• 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

成人腰椎原发性间叶性软骨肉瘤:一例报告并文献复习

Primary mesenchymal chondrosarcoma of the adult lumbar spine: a case report and review of the literature.

作者信息

Lin Maoqiang, Zhou Haiyu, Zhang Xiaobo, Hu Yicun, Guo Taowen, Shi Jintao

机构信息

Department of Orthopedics, Lanzhou University Second Hospital, Lanzhou, China.

Key Laboratory of Bone and Joint Disease Research of Gansu Province, Lanzhou, China.

出版信息

Transl Cancer Res. 2022 Sep;11(9):3363-3370. doi: 10.21037/tcr-22-122.

DOI:10.21037/tcr-22-122
PMID:36237229
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9552263/
Abstract

BACKGROUND

Primary mesenchymal chondrosarcoma (PMC) is a relatively rare malignancy that can occur in bone or soft tissue, but rarely in the lumbar spine; there is currently no unified treatment. We report a case of mesenchymal chondrosarcoma originating from the L1 vertebra.

CASE DESCRIPTION

A 47-year-old female patient was admitted to the hospital with intermittent low back pain for 20 years, accompanied by intermittent headache and radiating pain in both lower limbs. After admission, magnetic resonance imaging (MRI) showed bone destruction of the L1 vertebral body and accessories and a surrounding soft tissue mass. Enhanced MRI revealed significant enhancement of the L1 vertebral body and soft tissue mass. Technetium 99 m-methylene diphosphonate (99 m Tc-MDP) bone scan showed abnormally high metabolism in the L1 vertebral body, which is highly suspicious of malignancy, and vertebral biopsy revealed a soft tissue malignancy originating from the mesenchymal tissue. Total vertebrectomy combined with postoperative adjuvant radiotherapy was planned, but the patient refused radiotherapy for financial reasons. Intraoperative frozen sections indicated mesenchymal chondrosarcoma, as confirmed by postoperative pathological examination. After 1 year of outpatient follow-up, the patient had no related symptoms, and normal motor and sensory function, and her condition had improved.

CONCLUSIONS

Total tumor resection is an effective treatment for PMC, and increased attention to this disease in the clinic is essential.

摘要

背景

原发性间叶性软骨肉瘤(PMC)是一种相对罕见的恶性肿瘤,可发生于骨或软组织,但很少发生于腰椎;目前尚无统一的治疗方法。我们报告一例起源于L1椎体的间叶性软骨肉瘤病例。

病例描述

一名47岁女性患者因间歇性腰痛20年入院,伴有间歇性头痛及双下肢放射性疼痛。入院后,磁共振成像(MRI)显示L1椎体及附件骨质破坏,周围有软组织肿块。增强MRI显示L1椎体及软组织肿块明显强化。锝99m-亚甲基二膦酸盐(99mTc-MDP)骨扫描显示L1椎体代谢异常增高,高度怀疑为恶性肿瘤,椎体活检显示为起源于间叶组织的软组织恶性肿瘤。计划行全椎体切除术并术后辅助放疗,但患者因经济原因拒绝放疗。术中冰冻切片提示为间叶性软骨肉瘤,术后病理检查确诊。门诊随访1年后,患者无相关症状,运动及感觉功能正常,病情好转。

结论

肿瘤全切是治疗PMC的有效方法,临床对此病增加关注至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/fd11375bf60f/tcr-11-09-3363-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/75b9e28f9561/tcr-11-09-3363-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/ada8190e28fe/tcr-11-09-3363-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/8139ee425fda/tcr-11-09-3363-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/a1b2c02deb63/tcr-11-09-3363-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/fd11375bf60f/tcr-11-09-3363-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/75b9e28f9561/tcr-11-09-3363-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/ada8190e28fe/tcr-11-09-3363-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/8139ee425fda/tcr-11-09-3363-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/a1b2c02deb63/tcr-11-09-3363-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c4/9552263/fd11375bf60f/tcr-11-09-3363-f5.jpg

