• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Secondary Burkitt lymphoma in a retinoblastoma patient with 13q deletion syndrome.

作者信息

Hongeng Suradej, Parapakpenjun Surapan, Pakakasama Samart, Rerkamnuaychoke Busaba, Pornkul Ratanaporn

机构信息

Department of Pediatrics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

出版信息

Pediatr Blood Cancer. 2006 Apr;46(4):524-6. doi: 10.1002/pbc.20372.

DOI:10.1002/pbc.20372
PMID:15926151
Abstract

We report a boy with constitutional deletion 13q chromosome associated with dysmorphic features and bilateral retinoblastoma. The patient developed secondary Burkitt lymphoma 5 years after the diagnosis of retinoblastoma at the age of 8 months. He has completed treatment for both malignancies. At present, he is 7 years old and still in remission.

摘要

相似文献

1
Secondary Burkitt lymphoma in a retinoblastoma patient with 13q deletion syndrome.
Pediatr Blood Cancer. 2006 Apr;46(4):524-6. doi: 10.1002/pbc.20372.
2
Retinoblastoma and deletion of the long arm of chromosome 13: an underestimated diagnosis?
Pediatr Blood Cancer. 2008 Mar;50(3):694-6. doi: 10.1002/pbc.20963.
3
The importance of excluding 13q deletion mosaicism in the diagnosis of retinoblastoma associated with dysmorphic features.
Genet Couns. 2005;16(1):91-3.
4
Axenfeld-Rieger ocular anomaly and retinoblastoma caused by constitutional chromosome 13q deletion.Axenfeld-Rieger 眼异常和视网膜母细胞瘤由 13q 染色体结构缺失引起。
Pediatr Blood Cancer. 2010 Mar;54(3):480-2. doi: 10.1002/pbc.22354.
5
[Bilateral non-Hodgkin's lymphoma of the kidneys as the only manifestation].[双侧肾脏非霍奇金淋巴瘤作为唯一表现]
Urologe A. 1996 Jan;35(1):51-3.
6
Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.49例原发性视网膜母细胞瘤肿瘤的比较基因组杂交确定了与组织病理学、进展及患者预后相关的染色体区域。
Genes Chromosomes Cancer. 2003 Feb;36(2):121-8. doi: 10.1002/gcc.10149.
7
Chromosome 13q deletion with Cornelia de Lange syndrome phenotype.
Med J Malaysia. 2007 Mar;62(1):74-5.
8
[Monosomy 13q syndrome].
Ryoikibetsu Shokogun Shirizu. 2000(30 Pt 5):329-31.
9
Incidence of new tumor formation in patients with hereditary retinoblastoma treated with primary systemic chemotherapy: is there a preventive effect?接受原发性全身化疗的遗传性视网膜母细胞瘤患者新肿瘤形成的发生率：是否存在预防作用？
Ophthalmology. 2007 Nov;114(11):2077-82. doi: 10.1016/j.ophtha.2007.03.015. Epub 2007 Jul 12.
10
Bone marrow transplantation for therapy-related acute myeloid leukemia in congenital retinoblastoma associated with 13q deletion syndrome.骨髓移植治疗与13q缺失综合征相关的先天性视网膜母细胞瘤中的治疗相关急性髓系白血病。
Ann Hematol. 2004 Jul;83(7):481-3. doi: 10.1007/s00277-004-0884-5. Epub 2004 May 11.

引用本文的文献

1
Minimal exposure intra-arterial chemotherapy for children with retinoblastoma and 13q syndrome.视网膜母细胞瘤合并13q综合征患儿的最小暴露量动脉内化疗
Oman J Ophthalmol. 2016 Sep-Dec;9(3):164-166. doi: 10.4103/0974-620X.192278.