首页> 外文期刊>The Open Pathology Journal >Primary Rectal Mucosa-Associated Lymphoid Tissue Lymphoma: Report of a Case with Extensive FISH Study
【24h】

Primary Rectal Mucosa-Associated Lymphoid Tissue Lymphoma: Report of a Case with Extensive FISH Study

机译:原发性直肠粘膜相关淋巴组织淋巴瘤:广泛的FISH研究的一例报告。

获取原文
       

摘要

Primary rectal mucosa-associated lymphoid tissue (MALT) lymphoma is a very rare entity with scarce cytogenetic/molecular genetic data. We presented a polypoid rectal MALT lymphoma in a 75 year-old male. The tumor comprisedsmall atypical lymphocytes forming focal lymphoepithelial lesions and expressing CD20 but not CD5, CD23,CD43, or cyclin D1. They were negative for translocations involving IGH, MALT1, BCL2, BCL6, and CCND1 genes, andthe copy numbers of chromosomes 3, 12, and 18 were normal by fluorescent in situ hybridization. The patient was disease-free for 83 months after oral endoxan and prednisolone and concurrent local radiotherapy. With increasing awarenessof this disease and accumulating reports on clinicopathological and molecular data, the pathogenesis, best treatment strategyand clinical course of such tumors will be uncovered.
机译:原发性直肠粘膜相关淋巴样组织(MALT)淋巴瘤是一种非常罕见的实体,缺乏细胞遗传学/分子遗传学数据。我们介绍了一位75岁男性息肉样直肠MALT淋巴瘤。肿瘤包括小的非典型淋巴细胞,形成局灶性淋巴上皮病变,表达CD20,但不表达CD5,CD23,CD43或细胞周期蛋白D1。它们对涉及IGH,MALT1,BCL2,BCL6和CCND1基因的易位呈阴性,并且通过荧光原位杂交,染色体3、12和18的拷贝数正常。口服内毒素和泼尼松龙并同时进行局部放疗后,患者无病83个月。随着对这种疾病的认识的提高以及有关临床病理和分子数据的报道的积累,这些肿瘤的发病机理,最佳治疗策略和临床过程将被发现。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号