• 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

19号染色体短臂标记染色体与恶性纤维组织细胞瘤的复发相关。

19p+ marker chromosome correlates with relapse in malignant fibrous histiocytoma.

作者信息

Choong P F, Mandahl N, Mertens F, Willén H, Alvegård T, Kreicbergs A, Mitelman F, Rydholm A

机构信息

Department of Orthopedics, University Hospital, Lund, Sweden.

出版信息

Genes Chromosomes Cancer. 1996 Jun;16(2):88-93. doi: 10.1002/(SICI)1098-2264(199606)16:2<88::AID-GCC2>3.0.CO;2-Z.

DOI:10.1002/(SICI)1098-2264(199606)16:2<88::AID-GCC2>3.0.CO;2-Z
PMID:8818655
Abstract

In this study, we examined the relationship of 19p13 aberrations, usually leading to addition of unknown material (19p+), and ring chromosomes to clinical outcome in patients with malignant fibrous histiocytoma (MFH). Analysis of 69 MFHs revealed 19 tumors with 19p+ and 24 tumors with ring chromosomes. After a median follow-up period of 36 months, 24 patients developed metastases, and 27 patients developed local recurrences. Ten patients had both local recurrences and metastases. Local recurrence was more common in association with 19p+ than without. Metastasis was more common with 19p+ tumors in high-risk patients (tumor size > 5 cm and grade III-IV; n = 48) than those without 19p+. There was a trend suggesting fewer relapses after tumors with ring chromosomes. 19p+ may be an independent marker of unfavorable outcome in MFH.

摘要

在本研究中,我们检测了19号染色体短臂1区3带(19p13)异常(通常导致未知物质附加,即19p+)以及环状染色体与恶性纤维组织细胞瘤(MFH)患者临床预后的关系。对69例MFH进行分析,发现19例存在19p+,24例存在环状染色体。中位随访期为36个月后,24例患者发生转移,27例患者出现局部复发。10例患者既有局部复发又有转移。19p+相关的局部复发比无19p+的情况更常见。在高危患者(肿瘤大小>5 cm且分级为III-IV级;n = 48)中,19p+肿瘤发生转移比无19p+肿瘤更常见。有一个趋势表明,环状染色体肿瘤后的复发较少。19p+可能是MFH不良预后的一个独立标志物。

相似文献

1
19p+ marker chromosome correlates with relapse in malignant fibrous histiocytoma.19号染色体短臂标记染色体与恶性纤维组织细胞瘤的复发相关。
Genes Chromosomes Cancer. 1996 Jun;16(2):88-93. doi: 10.1002/(SICI)1098-2264(199606)16:2<88::AID-GCC2>3.0.CO;2-Z.
2
Malignant fibrous histiocytomas with a 19p+ marker chromosome have increased relapse rate.具有19号染色体短臂增加标记的恶性纤维组织细胞瘤复发率升高。
Genes Chromosomes Cancer. 1990 Nov;2(4):296-9. doi: 10.1002/gcc.2870020407.
3
Time dependence of prognostic factors for patients with soft tissue sarcoma: a Scandinavian Sarcoma Group Study of 338 malignant fibrous histiocytomas.软组织肉瘤患者预后因素的时间依赖性:斯堪的纳维亚肉瘤研究组对338例恶性纤维组织细胞瘤的研究
Cancer. 2004 May 15;100(10):2233-9. doi: 10.1002/cncr.20254.
4
[A comparison of malignant fibrous histiocytoma of head, neck and extremities].头颈部与四肢恶性纤维组织细胞瘤的比较
Chin Med J (Engl). 2000 Jun;113(6):532-5.
5
Comparative genomic hybridization of malignant fibrous histiocytoma reveals a novel prognostic marker.恶性纤维组织细胞瘤的比较基因组杂交揭示了一种新的预后标志物。
Am J Pathol. 1997 Oct;151(4):1153-61.
6
[Malignant fibrous histiocytoma of the maxillofacial region].[颌面部恶性纤维组织细胞瘤]
Dtsch Z Mund Kiefer Gesichtschir. 1991 May-Jun;15(3):165-9.
7
[Malignant fibrous histiocytoma of head and neck: clinical analysis of 21 cases].[头颈部恶性纤维组织细胞瘤:21例临床分析]
Ai Zheng. 2003 May;22(5):523-5.
8
Malignant fibrous histiocytoma and other fibrohistiocytic tumors in pediatric patients: the St. Jude Children's Research Hospital experience.小儿恶性纤维组织细胞瘤及其他纤维组织细胞性肿瘤:圣裘德儿童研究医院的经验
Cancer. 2003 Jun 1;97(11):2839-47. doi: 10.1002/cncr.11384.
9
Angiomatoid malignant fibrous histiocytoma. A follow-up study of 108 cases with evaluation of possible histologic predictors of outcome.血管样恶性纤维组织细胞瘤。108例随访研究及对可能的组织学预后预测因素的评估。
Am J Surg Pathol. 1990 Dec;14(12):1126-32.
10
Retroperitoneal liposarcomas: follow-up analysis of dedifferentiation after clinicopathologic reexamination of 86 liposarcomas and malignant fibrous histiocytomas.腹膜后脂肪肉瘤:对86例脂肪肉瘤和恶性纤维组织细胞瘤进行临床病理复查后对去分化的随访分析
Cancer. 2006 Jun 15;106(12):2725-33. doi: 10.1002/cncr.21933.

