. The complex chromosome aberrations were present in those tumor parts that had more malignant histology, indicating that the acquisition of secondary chromosomal aberrations parallels the histologic manifestations of tumor progression.
黏液样脂肪肉瘤表现出宏观、组织学和细胞遗传学的异质性。在三个黏液样结节中的一个以及周围脂肪瘤样肿瘤组织中,发现已知对黏液样脂肪肉瘤具有特异性的易位t(12;16)(q13;p11)是唯一的染色体异常。在另外两个结节中,发现了涉及染色体1、12和16的其他重排。这些畸变可能继发于原发性t(12;16),是克隆进化的细胞遗传学证据。复杂的染色体畸变存在于那些具有更恶性组织学特征的肿瘤部分,表明继发性染色体畸变的获得与肿瘤进展的组织学表现平行。