• 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
Paediatric desmoid tumour of the head and neck: a complete response to chemotherapy and the paradigm shift towards non-surgical management.头颈部儿科侵袭性纤维瘤病:化疗完全缓解和向非手术治疗模式转变。
BMJ Case Rep. 2021 Jan 12;14(1):e237509. doi: 10.1136/bcr-2020-237509.
2
Desmoid tumours of the head and neck in children: Review of management.儿童头颈部硬纤维瘤:治疗综述
Eur Ann Otorhinolaryngol Head Neck Dis. 2017 May;134(3):155-160. doi: 10.1016/j.anorl.2016.11.007. Epub 2016 Dec 14.
3
Desmoid-type fibromatosis of the head and neck in children: A changing situation.儿童头颈部韧带样型纤维瘤病:形势变迁
Int J Pediatr Otorhinolaryngol. 2019 Aug;123:33-37. doi: 10.1016/j.ijporl.2019.04.037. Epub 2019 Apr 26.
4
Desmoid tumours of the head and neck: A case report.头颈部韧带样瘤:病例报告。
Eur Ann Otorhinolaryngol Head Neck Dis. 2019 Jun;136(3):207-209. doi: 10.1016/j.anorl.2019.02.008. Epub 2019 Mar 14.
5
Chemotherapy of locally aggressive head and neck tumors in the pediatric age group. Desmoid fibromatosis and nasopharyngeal angiofibroma.小儿年龄组局部侵袭性头颈部肿瘤的化疗。韧带样纤维瘤病和鼻咽血管纤维瘤。
Am J Surg. 1982 Oct;144(4):437-44. doi: 10.1016/0002-9610(82)90418-4.
6
Imatinib induces sustained progression arrest in RECIST progressive desmoid tumours: Final results of a phase II study of the German Interdisciplinary Sarcoma Group (GISG).伊马替尼可使RECIST标准判定为进展期的硬纤维瘤出现持续的病情进展停滞:德国跨学科肉瘤研究组(GISG)一项II期研究的最终结果
Eur J Cancer. 2017 May;76:60-67. doi: 10.1016/j.ejca.2017.02.001. Epub 2017 Mar 8.
7
Extra-abdominal desmoid fibromatosis--a sarcoma unit review of practice, long term recurrence rates and survival.腹外硬纤维瘤病——肉瘤诊疗单位的实践、长期复发率及生存率回顾
Eur J Surg Oncol. 2014 Sep;40(9):1125-30. doi: 10.1016/j.ejso.2014.02.226. Epub 2014 Feb 22.
8
Desmoid tumour of the neck: complete regression following radiation therapy.颈部硬纤维瘤:放射治疗后完全消退
J Laryngol Otol. 2002 Jun;116(6):477-9. doi: 10.1258/0022215021911121.
9
Is photodynamic therapy a good alternative to surgery and radiotherapy in the treatment of head and neck cancer?光动力疗法在头颈部癌的治疗中是手术和放疗的良好替代方案吗?
Photodiagnosis Photodyn Ther. 2009 Mar;6(1):3-11. doi: 10.1016/j.pdpdt.2009.03.002. Epub 2009 May 5.
10
Treatment of non-metastatic rhabdomyosarcomas in childhood and adolescence. Results of the second study of the International Society of Paediatric Oncology: MMT84.儿童和青少年非转移性横纹肌肉瘤的治疗。国际儿科肿瘤学会第二项研究(MMT84)的结果
Eur J Cancer. 1998 Jun;34(7):1050-62. doi: 10.1016/s0959-8049(98)00024-0.

