• 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

病例报告:青少年肋骨软骨肉瘤样恶性巨细胞瘤1例:诊断挑战与治疗

Case report: A rare case of chondrosarcoma-like malignant giant cell tumor in adolescent rib: diagnostic challenges and treatment.

作者信息

Qin Zhuolin, Li Longqian, Jing Tao, Wang Cheng

机构信息

The Second Clinical Medical College, Lanzhou University, Lanzhou, China.

Department of Thoracic Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.

出版信息

Front Oncol. 2025 Jan 15;14:1523104. doi: 10.3389/fonc.2024.1523104. eCollection 2024.

DOI:10.3389/fonc.2024.1523104
PMID:39882444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11774699/
Abstract

Chondrosarcoma-like malignant giant cell tumor (GCT) of the rib is an extremely rare and aggressive tumor, particularly in adolescents. This case report describes a 19-year-old female presenting with a GCT of the rib with chondrosarcomatous differentiation, highlighting the challenges posed by its unusual location and pathological complexity. Multidisciplinary diagnostic approaches, including advanced imaging, immunohistochemistry (IHC), and pathology, were essential for confirming the diagnosis. Key IHC markers such as Vimentin, SMA, and CD163, alongside genetic analysis excluding H3F3A mutations, guided the diagnostic process. The patient underwent successful surgical resection, achieving early recovery without adjuvant therapy. This report underscores the importance of early detection, precise pathological evaluation, and individualized surgical treatment for rare and high-risk tumors, emphasizing the need for long-term follow-up to monitor recurrence.

摘要

肋骨软骨肉瘤样恶性巨细胞瘤(GCT)极为罕见且具有侵袭性,在青少年中尤为如此。本病例报告描述了一名19岁女性,患有具有软骨肉瘤分化的肋骨GCT,凸显了其不寻常的位置和病理复杂性所带来的挑战。多学科诊断方法,包括先进的影像学检查、免疫组织化学(IHC)和病理学检查,对于确诊至关重要。关键的IHC标志物如波形蛋白、平滑肌肌动蛋白和CD163,以及排除H3F3A突变的基因分析,指导了诊断过程。患者接受了成功的手术切除,无需辅助治疗即可早期康复。本报告强调了早期发现、精确的病理评估和针对罕见高危肿瘤的个体化手术治疗的重要性,强调了长期随访以监测复发的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d8/11774699/83cc45ff98c0/fonc-14-1523104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d8/11774699/0e1dc301b4b8/fonc-14-1523104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d8/11774699/66914a2e67c0/fonc-14-1523104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d8/11774699/9c29ee4b5a25/fonc-14-1523104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d8/11774699/83cc45ff98c0/fonc-14-1523104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d8/11774699/0e1dc301b4b8/fonc-14-1523104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d8/11774699/66914a2e67c0/fonc-14-1523104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d8/11774699/9c29ee4b5a25/fonc-14-1523104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d8/11774699/83cc45ff98c0/fonc-14-1523104-g004.jpg

相似文献

1
Case report: A rare case of chondrosarcoma-like malignant giant cell tumor in adolescent rib: diagnostic challenges and treatment.病例报告:青少年肋骨软骨肉瘤样恶性巨细胞瘤1例:诊断挑战与治疗
Front Oncol. 2025 Jan 15;14:1523104. doi: 10.3389/fonc.2024.1523104. eCollection 2024.
2
Immunohistochemistry for histone H3G34W and H3K36M is highly specific for giant cell tumor of bone and chondroblastoma, respectively, in FNA and core needle biopsy.免疫组织化学染色检测 H3G34W 和 H3K36M 对 FNA 和核心针活检中的骨巨细胞瘤和软骨母细胞瘤具有高度特异性。
Cancer Cytopathol. 2018 Aug;126(8):552-566. doi: 10.1002/cncy.22000. Epub 2018 May 14.
3
Traumatic giant cell tumor of rib: A case report.创伤性肋骨巨细胞瘤:一例报告。
World J Clin Cases. 2022 Aug 26;10(24):8662-8666. doi: 10.12998/wjcc.v10.i24.8662.
4
Significance of Biogenetic Markers in Giant Cell Tumor Differentiation and Prognosis: A Narrative Review.生物遗传标志物在骨巨细胞瘤分化和预后中的意义:一项叙述性综述
Diagnostics (Basel). 2024 Dec 27;15(1):39. doi: 10.3390/diagnostics15010039.
5
The identification of H3F3A mutation in giant cell tumour of the clivus and the histological diagnostic algorithm of other clival lesions permit the differential diagnosis in this location.岩斜坡巨细胞瘤中 H3F3A 突变的鉴定和其他岩斜坡病变的组织学诊断算法可实现该部位的鉴别诊断。
BMC Cancer. 2018 Apr 2;18(1):358. doi: 10.1186/s12885-018-4291-z.
6
Malignant Giant Cell Tumor of Bone: A Clinicopathologic Series of 28 Cases Highlighting Genetic Differences Compared With Conventional, Atypical, and Metastasizing Conventional Tumors.骨恶性巨细胞瘤:28例临床病理系列研究,突出与传统、非典型及转移性传统肿瘤相比的基因差异
Am J Surg Pathol. 2025 Jun 1;49(6):539-553. doi: 10.1097/PAS.0000000000002387. Epub 2025 Mar 13.
7
H3F3A G34 mutation DNA sequencing and G34W immunohistochemistry analysis in 366 cases of giant cell tumors of bone and other bone tumors.在 366 例骨巨细胞瘤和其他骨肿瘤中进行 H3F3A G34 突变 DNA 测序和 G34W 免疫组织化学分析。
Histol Histopathol. 2021 Jan;36(1):61-68. doi: 10.14670/HH-18-264. Epub 2020 Sep 4.
8
Recurrent primary mediastinal giant cell tumor of soft tissue with radiological findings: a rare case report and literature review.复发性原发性纵隔巨大软组织细胞瘤的影像学表现:一例罕见病例报告及文献复习。
World J Surg Oncol. 2017 Jul 26;15(1):137. doi: 10.1186/s12957-017-1205-5.
9
Giant cell tumor of soft tissue of the breast: Case report with H3F3A mutation analysis and review of the literature.乳腺软组织巨细胞瘤:H3F3A 突变分析病例报告及文献复习。
Pathol Res Pract. 2020 Feb;216(2):152750. doi: 10.1016/j.prp.2019.152750. Epub 2019 Nov 19.
10
Primary Giant Cell Tumor of the Breast With Pulmonary Metastasis: A Case Report and Review of the Literature.乳腺原发性巨细胞瘤伴肺转移:一例报告及文献复习
Front Oncol. 2021 Nov 5;11:638237. doi: 10.3389/fonc.2021.638237. eCollection 2021.

