期刊文献+

弥漫性大B细胞淋巴瘤500例构成比及免疫表型分析 被引量:22

Immunophenotypes and prognosis of diffuse large B-cell lymphoma : a study of 500 cases
原文传递
导出
摘要 目的按照WHO(2008版)造血与淋巴组织肿瘤分类,分析弥漫性大B细胞淋巴瘤(DLBCL)各亚型的构成比情况、免疫表型特点,及其总体生存率。方法按照新分类,结合形态学观察,利用免疫组织化学、基因重排、原位杂交、荧光原位杂交(FISH)等技术对500例DLBCL,进行回顾性分析和归类,收集随访资料,并对生发中心B细胞(GCB)型和非GCB型组之间、老年人EB病毒(EBV)阳性的DCBCL亚型和非特殊型弥漫性大B细胞淋巴瘤(DLBCL—NOS)之间进行总体生存率比较。结果500例中DLBCL—NOS约占77.2%(386/500),其次是老年人EBV阳性的DLBCL占9.4%(47/500),然后依次是原发中枢神经系统的DLBCL(4.4%,22/500)、原发纵隔(胸腺)的大B细胞淋巴瘤(2.8%,14/500)、富于T细胞/组织细胞的大B细胞淋巴瘤(2.6%,13/500),其余类型均属于比较罕见的。DLBCL—NOS按照形态学分类以中心母细胞性最为常见,约占95.1%(367/386);按免疫组织化学分型,非GCB型组在DLBCL—NOS中约占68.5%(219/320),GCB型组占28.4%(91/320),而CD5阳性DLBCL仅占3.1%(10/320)。总体生存率比较,GCB型组和非GCB型组总体生存率差异无统计学意义(P=0.93),老年人EBV阳性的DLBCL组总体生存率与年龄匹配前、后的DLBCL—NOS组差异均无统计学意义(P值分别为0.13和0.28)。对形态学表现为灰区的淋巴瘤病例进行FISH检测,发现了1例“双打击”(double—hit)淋巴瘤。结论DLBCL—NOS在DLBCL中占绝大多数,其次是老年人EBV阳性的DLBCL和原发中枢神经系统的DLBCL,其他类型均属少见或罕见类型。按照Hans分类进行免疫组织化学分型,非GCB型占多数,GCB型和非GCB型分组总体生存率没有显著性差异。老年人EBV阳性的DLBCL组和用年龄匹配前后的DLBCL—NOS组的总体生存率均无显著性差异。 Objective To study the immunophenotype and overall survival of diffuse large B-cell lymphoma (DLBCL) classified according to the 2008 World Health Organization classification of tumors of hematopoietic and lymphoid tissues. Methods Five hundred cases of DLBCL were retrospectively analyzed with histologic review, immunohistochemistry, gene rearrangement study, in situ hybridization and fluorescence in situ hybridization. Follow-up data were collected. The overall survival rates of germinal center B-cell (GCB) and non-germinal center B-cell (non-GCB) subtypes, as well as those of DLBCL, not otherwise specified (NOS) and Epstein-Barr virus (EBV)-positive DLBCL of the elderly, were compared. Results DLBCL-NOS was the commonest subtype which accounted for 77.2% (386/500) of the cases. EBV-positive DLBCL of the elderly, primary DLBCL of central nervous system, primary mediastinal (thymic) large B-cell lymphoma and T cell/histiocyte-rich large B-cell lymphoma accounted for 9.4% (47/500), 4.4% (22/500), 2. 8% (14/500) and 2.6% ( 13/500), respectively. 68.5% (219/320) of DLBCL-NOS belonged to non-GCB subtype. The percentage of GCB subtype and CD5-positive subtype were 28.4% (91/320) and 3. 1% (10/320), respectively. Comparison of the overall survival, GCB and non-GCB immunophenotypic groups have no significant difference (P = 0. 93 ). And the same result in which of the EBV-positive DLBCL of the elderly and DLBCL-NOS group, before and after age matched (P = 0. 13 and 0. 28, respectively). A double-hit lymphoma was found by FISH detection, which presenting as gray zone lymphoma in morphology. Conclusions By using Hans algorithm, GCB and non-GCB subtypes show no significant difference in overall survival. EBV-positive DLBCL of the elderly and DLBCL-NOS also do not have significant difference in overall survival. Fluorescence in situ hybridization technique is helpful in identification of DLBCL with rare phenotypes.
出处 《中华病理学杂志》 CAS CSCD 北大核心 2011年第4期235-239,共5页 Chinese Journal of Pathology
关键词 淋巴瘤 大细胞 弥漫型 免疫表型分型 生存率分析 Lympthoma,large-cell,diffuse Immunophenotyping Survival analysis
  • 相关文献

二级参考文献10

  • 1Ramsay A,Smith W,Isaacson P.T-cell-rich B-cell lymphoma.Am J Surg Pathol,1988,12:433-443. 被引量:1
  • 2Gatter KC,Warnke R.Diffuse large B-cell lymphomas.In:Jaffe ES,Harris NL,Stein H,et al.eds.World Health Organization classification of tumors:pathology and genetics of tumors of haematopoietic and lymphoid tissues.Lyon:IARC Press,2001.171-174. 被引量:1
  • 3Lim MS,Beaty M,Sorbara L,et al.T-cell/histiocyte-rich large cell lymphoma.A heterogenerous entity with deriration from germinal center B cells.Am J Surg Pathol,2002,26:1458-1466. 被引量:1
  • 4Dogan A,Burke JS,Goteri G,et al.Micronodular T-cell/histiocyte-rich large B-cell lymphoma of the spleen.Histology,immunophenotype,and differential diagnosis.Am J Surg Pathol,2003,27:903-911. 被引量:1
  • 5Fan Z,Natkunam Y,Bair E,et al.Characterization of variant patterns of nodular lymphocyte predominant Hodgkin lymphoma with immunohistologic and clinical correlation.Am J Surg Pathol,2003,27:1346-1356. 被引量:1
  • 6Boudova L,Torlakovic YE,Delabie J,et al.Nodular lymphocyte-predominant Hodgkin lymphoma with nodules resembling T-cell/histiocyte-rich B-cell lymphoma:differential diagnosis between nodular lymphocyte-predominant Hodgkin lymphoma and T-cell/histiocyte-rich B-cell lymphoma.Blood,2003,102:3753-3758. 被引量:1
  • 7Harris NL.Hodgkin's Disease:classification and differential diagnosis.Mod Pathol,1999,12:159-176. 被引量:1
  • 8李甘地.霍奇金淋巴瘤的病理诊断和鉴别诊断[J].临床与实验病理学杂志,1999,15(1):68-71. 被引量:18
  • 9廖新波,庄恒国,骆新兰,蔡秀玲.富于T细胞/组织细胞的B细胞淋巴瘤的诊断[J].临床与实验病理学杂志,2000,16(6):454-457. 被引量:4
  • 10刘艳辉,朱雄增,庄恒国,林汉良,吴秋良,蒋光愉,顾莹莹,罗东兰,骆新兰.结节性淋巴细胞为主型霍奇金淋巴瘤的诊断与鉴别诊断[J].中华病理学杂志,2002,31(3):227-230. 被引量:10

共引文献19

同被引文献251

引证文献22

二级引证文献131

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部