引用本文的文献

1
Current research and management of undifferentiated pleomorphic sarcoma/myofibrosarcoma.未分化多形性肉瘤/肌纤维肉瘤的当前研究与管理
Front Genet. 2023 Feb 16;14:1109491. doi: 10.3389/fgene.2023.1109491. eCollection 2023.
2
Metachronous Malignant Fibrous HistiocytomaA Rare Case Report.异时性恶性纤维组织细胞瘤:一例罕见病例报告
Iran J Pathol. 2018 Fall;13(4):474-478. Epub 2018 Sep 25.
3
Proposal for Modification of Cahan's Criteria Utilizing Molecular Genetic Analyses for Cases without Baseline Histopathology: A Unique Method Applicable to Primary Radiosurgery.
利用分子遗传学分析对无基线组织病理学的病例修改卡汉标准的建议:一种适用于原发性放射外科的独特方法。
J Neurol Surg B Skull Base. 2019 Feb;80(1):10-17. doi: 10.1055/s-0038-1655759. Epub 2018 May 31.
4
Characterization and Drug Sensitivity of a New High-Grade Myxofibrosarcoma Cell Line.一种新型高级别黏液纤维肉瘤细胞系的特征及药敏性
Cells. 2018 Oct 25;7(11):186. doi: 10.3390/cells7110186.
5
Characterization of the new human pleomorphic undifferentiated sarcoma TP53-null cell line mfh-val2.新型人多形性未分化肉瘤TP53缺失细胞系mfh-val2的特性分析
Cytotechnology. 2017 Aug;69(4):539-550. doi: 10.1007/s10616-017-0112-5. Epub 2017 Jul 4.
6
Sarcomas of the heart as a difficult interdisciplinary problem.心脏肉瘤作为一个困难的跨学科问题。
Arch Med Sci. 2014 Feb 24;10(1):135-48. doi: 10.5114/aoms.2014.40741. Epub 2014 Feb 23.
7
Establishment of a new human pleomorphic malignant fibrous histiocytoma cell line, FU-MFH-2: molecular cytogenetic characterization by multicolor fluorescence in situ hybridization and comparative genomic hybridization.建立一株新型人多形性恶性纤维组织细胞瘤细胞系 FU-MFH-2:多色荧光原位杂交和比较基因组杂交的分子细胞遗传学特征。
J Exp Clin Cancer Res. 2010 Nov 24;29(1):153. doi: 10.1186/1756-9966-29-153.
8
Myxoid malignant fibrous histiocytoma with multiple primary sites.具有多个原发部位的黏液样恶性纤维组织细胞瘤
Sarcoma. 2002;6(1):51-5. doi: 10.1080/13577140220127567.
9
Gain of 17q in malignant fibrous histiocytoma is associated with a longer disease-free survival and a low risk of developing distant metastasis.恶性纤维组织细胞瘤中17号染色体长臂的增加与较长的无病生存期和远处转移低风险相关。
Br J Cancer. 2003 Aug 18;89(4):720-6. doi: 10.1038/sj.bjc.6601069.
10
Comparative genomic hybridization of malignant fibrous histiocytoma reveals a novel prognostic marker.恶性纤维组织细胞瘤的比较基因组杂交揭示了一种新的预后标志物。
Am J Pathol. 1997 Oct;151(4):1153-61.