相似文献

1
Primary mesenchymal chondrosarcoma of the adult lumbar spine: a case report and review of the literature.成人腰椎原发性间叶性软骨肉瘤:一例报告并文献复习
Transl Cancer Res. 2022 Sep;11(9):3363-3370. doi: 10.21037/tcr-22-122.
2
Primary intraspinal dumbbell-shaped mesenchymal chondrosarcoma with massive calcifications: a case report and review of the literature.原发性椎管内哑铃形间充质软骨肉瘤伴大量钙化:病例报告及文献复习
World J Surg Oncol. 2016 Aug 3;14(1):203. doi: 10.1186/s12957-016-0963-9.
3
Surgical treatment of metastatic mesenchymal chondrosarcoma to the spine: A case report.脊柱转移性间叶性软骨肉瘤的外科治疗:一例报告
Medicine (Baltimore). 2020 Jan;99(5):e18643. doi: 10.1097/MD.0000000000018643.
4
Rare malignant primary spinal intradural extramedullary mesenchymal chondrosarcoma: a case report and literature review.罕见的原发性脊髓硬膜内髓外间叶性软骨肉瘤:一例报告及文献复习
Transl Cancer Res. 2022 Sep;11(9):3371-3378. doi: 10.21037/tcr-21-2703.
5
Mesenchymal chondrosarcoma treated with total en bloc spondylectomy for 2 consecutive lumbar vertebrae resulted in continuous disease-free survival for more than 5 years: case report.连续两节腰椎整块切除治疗间叶性软骨肉瘤,实现了超过5年的持续无病生存:病例报告
Spine (Phila Pa 1976). 2006 Apr 15;31(8):E231-6. doi: 10.1097/01.brs.0000210297.02677.66.
6
Spinal mesenchymal chondrosarcoma: A case report of a rare malignant tumor.脊柱间叶性软骨肉瘤:一例罕见恶性肿瘤的病例报告
Surg Neurol Int. 2023 Apr 7;14:128. doi: 10.25259/SNI_206_2023. eCollection 2023.
7
Cervical subtotal en-bloc spondylectomy of C6 mesenchymal chondrosarcoma.C6间叶性软骨肉瘤的颈椎次全整块椎体切除术。
Eur Spine J. 2016 Jul;25(7):2117-23. doi: 10.1007/s00586-015-4297-z. Epub 2015 Nov 10.
8
Case report: Mesenchymal chondrosarcoma of the lumbar spine in a child.病例报告:儿童腰椎间叶性软骨肉瘤。
Clin Orthop Relat Res. 2010 Aug;468(8):2288-94. doi: 10.1007/s11999-010-1297-5. Epub 2010 Mar 19.
9
Diagnosis and surgical treatment of primary isolated aggressive lumbar myeloid sarcoma: a rare case report and review of the literatures.原发性孤立性侵袭性腰椎髓外浆细胞瘤的诊断和外科治疗:一例罕见病例报告并文献复习。
BMC Musculoskelet Disord. 2021 Feb 24;22(1):220. doi: 10.1186/s12891-021-04066-2.
10
Vertebral body chondrosarcoma with metastasis to the scalp.椎体软骨肉瘤伴头皮转移。
BJR Case Rep. 2018 Jul 12;5(1):20180037. doi: 10.1259/bjrcr.20180037. eCollection 2019 Feb.

引用本文的文献

1
Aggressive Mesenchymal Chondrosarcoma of the Rib With Early Skeletal Metastases: A Diagnostic Challenge.伴有早期骨转移的肋骨侵袭性间叶性软骨肉瘤:一项诊断挑战。
Cureus. 2024 Nov 15;16(11):e73718. doi: 10.7759/cureus.73718. eCollection 2024 Nov.
2
Mesenchymal Chondrosarcoma from Diagnosis to Clinical Trials.从诊断到临床试验的间充质软骨肉瘤
Cancers (Basel). 2023 Sep 15;15(18):4581. doi: 10.3390/cancers15184581.
3
Brief overview of primary mesenchymal chondrosarcoma and discussion of a case report.原发性间叶性软骨肉瘤概述及一例病例报告讨论

