• 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

相似文献

1
Unusual sites of Rosai-Dorfman disease in children: 5 years experience from tertiary care paediatric haemato-oncology centre.儿童Rosai-Dorfman病的罕见发病部位:来自三级儿科血液肿瘤中心的5年经验
Sudan J Paediatr. 2022;22(1):109-115. doi: 10.24911/SJP.106-1623391582.
2
Rosai-Dorfman disease: A rare clinico-pathological presentation.罗萨伊-多夫曼病:一种罕见的临床病理表现。
Australas Med J. 2014 Feb 28;7(2):68-72. doi: 10.4066/AMJ.2014.1931. eCollection 2014.
3
A unique combination of Rosai-Dorfman disease and mycosis fungoides: a case report.罗萨伊-多夫曼病与蕈样肉芽肿的独特组合:一例报告
SAGE Open Med Case Rep. 2018 May 22;6:2050313X18772195. doi: 10.1177/2050313X18772195. eCollection 2018.
4
Unusual presentation of Rosai-Dorfman disease (RDD) in the bone in adolescents.青少年骨内Rosai-Dorfman病(RDD)的不典型表现
Fetal Pediatr Pathol. 2011;30(6):442-7. doi: 10.3109/15513815.2011.618873. Epub 2011 Oct 25.
5
Extra nodal Rosai Dorfman disease masquerading as metastatic soft tissue sarcoma- A case report.伪装成转移性软组织肉瘤的结外Rosai-Dorfman病——一例报告
J Clin Orthop Trauma. 2021 Jul 8;20:101500. doi: 10.1016/j.jcot.2021.101500. eCollection 2021 Sep.
6
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease): A case report and review of 49 cases with fine needle aspiration cytology.伴巨大淋巴结病的窦性组织细胞增生症(罗萨伊-多夫曼病):1例病例报告及49例细针穿刺细胞学检查病例回顾
Cytojournal. 2011 Feb 12;8:3. doi: 10.4103/1742-6413.76731.
7
Cutaneous Rosai-Dorfman Disease presenting as a flank swelling.表现为侧腹肿胀的皮肤型罗萨伊-多夫曼病
Int J Health Sci (Qassim). 2014 Oct;8(4):434-8.
8
Orbital rosai-dorfman disease in a five-year-old boy.一名五岁男孩的眼眶罗萨伊-多夫曼病
Middle East Afr J Ophthalmol. 2011 Oct;18(4):323-5. doi: 10.4103/0974-9233.90138.
9
Isolated Extranodal Rosai-Dorfman Disease on 18F-FDG PET-CT Scan.18F-FDG PET-CT扫描显示的孤立性结外Rosai-Dorfman病
Indian J Nucl Med. 2019 Oct-Dec;34(4):319-320. doi: 10.4103/ijnm.IJNM_152_19.
10
Three Cases of Extranodal Rosai-Dorfman Disease and Literature Review.三例结外Rosai-Dorfman病及文献复习
Open Life Sci. 2018 Aug 21;13:263-268. doi: 10.1515/biol-2018-0032. eCollection 2018 Jan.

