Tzeng C C, Cheng J Y, Lin J C, Meng C L
Department of Pathology, National Cheng Kung University Medical Center, Tainan, R.O.C.
Zhonghua Yi Xue Za Zhi (Taipei). 1992 Aug;50(2):96-102.
Seven cases of primary rectosigmoid epithelial neoplasm, including a tubular adenoma, a villous adenoma with malignant change and five adenocarcinomas, were cytogenetically studied with short-term cultivation and GTG-banding. The tubular adenoma showed karyotypic normality. The other six malignant tumors were hyperdiploid in chromosomal modal number and showed multiple aberrations. The complexity of chromosomal aberrations increased proportionally to the pathologic stage. No common chromosome change to all of the tumors was found. The most common recurrent chromosome changes were extra gains of chromosomes #7 and #8q, which were found respectively in four of the six malignant tumors. Two recurrent structurally abnormal chromosomes were i(8q) and der(10)t(10;?)(p15;?). No case showed sex chromosome change, except one tumor from a male patient who obtained an extra X chromosome. All these chromosome changes found were consistent with the results reported by other investigators. Deletions of #5q and #17 were nevertheless only found in one and two of our six malignant cases, respectively. No cases showed a deletion of #18q. The possible molecular mechanisms of these recurrent chromosome aberrations were also discussed.
对7例原发性直肠乙状结肠上皮肿瘤进行了细胞遗传学研究,包括1例管状腺瘤、1例伴有恶变的绒毛状腺瘤和5例腺癌,采用短期培养和GTG显带技术。管状腺瘤核型正常。其他6例恶性肿瘤染色体众数为超二倍体,且有多个畸变。染色体畸变的复杂性与病理分期成比例增加。未发现所有肿瘤共有的染色体改变。最常见的重复性染色体改变是分别在6例恶性肿瘤中的4例中发现的额外的7号染色体和8q染色体增加。两个重复性结构异常染色体是i(8q)和der(10)t(10;?)(p15;?)。除1例男性患者的肿瘤获得一条额外的X染色体外,未发现有性染色体改变的病例。所有这些发现的染色体改变与其他研究者报道的结果一致。然而,5q和17号染色体的缺失分别仅在我们6例恶性病例中的1例和2例中发现。未发现有18q缺失的病例。还讨论了这些重复性染色体畸变可能的分子机制。