本文引用的文献

1
Surgical treatment of metastatic mesenchymal chondrosarcoma to the spine: A case report.脊柱转移性间叶性软骨肉瘤的外科治疗:一例报告
Medicine (Baltimore). 2020 Jan;99(5):e18643. doi: 10.1097/MD.0000000000018643.
2
Vertebral body chondrosarcoma with metastasis to the scalp.椎体软骨肉瘤伴头皮转移。
BJR Case Rep. 2018 Jul 12;5(1):20180037. doi: 10.1259/bjrcr.20180037. eCollection 2019 Feb.
3
Primary intraspinal dumbbell-shaped mesenchymal chondrosarcoma with massive calcifications: a case report and review of the literature.
Transl Cancer Res. 2022 Dec;11(12):4235-4236. doi: 10.21037/tcr-22-2284.
原发性椎管内哑铃形间充质软骨肉瘤伴大量钙化:病例报告及文献复习
World J Surg Oncol. 2016 Aug 3;14(1):203. doi: 10.1186/s12957-016-0963-9.
4
Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics.STAT6 的核表达可将孤立性纤维性肿瘤与组织学模拟物区分开来。
Mod Pathol. 2014 Mar;27(3):390-5. doi: 10.1038/modpathol.2013.164. Epub 2013 Sep 13.
5
Radiation therapy is associated with fewer recurrences in mesenchymal chondrosarcoma.放疗与间叶性软骨肉瘤的复发率降低有关。
Clin Orthop Relat Res. 2014 Mar;472(3):856-64. doi: 10.1007/s11999-013-3064-x.
6
Case report: Mesenchymal chondrosarcoma of the lumbar spine in a child.病例报告:儿童腰椎间叶性软骨肉瘤。
Clin Orthop Relat Res. 2010 Aug;468(8):2288-94. doi: 10.1007/s11999-010-1297-5. Epub 2010 Mar 19.
7
Mesenchymal chondrosarcoma of soft tissues and bone in children, adolescents, and young adults: experiences of the CWS and COSS study groups.儿童、青少年及青年软组织和骨的间叶性软骨肉瘤:CWS和COSS研究组的经验
Cancer. 2008 Jun;112(11):2424-31. doi: 10.1002/cncr.23457.
8
Mesenchymal chondrosarcoma treated with total en bloc spondylectomy for 2 consecutive lumbar vertebrae resulted in continuous disease-free survival for more than 5 years: case report.连续两节腰椎整块切除治疗间叶性软骨肉瘤,实现了超过5年的持续无病生存:病例报告
Spine (Phila Pa 1976). 2006 Apr 15;31(8):E231-6. doi: 10.1097/01.brs.0000210297.02677.66.
9
Unusual benign and malignant chondroid tumors of bone. A survey of some mesenchymal cartilage tumors and malignant chondroblastic tumors, including a few multicentric ones, as well as many atypical benign chondroblastomas and chondromyxoid fibromas.骨的罕见良性和恶性软骨样肿瘤。对一些间叶性软骨肿瘤和恶性成软骨细胞瘤的调查,包括少数多中心性肿瘤,以及许多非典型良性成软骨细胞瘤和软骨黏液样纤维瘤。
Cancer. 1959 Nov-Dec;12:1142-57. doi: 10.1002/1097-0142(195911/12)12:6<1142::aid-cncr2820120610>3.0.co;2-d.
10
Prognostic factors and outcome of pelvic, sacral, and spinal chondrosarcomas: a center-based study of 69 cases.骨盆、骶骨和脊柱软骨肉瘤的预后因素及结果:一项基于中心的69例病例研究
Cancer. 2001 Apr 1;91(7):1201-12. doi: 10.1002/1097-0142(20010401)91:7<1201::aid-cncr1120>3.0.co;2-w.