Chen W J, Eng H L, Fang F M
Department of Pathology, Chang Gung Memorial Hospital, Kaohsiung, Taiwan, R.O.C.
Chang Gung Med J. 2000 Sep;23(9):520-8.
Mesenchymal neoplasms of the gastrointestinal tract remain controversial in regard to both diagnostic criteria and prognostic factors. In order to investigate whether DNA ploidy in a single area of a tumor can be representative of the entire tumor, multiple samples from the same tumor were analyzed in 79 cases of gastrointestinal stromal tumors.
Forty-three male and 36 female patients, aged 11 to 80 years with stromal tumors of the GI tract were selected. Flow cytometric DNA ploidy analysis was done on tissue cut from paraffin blocks by using the modified technique of Hedley et al.
All 34 benign stromal tumors displayed a concordant diploid DNA content. Eighteen (40%) of the 45 malignant stromal tumors (13 low-grade, 5 high-grade) were diploid. Aneuploid and polyploid DNA stemlines were found in 10 cases (43.4%) of low-grade stromal tumors, and in 17 cases (77.2%) of high-grade stromal tumors. DNA polyploidy was identified in 21 (46.7%) of 45 malignant stromal tumors. Also, aneuploid populations were accompanied by diploid populations.
DNA content correlated well with histologic category. Tumor aneuploidy was more frequently seen in tumors of advanced stage, but no relationship was seen between tumor stage and the presence of tumor heterogeneity. Differences in ploidy levels were thus not necessarily associated with apparent differences in histologic patterns. The mechanism responsible for regional differences in DNA ploidy in the same tumor remain unexplained. Several hypotheses are reviewed.
胃肠道间叶肿瘤在诊断标准和预后因素方面仍存在争议。为了研究肿瘤单个区域的DNA倍性是否能代表整个肿瘤,对79例胃肠道间质瘤的同一肿瘤的多个样本进行了分析。
选取43例男性和36例女性患者,年龄在11至80岁之间,患有胃肠道间质瘤。采用Hedley等人的改良技术对石蜡块切取的组织进行流式细胞术DNA倍性分析。
所有34例良性间质瘤均显示一致的二倍体DNA含量。45例恶性间质瘤(13例低级别、5例高级别)中有18例(40%)为二倍体。在10例(43.4%)低级别间质瘤和17例(77.2%)高级别间质瘤中发现了非整倍体和多倍体DNA干系。45例恶性间质瘤中有21例(46.7%)鉴定为DNA多倍体。此外,非整倍体群体伴有二倍体群体。
DNA含量与组织学类别密切相关。肿瘤非整倍体在晚期肿瘤中更常见,但未发现肿瘤分期与肿瘤异质性之间的关系。因此,倍性水平的差异不一定与组织学模式的明显差异相关。同一肿瘤中DNA倍性区域差异的机制仍未得到解释。本文对几种假说进行了综述。