• 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

非洲黑人队列中的隆突性皮肤纤维肉瘤——一项临床病理研究

Dermatofibrosarcoma protuberance in a black African cohort-a clinicopathologic study.

作者信息

Ogun Gabriel Olabiyi, Ezenkwa Uchenna Simon, Ayandipo Omobolaji Oladayo

机构信息

Department of Pathology, University of Ibadan/University College Hospital, Ibadan, 200001, Nigeria.

https://orcid.org/0000-0001-8535-3240.

出版信息

Ecancermedicalscience. 2020 Aug 7;14:1086. doi: 10.3332/ecancer.2020.1086. eCollection 2020.

DOI:10.3332/ecancer.2020.1086
PMID:33014128
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7498272/
Abstract

BACKGROUND

Dermatofibrosarcoma protuberance (DFSP) is the commonest, yet rare, dermal sarcoma globally. There are few reports in the literature of this neoplasm in Nigerians and indeed in sub-Saharan Africa. This study documents our institutional practice observation and compares it with those from other regions of the world.

METHODS AND MATERIALS

This study was a retrospective review of all cases of histologically diagnosed DFSP at the University College Hospital, Ibadan, Nigeria, spanning a period of 27 years (January 1989-December 2016). Data on patient age, gender, tumour location, size, tumour recurrence and metastasis status were obtained from clinical and surgical pathology archival files and records.

RESULTS

Sixty-nine cases of DFSP were recorded over the period reviewed with a male-female ratio of 1.6:1. The mean age of the study population was 39.6 years. The youngest patient was 5-year old, while the oldest was 86 years and the modal age group was the 4th decade. The trunk was the commonest anatomic tumour location. Recurrences were seen in seven cases with recurrence interval ranging from 6 to 240 months. The correlation between tumour size and age was non-significant ( = -0.183; = 0.182). There was fibrosarcoma-like transformation in three cases (4.3%) studied.

CONCLUSION

Dermatofibrosarcoma protuberance is rare in our population and occurs more commonly in males and on the trunk. Recurrence can occur beyond the recommended follow-up period of 10 years.

摘要

背景

隆突性皮肤纤维肉瘤(DFSP)是全球最常见但却罕见的皮肤肉瘤。关于尼日利亚人乃至撒哈拉以南非洲地区这种肿瘤的文献报道很少。本研究记录了我们机构的实际观察情况,并将其与世界其他地区的情况进行比较。

方法和材料

本研究是对尼日利亚伊巴丹大学学院医院27年(1989年1月至2016年12月)期间所有经组织学诊断为DFSP的病例进行的回顾性研究。从临床和外科病理档案及记录中获取患者年龄、性别、肿瘤位置、大小、肿瘤复发和转移状况的数据。

结果

在回顾期间共记录了69例DFSP病例,男女比例为1.6:1。研究人群的平均年龄为39.6岁。最年轻的患者为5岁,最年长的为86岁,发病高峰年龄组为第四十年龄段。躯干是最常见的肿瘤解剖位置。7例出现复发,复发间隔时间为6至240个月。肿瘤大小与年龄之间的相关性不显著( = -0.183; = 0.182)。在研究的3例(4.3%)病例中出现了纤维肉瘤样转化。

结论

隆突性皮肤纤维肉瘤在我们的人群中很罕见,在男性和躯干上更常见。复发可能发生在推荐的10年随访期之后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c154/7498272/25d478cb5eaf/can-14-1086fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c154/7498272/d9a085d9011a/can-14-1086fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c154/7498272/25d478cb5eaf/can-14-1086fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c154/7498272/d9a085d9011a/can-14-1086fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c154/7498272/25d478cb5eaf/can-14-1086fig2.jpg