本文引用的文献

1
Rosai-Dorfman Disease-Utility of 18F-FDG PET/CT for Initial Evaluation and Follow-up.罗萨达-多夫曼病 - 18F-FDG PET/CT 用于初始评估和随访的效用。
Clin Nucl Med. 2020 Jun;45(6):e260-e266. doi: 10.1097/RLU.0000000000003014.
2
Manifestations of Pediatric Extranodal Rosai Dorfman Disease in the head and neck.儿童头颈部结外Rosai-Dorfman病的表现
Int J Pediatr Otorhinolaryngol. 2020 Apr;131:109851. doi: 10.1016/j.ijporl.2019.109851. Epub 2019 Dec 26.
3
Activating mutations in CSF1R and additional receptor tyrosine kinases in histiocytic neoplasms.在组织细胞肿瘤中 CSF1R 和其他受体酪氨酸激酶的激活突变。
Nat Med. 2019 Dec;25(12):1839-1842. doi: 10.1038/s41591-019-0653-6. Epub 2019 Nov 25.
4
Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease.罗萨-多夫曼-德斯东贝病的诊断和临床管理共识建议。
Blood. 2018 Jun 28;131(26):2877-2890. doi: 10.1182/blood-2018-03-839753. Epub 2018 May 2.
5
F-fluoro-2-deoxyglucose positron emission-computed tomography in a rare cutaneous form of Rosai-Dorfman disease: A case report.氟代脱氧葡萄糖正电子发射计算机断层扫描在罕见皮肤型罗萨伊-多夫曼病中的应用:一例报告
Mol Clin Oncol. 2018 Feb;8(2):236-241. doi: 10.3892/mco.2017.1507. Epub 2017 Nov 21.
6
Rosai-Dorfman disease: a report of eight cases in a tertiary care center and a review of the literature.罗萨伊-多夫曼病:一家三级医疗中心的8例报告及文献综述
Braz J Med Biol Res. 2015 Jan;48(1):6-12. doi: 10.1590/1414-431X20144110. Epub 2014 Oct 10.
7
FDG PET/CT findings in purely cutaneous Rosai-Dorfman disease.单纯皮肤型罗道尔夫病的 FDG PET/CT 表现。
Clin Nucl Med. 2011 Apr;36(4):e13-5. doi: 10.1097/RLU.0b013e31820aa36d.
8
Neutrophil phagocytosis by tumor cells--a cytological study.肿瘤细胞对中性粒细胞的吞噬作用——一项细胞学研究。
Diagn Cytopathol. 2011 Aug;39(8):553-5. doi: 10.1002/dc.21421. Epub 2010 Oct 14.
9
Imatinib as a treatment option for systemic non-Langerhans cell histiocytoses.伊马替尼作为系统性非朗格汉斯细胞组织细胞增多症的一种治疗选择。
Arch Dermatol. 2007 Jun;143(6):736-40. doi: 10.1001/archderm.143.6.736.
10
Parvovirus B19 detected in Rosai-Dorfman disease in nodal and extranodal manifestations.在Rosai-Dorfman病的淋巴结和结外表现中检测到细小病毒B19 。
J Clin Pathol. 2006 Dec;59(12):1320-6. doi: 10.1136/jcp.2005.029850.

儿童Rosai-Dorfman病的罕见发病部位:来自三级儿科血液肿瘤中心的5年经验

Unusual sites of Rosai-Dorfman disease in children: 5 years experience from tertiary care paediatric haemato-oncology centre.

作者信息

Arul Janani, Kataria Riya, Kolli Varsha, Murali Arunan, Vasugi Gramani Arumugam, Srinivasan Arathi

机构信息

Department of Paediatric Oncology, Sri Ramachandra Medical College and Research Institute, Chennai, Tamil Nadu.

MBBS Student, Sri Ramachandra Medical College and Research Institute, Chennai, Tamil Nadu.

出版信息

Sudan J Paediatr. 2022;22(1):109-115. doi: 10.24911/SJP.106-1623391582.

DOI:10.24911/SJP.106-1623391582
PMID:35958069
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9361499/
Abstract

Rosai-Dorfman disease (RDD) is a rare histiocytic disorder, usually presenting with massive lymphadenopathy. The involvement of extra nodal sites, bone and nodal sites like mediastinum are rare. Clinical data of three cases of extra nodal RDD who were admitted in our paediatric haemato-oncology unit were analysed in the last 5 years. The extra nodal RDD (maxillary sinus, nasal pharyngeal focus, and external auditory meatus) were diagnosed based on histopathology and positron emission tomography scan. They were treated with steroids but were refractory hence requiring salvage chemotherapy. Currently all three of them are in complete remission. Extra nodal RDD is difficult to diagnose, histopathology and radiology play an important role. Here, we present three cases, of which two were steroid-refractory which were treated with salvage chemotherapy and are in complete remission.

摘要

罗萨伊-多夫曼病(RDD)是一种罕见的组织细胞疾病,通常表现为巨大淋巴结病。结外部位、骨骼以及纵隔等淋巴结部位受累较为罕见。对过去5年在我们儿科血液肿瘤病房收治的3例结外RDD患者的临床资料进行了分析。这些结外RDD(上颌窦、鼻咽部病灶和外耳道)通过组织病理学和正电子发射断层扫描进行诊断。他们接受了类固醇治疗,但效果不佳,因此需要挽救性化疗。目前他们三人都处于完全缓解状态。结外RDD难以诊断,组织病理学和放射学起着重要作用。在此,我们报告3例病例,其中2例对类固醇治疗无效,接受了挽救性化疗并处于完全缓解状态。