孙靖驰,许在华,王 振.染色体1p、19q缺失检测在胶质瘤病理诊断中的意义[J].肿瘤学杂志,2018,24(10):973-976. |
染色体1p、19q缺失检测在胶质瘤病理诊断中的意义 |
Detection of Chromosome 1p and 19q Deletions in Pathological Diagnosis of Glioma Types |
投稿时间:2017-12-14 |
DOI:10.11735/j.issn.1671-170X.2018.10.B007 |
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中文关键词: 1p 19q 共缺失 杂合性缺失 胶质瘤 |
英文关键词:1p 19q co-deletion loss of heterozygosity glioma |
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中文摘要: |
摘 要:[目的] 研究染色体1p和19q的缺失在不同病理类型胶质瘤中的分布差异,评价其在胶质瘤病理鉴别诊断中的价值。[方法] 选取经术后病理确诊的Ⅱ~Ⅲ级胶质瘤患者共134例。采用特异性扩增片段分析法检测肿瘤组织染色体1p、19q缺失情况。[结果] 134例患者中,组织病理学认定为间变性少突胶质细胞瘤(anaplastic oligodendroglioma,AO,WHO Ⅲ级)9例(6.7%),少突胶质细胞瘤(oligodendroglial tumor,OT,WHO Ⅱ级)15例(11.2%),混合型胶质瘤(星形+少突)32例(23.9%),星型细胞瘤(astrocytoma,AA)78例(58.2%)。少突胶质细胞瘤、间变性少突胶质细胞瘤、混合型胶质瘤、星型细胞瘤的1p、19q缺失率为分别为73.3%(11/15)和 66.7%(10/15)、 66.7%(6/9)和77.8%(7/9)、53.1%(17/32)和59.4%(19/32)、43.6%(34/78)和41.0%(32/78)。染色体1p和19q的缺失情况(包括完整,杂合性缺失,联合缺失)在少突胶质细胞瘤、混合型胶质瘤、星型细胞瘤的分布差异有统计学意义(P<0.05),但在不同级别少突胶质细胞瘤中,染色体缺失差异无统计学意义。 [结论] 染色体1p、19q的缺失与胶质瘤病理类型相关。单纯依靠组织病理学诊断难以准确判断胶质瘤类型,检测染色体1p、19q缺失情况可作为胶质瘤病理诊断的重要参考指标。 |
英文摘要: |
Abstract:[Objective] To evaluate the chromosome 1p and 19q deletion in pathological diagnosis of glioma types. [Methods] One hundred and thirty four patients with pathologically confirmed grade Ⅱ~Ⅲ glioma were included in the study. The deletion of chromosome 1 p and 19q in tumor tissues were detected by specific amplification fragment analysis. [Results] Histopathology demonstrated that of 134 patients,there were 9 cases(6.7%) of anaplastic oligodendroglioma(AO,WHO Ⅲ),15 cases(11.2%) of oligodendroglioma(OT,WHO Ⅱ),32 cases(23.9%) of mixed glioma(oligodendrocytes with astrocytic ingredients),78 cases(58.2%) of astrocytoma(AA). Heterozygous deletion rates of 1p and 19q in OT,AO,mixed glioma,AA were 73.3%(11/15) and 66.7%(10/15),66.7%(6/9) and 77.8%(7/9),53.1%(17/32) and 59.4%(19/32),43.6%(34/78) and 41.0%(32/78),respectively. There were significant differences in distribution of chromosome 1P and 19q status(intact,loss of heterozygosity,co-deletion) among OT+AO,mixed glioma and AA(P<0.05),while there was no significant difference between OT and AO. [Conclusion] The deletion of chromosome 1p and 19q is related to the pathological types of glioma,indicating that it might be of value for diagnosis of glioma types. |
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