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肾癌多中心病灶发生机理的探讨 被引量:29

Study of the genesis of multicentricity in renal cell carcinoma
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摘要 目的 探讨肾癌多中心病灶的发生机理。 方法 肾癌根治术标本 10 2例 ,间隔 3mm切开检查切面 ,原发灶外可疑处取材证实肾癌者为多中心灶阳性。免疫组化法检查肾癌原发灶及多中心灶p5 3、PCNA、c erbB2 、CD44 v6、bcl 2、nm2 3 H1 蛋白表达情况。 结果 多中心灶发生率为 15 .7%( 16 10 2 ) ,16例多中心性肾癌中 ,原发灶与多中心灶p5 3、PCNA、c erbB2 、CD44 v6、bcl 2、nm2 3 H1 蛋白表达情况均相近 ,统计学处理差异无显著性意义 (P均 >0 .4)。 结论 肾癌多中心灶具有与原发灶相似的生物学特征 ,其发生以原发灶肾内转移可能性大。 ObjectiveTo study the genesis of multicentricity in renal cell carcinoma (RCC).Methods102 kidneys from radical nephrectomy for RCC were step sectioned at 3 mm intervals and examined for the presence of multifocal cancers and vascular invasion and for the condition of the pseudocapsule.Expressions of p53,PCNA,c-erb B 2,CD 44v6,bcl-2 and nm 23-H 1 in the primary and multifocal RCC were assayed by standard SP immunohistochemical procedures.ResultsOf the 102 cases,positive multifocal RCC was found in 16 (15.6%).The expressions of p53,PCNA,c-erb B 2,CD 44v6,bcl-2 and nm 23-H 1 in the primary tumors were very similar to those in the multifocal lesions without significant differences statistically (P>0.4).ConclusionsThese data denote that biological behaviors and malignant features of multifocal tumors are very similar to those of primary ones.In addition,considering the significant relationship of multicentricity with vascular invasion and incompleteness of pseudocapsule of RCC,it is suggested that the secondary tumors might be more likely the result of intrarenal metastasis of the primary tumor rather than the results of multifocal genesis.
出处 《中华泌尿外科杂志》 CAS CSCD 北大核心 2003年第4期232-234,共3页 Chinese Journal of Urology
基金 辽宁省教育厅科研基金资助项目 ( 980 42 110 36 )
关键词 肾癌 多中心病灶 发生机理 生物学特征 Kidney neoplasms Carcinoma Neoplasms,multiple primary
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参考文献8

  • 1邹高德,葛根,孙锡林,庄文华,吴绮明,张文昌.肾细胞癌抗凋亡基因bcl-2的免疫组化研究[J].中华泌尿外科杂志,1997,18(6):329-331. 被引量:12
  • 2范小玲,张祥生,郝元瑞,李启忠,单磊,郝元瑞.CD_(44)和nm23在肾脏肿瘤中表达及其临床意义[J].中华泌尿外科杂志,1999,20(9):551-553. 被引量:2
  • 3Junker K, Schlichter A, Hindermann W, et al. Genetic characterization of multifocal tumor growth in renal cell carcinoma. Kidney Int, 1999,56 : 1291-1294.
  • 4Haitel A, Wiener HG, Blasehitz U, et al. Biologic behavior of p53 overexpression in multifocal renal cell carcinoma of clear cell type.Cancer, 1999,85 : 1593-1598.
  • 5Morel QL, Clar BF, Fenollosa EB, et al. Proliferating cell nuclear antigen (PCNA) as a prognostic factor in renal cell carcinoma. Anticancer Res, 1998,18:677-682.
  • 6Paradis V, Ferlicot S, Ghannam E, et al. CD44 is an independent prognostic factor in conventional renal cell carcinoma. J Urol, 1999,16 :1984-1987.
  • 7Stumm G, Eberwein S, Rostock-Wolf S, et al. Concomitant overexpression of the EGFR and erb B2 genes in renal cell carcinoma(RCC) is correlated with dedifferentiation and metastasis. Int J Cancer, 1996,69:17-22.
  • 8Eschewege P,Saunsine C,Delepaul B,et al. Radical nephrectomy for renal cell carcinoma 30 mm or less :long-term followup results. J Urol,1996,155 : 1196-1199.

二级参考文献1

  • 1夏红,肿瘤防治研究,1995年,22卷,54页

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