相似文献

1
Dermatofibrosarcoma protuberance in a black African cohort-a clinicopathologic study.非洲黑人队列中的隆突性皮肤纤维肉瘤——一项临床病理研究
Ecancermedicalscience. 2020 Aug 7;14:1086. doi: 10.3332/ecancer.2020.1086. eCollection 2020.
2
Dermatofibrosarcoma protuberans: clinicopathologic presentation in Nigerians.
Pan Afr Med J. 2018 Sep 12;31:25. doi: 10.11604/pamj.2018.31.25.13665. eCollection 2018.
3
Dermatofibrosarcoma protuberans: the diagnosis of high-grade fibrosarcomatous transformation.隆突性皮肤纤维肉瘤:高级别纤维肉瘤样转化的诊断。
Skeletal Radiol. 2021 Apr;50(4):789-799. doi: 10.1007/s00256-020-03617-3. Epub 2020 Oct 1.
4
Fibrosarcomatous ("high-grade") dermatofibrosarcoma protuberans: clinicopathologic and immunohistochemical study of a series of 41 cases with emphasis on prognostic significance.纤维肉瘤样(“高级别”)隆突性皮肤纤维肉瘤:41例系列病例的临床病理及免疫组化研究,重点关注预后意义。
Am J Surg Pathol. 1998 May;22(5):576-87. doi: 10.1097/00000478-199805000-00009.
5
Sarcomas arising in dermatofibrosarcoma protuberans: a reappraisal of biologic behavior in eighteen cases treated by wide local excision with extended clinical follow up.隆突性皮肤纤维肉瘤中发生的肉瘤:对18例行广泛局部切除并长期临床随访的病例的生物学行为重新评估
Am J Surg Pathol. 2000 Aug;24(8):1125-30. doi: 10.1097/00000478-200008000-00010.
6
Dermatofibrosarcoma protuberans: a report on 29 patients treated by Mohs micrographic surgery with long-term follow-up and review of the literature.隆突性皮肤纤维肉瘤:29例采用莫氏显微外科手术治疗患者的报告及长期随访与文献复习
Cancer. 2004 Jul 1;101(1):28-38. doi: 10.1002/cncr.20316.
7
Dermatofibrosarcoma protuberans, giant cell fibroblastoma, and hybrid lesions in children: clinicopathologic comparative analysis of 28 cases with molecular data--a study from the French Federation of Cancer Centers Sarcoma Group.儿童隆突性皮肤纤维肉瘤、巨细胞成纤维细胞瘤及混合性病变:28例临床病理比较分析及分子数据——来自法国癌症中心肉瘤研究组的一项研究
Am J Surg Pathol. 2003 Jan;27(1):27-39. doi: 10.1097/00000478-200301000-00004.
8
Low recurrence rate after surgery for dermatofibrosarcoma protuberans: a multidisciplinary approach from a single institution.隆突性皮肤纤维肉瘤手术后的低复发率:来自单一机构的多学科方法。
Cancer. 2004 Mar 1;100(5):1008-16. doi: 10.1002/cncr.20051.
9
Dermatofibrosarcoma protuberans: a population-based cancer registry descriptive study of 66 consecutive cases diagnosed between 1982 and 2002.隆突性皮肤纤维肉瘤:一项基于人群的癌症登记描述性研究,涉及1982年至2002年间连续诊断的66例病例。
J Eur Acad Dermatol Venereol. 2006 Nov;20(10):1237-42. doi: 10.1111/j.1468-3083.2006.01780.x.
10
[Pigmented dermatofibrosarcoma protuberance: a clinicopathologic analysis of 7 cases].[色素性隆突性皮肤纤维肉瘤:7例临床病理分析]
Zhonghua Bing Li Xue Za Zhi. 2013 Dec;42(12):810-4.

本文引用的文献

1
Dermatofibrosarcoma protuberans: clinicopathologic presentation in Nigerians.
Pan Afr Med J. 2018 Sep 12;31:25. doi: 10.11604/pamj.2018.31.25.13665. eCollection 2018.
2
Current Update on the Molecular Biology of Cutaneous Sarcoma: Dermatofibrosarcoma Protuberans.皮肤肉瘤分子生物学的最新进展:隆突性皮肤纤维肉瘤。
Curr Treat Options Oncol. 2019 Mar 14;20(4):29. doi: 10.1007/s11864-019-0628-3.
3
Outcome after surgical treatment of dermatofibrosarcoma protuberans: Is clinical follow-up always indicated?隆突性皮肤纤维肉瘤的手术治疗后结果:是否需要一直进行临床随访?
Cancer. 2019 Mar 1;125(5):735-741. doi: 10.1002/cncr.31924. Epub 2019 Jan 15.
4
Hormone receptors analysis in Chinese patients with dermatofibrosarcoma protuberans.中国隆突性皮肤纤维肉瘤患者的激素受体分析
J Surg Oncol. 2018 Jul;118(1):157-166. doi: 10.1002/jso.25117. Epub 2018 Jun 7.
5
Dermatofibrosarcoma Protuberans of Distal Extremities and Acral Sites: A Clinicopathologic Analysis of 27 Cases.远端肢体和肢端部位隆突性皮肤纤维肉瘤:27 例临床病理分析。
Am J Surg Pathol. 2018 Mar;42(3):413-419. doi: 10.1097/PAS.0000000000000998.
6
Dermatofibrosarcoma protuberans: pathology, genetics, and potential therapeutic strategies.隆突性皮肤纤维肉瘤:病理学、遗传学及潜在治疗策略
Ann Diagn Pathol. 2016 Dec;25:64-71. doi: 10.1016/j.anndiagpath.2016.09.013. Epub 2016 Sep 27.
7
Prognostic Factors, Treatment, and Survival in Dermatofibrosarcoma Protuberans.隆突性皮肤纤维肉瘤的预后因素、治疗和生存情况。
JAMA Dermatol. 2016 Dec 1;152(12):1365-1371. doi: 10.1001/jamadermatol.2016.1886.
8
Evolution of Dermatofibrosarcoma Protuberans to DFSP-Derived Fibrosarcoma: An Event Marked by Epithelial-Mesenchymal Transition-like Process and 22q Loss.隆突性皮肤纤维肉瘤向 DFSP 衍生纤维肉瘤的演进:具有上皮-间充质转化样过程和 22q 缺失的事件标志。
Mol Cancer Res. 2016 Sep;14(9):820-9. doi: 10.1158/1541-7786.MCR-16-0068. Epub 2016 Jun 2.
9
Clinicopathological features of dermatofibrosarcoma protuberans.隆突性皮肤纤维肉瘤的临床病理特征
Oncol Lett. 2016 Jan;11(1):661-667. doi: 10.3892/ol.2015.3966. Epub 2015 Nov 24.
10
Dermatofibrosarcoma protuberans: from translocation to targeted therapy.隆突性皮肤纤维肉瘤:从易位到靶向治疗。
Cancer Biol Med. 2015 Dec;12(4):375-84. doi: 10.7497/j.issn.2095-3941.2015.0067.