Knüchel R, Mittermayer C, Böcking A
HNO. 1986 Jun;34(6):223-8.
Macroscopically and microscopically precancerous lesions of the oral mucosa cannot be diagnosed with sufficient accuracy. Dysplasias represent a particular diagnostic difficulty. The reproducibility of grading of dysplasias may be increased by the quantification of morphological parameters using image analysis systems. However an unequivocal identification of obligatory precancerous lesions cannot be attained by this method. Measurement of the nuclear DNA content represents a non-morphological method for the identification of obligatory precancerous lesions. The diagnostic criterion of malignancy is aneuploidy. Structural or numerical chromosomal aberrations that are absent in benign tumours and normal cells typify aneuploidy. Aneuploidy is manifested by an atypical nuclear DNA distribution that can be identified objectively by suitable algorithms. Dysplasias of the squamous epithelium with aneuploid nuclear DNA contents are regarded as obligatory precancerous lesions. DNA measurements, computation of data and printout of a 'DNA diagnosis' are possible with a TV-image analysis system and an automated microscope within 30 min.
口腔黏膜的癌前病变在宏观和微观层面都无法得到足够准确的诊断。发育异常存在特殊的诊断困难。通过使用图像分析系统对形态学参数进行量化,发育异常分级的可重复性可能会提高。然而,用这种方法无法明确识别必然的癌前病变。测量核DNA含量是一种识别必然癌前病变的非形态学方法。恶性肿瘤的诊断标准是非整倍体。良性肿瘤和正常细胞中不存在的结构或数量染色体畸变是典型的非整倍体特征。非整倍体表现为非典型的核DNA分布,可通过合适的算法进行客观识别。具有非整倍体核DNA含量的鳞状上皮发育异常被视为必然的癌前病变。利用电视图像分析系统和自动显微镜,30分钟内即可完成DNA测量、数据计算以及“DNA诊断”打印输出。