구강편평세포암종의 유세포분석적 DNA측정을 위한 이중 매개변수법의 적용

APPLICATION OF DUAL PARAMETER ANALYSIS IN FLOW CYTOMETRIC DNA MEASUREMENTS OF ORAL SQUAMOUS CELL CARCINOMA

  • 김수야 (전북대학교 치과대학 소아치과학교실) ;
  • 주훈 (전북대학교 치과대학 소아치과학교실) ;
  • 김재곤 (전북대학교 치과대학 소아치과학교실) ;
  • 조남표 (전북대학교 치과대학 구강병리학교실) ;
  • 백병주 (전북대학교 치과대학 소아치과학교실)
  • Kim, Su-Ya (Dept. of Pediatric Dentistry College of Dentistry, Chonbuk National University) ;
  • Ju, Hoon (Dept. of Pediatric Dentistry College of Dentistry, Chonbuk National University) ;
  • Kim, Jae-Gon (Dept. of Pediatric Dentistry College of Dentistry, Chonbuk National University) ;
  • Cho, Nam-Pyo (Dept. of Oral Pathology College of Dentistry, Chonbuk National University) ;
  • Baik, Byeong-Ju (Dept. of Pediatric Dentistry College of Dentistry, Chonbuk National University)
  • 발행 : 1996.05.31

초록

A series of 31 patients with primary oral squamous cell carcinoma (SCC) who were treated at Chonbuk National University Hospital during the years 1991-1995, were evaluated by dual parameter analysis in flow cytometric DNA measurement, Bryne's malignancy grading system, and the TNM classification. The aims of the present study were to discover that previously undetected aneuploid clones could be detected by dual parameter analysis and to determine the prognostic value of the above parameters. 1. Using dual parameter analysis of cytokeratin and DNA on disintegrated paraffin-embedded samples, aneuploid clones which were undetected by regular single parameter DNA analysis could be found among the cytokeratin-selected cells. DNA aneuploidy from paraffin-embedded samples were 15 cases compared with 10 cases using conventional DNA analysis. 2. The portion of aneuploid tumors showed slightly higher clinical stage and tumor size than the portion of diploid tumors, but the difference was not significant. The portion of DNA aneuploid tumors showed significantly higher mean mitosis and total malignancy scores than the portion of DNA diploid tumors. 3. The majority of the patients presented with clinical stage III and IV lesions showed significantly higher mean total malignancy score as compared to those with clinical stage I and II. 4. Histopathologic mean total malignancy score of the 31 cases was 12.7. Among the histologic parameters, mean mitosis score was correlated to the status of DNA ploidy and total malignancy score were correlated to the DNA ploidy and clinical staging.

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