Milatovich A, Heerema N A, Palmer C G
Department of Medical Genetics, Indiana University School of Medicine, Indianapolis.
Cancer Genet Cytogenet. 1990 May;46(1):41-53. doi: 10.1016/0165-4608(90)90007-w.
Thirty cases of endometrial malignancy were successfully studied cytogenetically. Twenty-four of the cases were endometrial adenocarcinomas. Twenty-three of these were stage I tumors, and the twenty-fourth was a stage IV tumor. Fourteen of the stage I adenocarcinomas had abnormal chromosomes, and nine had apparently normal chromosomes. No two tumors had an identical chromosomal rearrangement. Trisomy 1q was common however; 10 of the 14 tumors with abnormal chromosomes had a chromosome 1 abnormality. Clinical and pathologic data were available for 17 of these patients. There appeared to be no relationship between prognostic indicators and the tumor karyotype except for uterine size. Six cases of endometrial malignant mixed müllerian tumor (MMMT) of the homologous type were also analyzed cytogenetically. Three of these tumors had very abnormal karyotypes, and the remaining three had apparently normal chromosomes. Structural abnormalities of chromosome 1, 3, and 5 were present in all three tumors with abnormal karyotypes, but identical breakpoints or rearrangements were not observed.
对30例子宫内膜恶性肿瘤患者成功进行了细胞遗传学研究。其中24例为子宫内膜腺癌。这些病例中有23例为I期肿瘤,第24例为IV期肿瘤。I期腺癌中有14例染色体异常,9例染色体明显正常。没有两个肿瘤具有相同的染色体重排。然而,1号染色体三体很常见;14例染色体异常的肿瘤中有10例存在1号染色体异常。17例患者有临床和病理数据。除子宫大小外,预后指标与肿瘤核型之间似乎没有关系。还对6例同源型子宫内膜恶性苗勒管混合瘤(MMMT)进行了细胞遗传学分析。其中3例肿瘤核型非常异常,其余3例染色体明显正常。所有3例核型异常的肿瘤均存在1号、3号和5号染色体结构异常,但未观察到相同的断点或重排。