四肢软组织肉瘤综合治疗术后骨折。

Q2 Medicine Sarcoma Pub Date : 2021-03-15 eCollection Date: 2021-01-01 DOI:10.1155/2021/8877567
Meredith K Bartelstein, Divya Yerramilli, Alexander B Christ, Shachar Kenan, Koichi Ogura, Tomohiro Fujiwara, Nicola Fabbri, John H Healey
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引用次数: 5

摘要

肢体软组织肉瘤(STS)的治疗通常采用保肢手术和放射治疗;采用这种处理方法,可以实现较高的局部控制率。然而,放射后骨折,即在先前的放射领域发生的骨折,创伤很小或没有创伤,是一种严重的晚期并发症,发生在2-22%接受STS手术和放射治疗的患者中。放疗后持续骨折存在多种危险因素,包括高辐射剂量、女性、骨膜剥离、老年、股骨位置和化疗。这些病理性骨折的治疗可能很困难,并发症包括延迟愈合、不愈合和感染,这些都是特别的挑战。在这里,我们回顾了与STS患者放射后骨折相关的机制、危险因素和治疗挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Postradiation Fractures after Combined Modality Treatment in Extremity Soft Tissue Sarcomas.

Soft tissue sarcoma (STS) of the extremities is typically treated with limb-sparing surgery and radiation therapy; with this treatment approach, high local control rates can be achieved. However, postradiation bone fractures, fractures occurring in the prior radiation field with minimal or no trauma, are a serious late complication that occurs in 2-22% of patients who receive surgery and radiation for STS. Multiple risk factors for sustaining a postradiation fracture exist, including high radiation dose, female sex, periosteal stripping, older age, femur location, and chemotherapy administration. The treatment of these pathological fractures can be difficult, with complications including delayed union, nonunion, and infection posing particular challenges. Here, we review the mechanisms, risk factors, and treatment challenges associated with postradiation fractures in STS patients.

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来源期刊
Sarcoma
Sarcoma Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.00
自引率
0.00%
发文量
15
审稿时长
14 weeks
期刊介绍: Sarcoma is dedicated to publishing papers covering all aspects of connective tissue oncology research. It brings together work from scientists and clinicians carrying out a broad range of research in this field, including the basic sciences, molecular biology and pathology and the clinical sciences of epidemiology, surgery, radiotherapy and chemotherapy. High-quality papers concerning the entire range of bone and soft tissue sarcomas in both adults and children, including Kaposi"s sarcoma, are published as well as preclinical and animal studies. This journal provides a central forum for the description of advances in diagnosis, assessment and treatment of this rarely seen, but often mismanaged, group of patients.
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