本文引用的文献

1
TP53 mutations in myeloid neoplasms: implications for accurate laboratory detection, diagnosis, and treatment.髓系肿瘤中 TP53 基因突变:对准确的实验室检测、诊断和治疗的影响。
Lab Med. 2024 Nov 4;55(6):686-699. doi: 10.1093/labmed/lmae048.
2
An optimized postsurgery follow-up strategy for patients with esophageal cancer: a cohort study.一项针对食管癌患者的优化术后随访策略:队列研究
Int J Surg. 2024 Jan 1;110(1):332-341. doi: 10.1097/JS9.0000000000000827.
3
Giant Cell Tumor and Giant Cell Reparative Granuloma of Bone of the Head: CT and MR Imaging Findings.
骨巨细胞瘤和骨巨细胞修复性肉芽肿的头部:CT 和 MR 成像表现。
Comb Chem High Throughput Screen. 2023;26(6):1180-1185. doi: 10.2174/1386207325666220818124912.
4
Long-term follow-up of nilotinib in patients with advanced tenosynovial giant cell tumours: Long-term follow-up of nilotinib in TGCT.尼洛替尼治疗晚期腱膜性巨细胞瘤患者的长期随访:尼洛替尼治疗 TGCT 的长期随访。
Eur J Cancer. 2022 Sep;173:219-228. doi: 10.1016/j.ejca.2022.06.028. Epub 2022 Aug 3.
5
Denosumab in Giant Cell Tumor of Bone: Multidisciplinary Medical Management Based on Pathophysiological Mechanisms and Real-World Evidence.地诺单抗治疗骨巨细胞瘤:基于病理生理机制和真实世界证据的多学科医学管理
Cancers (Basel). 2022 May 4;14(9):2290. doi: 10.3390/cancers14092290.
6
A Rationale for the Activity of Bone Target Therapy and Tyrosine Kinase Inhibitor Combination in Giant Cell Tumor of Bone and Desmoplastic Fibroma: Translational Evidences.骨靶向治疗与酪氨酸激酶抑制剂联合应用于骨巨细胞瘤和促纤维组织增生性纤维瘤的作用原理:转化医学证据
Biomedicines. 2022 Feb 3;10(2):372. doi: 10.3390/biomedicines10020372.
7
Giant Cell Tumor of Bone: An Update.骨巨细胞瘤:最新进展。
Curr Oncol Rep. 2021 Mar 22;23(5):51. doi: 10.1007/s11912-021-01047-5.
8
Denosumab treatment for giant-cell tumor of bone: a systematic review of the literature.地舒单抗治疗骨巨细胞瘤:文献系统评价。
Arch Orthop Trauma Surg. 2019 Oct;139(10):1339-1349. doi: 10.1007/s00402-019-03167-x. Epub 2019 Mar 15.
9
Genomic and transcriptomic characterisation of undifferentiated pleomorphic sarcoma of bone.骨未分化多形性肉瘤的基因组和转录组特征。
J Pathol. 2019 Feb;247(2):166-176. doi: 10.1002/path.5176. Epub 2018 Dec 27.
10
Giant cell tumor of bone: updated molecular pathogenesis and tumor biology.骨巨细胞瘤:最新的分子发病机制和肿瘤生物学。
Hum Pathol. 2018 Nov;81:1-8. doi: 10.1016/j.humpath.2018.06.017. Epub 2018 Jun 23.