本文引用的文献

1
Cryoablation of Extra-Abdominal Desmoid Tumors: A Single-Center Experience with Literature Review.腹外硬纤维瘤的冷冻消融:单中心经验及文献综述
Diagnostics (Basel). 2020 Aug 4;10(8):556. doi: 10.3390/diagnostics10080556.
2
The management of desmoid tumours: A joint global consensus-based guideline approach for adult and paediatric patients.《韧带样纤维瘤的治疗管理:成人和儿童患者基于全球共识的联合指南方法》
Eur J Cancer. 2020 Mar;127:96-107. doi: 10.1016/j.ejca.2019.11.013. Epub 2020 Jan 28.
3
Facial Desmoid Tumor in a 2-Year-Old.
Ear Nose Throat J. 2020 Jan;99(1):NP3-NP5. doi: 10.1177/0145561318823647. Epub 2019 Jan 31.
4
The EpSSG NRSTS 2005 treatment protocol for desmoid-type fibromatosis in children: an international prospective case series.2005年儿童韧带样型纤维瘤病的欧洲小儿软组织肉瘤研究组(EpSSG)治疗方案:一项国际前瞻性病例系列研究
Lancet Child Adolesc Health. 2017 Dec;1(4):284-292. doi: 10.1016/S2352-4642(17)30045-7. Epub 2017 Sep 12.
5
Role of Nonsteroidal Anti-inflammatory Drug in Treatment of Extra-abdominal Desmoid Tumors.非甾体抗炎药在治疗腹外硬纤维瘤中的作用
Clin Orthop Surg. 2018 Jun;10(2):225-233. doi: 10.4055/cios.2018.10.2.225. Epub 2018 May 18.
6
Infantile Hemangiomas in the Head and Neck Region.头颈部的婴儿血管瘤
Otolaryngol Clin North Am. 2018 Feb;51(1):77-87. doi: 10.1016/j.otc.2017.09.009.
7
Effective treatment of aggressive fibromatosis with celecoxib guided by genetic testing.基于基因检测的塞来昔布靶向治疗侵袭性纤维瘤病
Cancer Biol Ther. 2017 Oct 3;18(10):757-760. doi: 10.1080/15384047.2017.1373215. Epub 2017 Sep 7.
8
Adult desmoid tumors: biology, management and ongoing trials.成人韧带样瘤:生物学特性、治疗及正在进行的试验
Curr Opin Oncol. 2017 Jul;29(4):268-274. doi: 10.1097/CCO.0000000000000374.
9
Desmoid tumours of the head and neck in children: Review of management.儿童头颈部硬纤维瘤:治疗综述
Eur Ann Otorhinolaryngol Head Neck Dis. 2017 May;134(3):155-160. doi: 10.1016/j.anorl.2016.11.007. Epub 2016 Dec 14.
10
Complete remission of pancreatic head desmoid tumor treated by COX-2 inhibitor-a case report.COX-2抑制剂治疗胰头韧带样瘤完全缓解——病例报告
World J Surg Oncol. 2016 Jul 22;14(1):190. doi: 10.1186/s12957-016-0944-z.

头颈部儿科侵袭性纤维瘤病:化疗完全缓解和向非手术治疗模式转变。

Paediatric desmoid tumour of the head and neck: a complete response to chemotherapy and the paradigm shift towards non-surgical management.

机构信息

Department of Neuroradiology, Centro Hospitalar Universitário Lisboa Norte EPE, Lisboa, Portugal.

Department of Paediatrics, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisboa, Portugal.

出版信息

BMJ Case Rep. 2021 Jan 12;14(1):e237509. doi: 10.1136/bcr-2020-237509.

DOI:10.1136/bcr-2020-237509
PMID:33436358
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7805379/
Abstract

Desmoid tumours are rare locally aggressive mesenchymal tumours with a high local recurrence rate, particularly in the head and neck locations. We present the case of a 5-year-old child with a locally invasive inoperable desmoid tumour of the masticator space who underwent a low-dose chemotherapy regimen for 17 months, obtaining a long-term complete response. Definitive evidenced-based treatment guidelines are lacking. Therefore, paediatric patients should be managed by specialised multidisciplinary teams to try to achieve the best tumour control while minimising treatment associated morbidity and mortality. Available treatment options include surgery, radiotherapy and different systemic medical therapies. Whereas traditionally, surgery was the mainstay of treatment, more conservative options have increasingly shown adequate tumour control with little associated morbidity. In this decision making it is mandatory to take into account the patient's age, tumour location and extension, and potential short-term and long-term treatment-related sequelae to minimise functional and cosmetic compromise.

摘要

硬纤维瘤是一种罕见的局部侵袭性间叶组织肿瘤,局部复发率高,特别是在头颈部。我们报告了一例 5 岁儿童,患有咀嚼肌间隙局部侵袭性不可切除的硬纤维瘤,接受了 17 个月的低剂量化疗方案,获得了长期完全缓解。目前缺乏明确的循证治疗指南。因此,儿科患者应由专门的多学科团队进行管理,以尽量在降低治疗相关发病率和死亡率的同时,实现最佳肿瘤控制。现有的治疗选择包括手术、放疗和不同的全身药物治疗。传统上,手术是治疗的主要手段,但越来越多的保守选择已显示出足够的肿瘤控制效果,相关发病率较低。在这一决策过程中,必须考虑到患者的年龄、肿瘤位置和范围,以及潜在的短期和长期治疗相关后遗症,以尽量减少功能和美容方面的损害。