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脊柱尤因肉瘤的治疗理念与手术技术及文献综述

Philosophies And Surgical Techniques for Ewing's Sarcoma of Spine with Review of Literature.

作者信息

Sakhrekar Rajendra, Iorio Carlo, Yoon Samuel, Monjardino Maria Pia, Lewis Stephen, Gray Randolph

机构信息

Department of Spine Surgery, The Hospital for Sick Children, Toronto, Canada.

Children Hospital Westmead, Sydney, Australia.

出版信息

J Orthop Case Rep. 2024 Mar;14(3):168-175. doi: 10.13107/jocr.2024.v14.i03.4330.

Abstract

INTRODUCTION

Ewing sarcoma (ES) is a malignant and aggressive bony tumor affecting the most common age group of 5-20 years. It constitutes 10%-15% of all bone sarcomas and is the second most common primary malignant bone tumor after osteosarcoma. It usually presents with pain, which is typically constant and progressive in nature. The primary source of pain is due to the instability of the spine to support the weight of the body, the vertebral body's expanding cortices due to the growing mass, compression of nerve roots due to tumour mass, pathologic fractures, spinal cord compression, and invasion of tissue by the tumour mass.

METHODS

We reviewed the literature on Ewing's Sarcoma of the spine to evaluate its etiology, clinical presentations, differential diagnosis, imaging modalities and management with chemotherapy, radiotherapy, and surgical management. PubMed, EMBASE, Google Scholar and Cochrane key articles were searched. Keywords like 'Ewing's Sarcoma,' 'Spine,' 'etiology,' 'treatment,' 'surgical management,' and 'en bloc resection' were used.

DISCUSSION

The current management of Ewing's sarcoma of the spine usually involves three primary modalities: combination chemotherapy, surgery and/or radiotherapy. Recent improvements in combination chemotherapy (vincristine, doxorubicin, cyclophosphamide +/- Ifosfamide and etoposide) are among the most significant factors for improving survival. Also, recent advancements in radiotherapy, instrumentation, and fusion techniques in surgical management have been demonstrated to improve local disease control and overall survival.

CONCLUSION

Primary Ewing sarcoma of the spine is a rare condition affecting the most common age group of 5-20 years, accounting for 1-3 cases/million/year. About 5 % of cases have spine involvement. Recent improvements in combination chemotherapy have improved the overall survival rates. Enbloc resection and/or radiotherapy have improved local control of the disease.

摘要

引言

尤因肉瘤(ES)是一种恶性侵袭性骨肿瘤,好发于5至20岁这一最常见的年龄组。它占所有骨肉瘤的10% - 15%,是仅次于骨肉瘤的第二常见原发性恶性骨肿瘤。其通常表现为疼痛,这种疼痛一般持续且呈进行性。疼痛的主要原因包括脊柱难以支撑身体重量、由于肿瘤生长导致椎体皮质扩张、肿瘤肿块压迫神经根、病理性骨折、脊髓受压以及肿瘤肿块侵犯组织。

方法

我们回顾了关于脊柱尤因肉瘤的文献,以评估其病因、临床表现、鉴别诊断、影像学检查方法以及化疗、放疗和手术治疗。检索了PubMed、EMBASE、谷歌学术和Cochrane关键文章。使用了“尤因肉瘤”“脊柱”“病因”“治疗”“手术治疗”和“整块切除”等关键词。

讨论

目前脊柱尤因肉瘤的治疗通常涉及三种主要方式:联合化疗、手术和/或放疗。联合化疗(长春新碱、阿霉素、环磷酰胺+/-异环磷酰胺和依托泊苷)的近期进展是提高生存率的最重要因素之一。此外,手术治疗中放疗、器械和融合技术的近期进展已被证明可改善局部疾病控制和总体生存率。

结论

原发性脊柱尤因肉瘤是一种罕见疾病,好发于5至20岁这一最常见的年龄组,每年每百万人口中有1 - 3例。约5%的病例有脊柱受累。联合化疗的近期进展提高了总体生存率。整块切除和/或放疗改善了疾病的局部控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839d/10976549/27564e9833d4/JOCR-14-168-g001.jpg

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