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[局限性软组织肉瘤]

[Localized soft tissue sarcomas].

作者信息

Hettler Madelaine, Jakob Jens

机构信息

Sektion Sarkomchirurgie, Chirurgische Klinik, Universitätsmedizin Mannheim, Medizinische Fakultät Mannheim der Universität Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Deutschland.

出版信息

Chirurgie (Heidelb). 2025 Jun;96(6):524-534. doi: 10.1007/s00104-025-02267-2. Epub 2025 Mar 19.

DOI:10.1007/s00104-025-02267-2
PMID:40105939
Abstract

Soft tissue sarcomas are rare malignant tumors originating from mesenchymal tissue. They are mostly located in the extremities, followed by the trunk and retroperitoneal regions. The group of soft tissue sarcomas comprises over 80 distinct histological subtypes, each with unique biological characteristics, with liposarcomas and leiomyosarcomas being the most frequent subtypes. In the clinical practice the algorithm from image, biopsy and (sarcoma) board has become established for the diagnostics of any soft tissue space-occupying lesion exceeding 3 cm in size. This enables the planning of a wide R0 resection, which can be defined as the standard for sarcoma surgery. For locally advanced and/or frequently metastasizing tumors, (neo)adjuvant radiotherapy and/or chemotherapy are usually indicated. Patients benefit from a sarcoma board to determine the treatment strategy. After treatment, clinical and radiological follow-ups should be conducted every 3-6 months, depending on the grade of the primary tumor.

摘要

软组织肉瘤是起源于间叶组织的罕见恶性肿瘤。它们大多位于四肢,其次是躯干和腹膜后区域。软组织肉瘤组包括80多种不同的组织学亚型,每种亚型都有独特的生物学特性,其中脂肪肉瘤和平滑肌肉瘤是最常见的亚型。在临床实践中,针对任何大小超过3厘米的软组织占位性病变,已确立了从影像学、活检到(肉瘤)多学科会诊的诊断流程。这有助于规划广泛的R0切除,可将其定义为肉瘤手术的标准。对于局部晚期和/或频繁转移的肿瘤,通常需要进行(新)辅助放疗和/或化疗。患者受益于肉瘤多学科会诊以确定治疗策略。治疗后,应根据原发肿瘤的分级每3至6个月进行临床和影像学随访。

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1
[Localized soft tissue sarcomas].[局限性软组织肉瘤]
Chirurgie (Heidelb). 2025 Jun;96(6):524-534. doi: 10.1007/s00104-025-02267-2. Epub 2025 Mar 19.
2
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Soft-tissue sarcoma.软组织肉瘤
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本文引用的文献

1
Ten recommendations for sarcoma surgery: consensus of the surgical societies based on the German S3 guideline "Adult Soft Tissue Sarcomas".肉瘤手术的 10 项建议:基于德国 S3 指南“成人软组织肉瘤”的外科协会共识。
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Cancer. 2020 Jan 1;126(9):1917-1928. doi: 10.1002/cncr.32735. Epub 2020 Feb 5.
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Development and external validation of a dynamic prognostic nomogram for primary extremity soft tissue sarcoma survivors.原发性肢体软组织肉瘤幸存者动态预后列线图的开发与外部验证
EClinicalMedicine. 2019 Nov 22;17:100215. doi: 10.1016/j.eclinm.2019.11.008. eCollection 2019 Dec.
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Screening populations at high risk for soft tissue sarcoma and surveillance following soft tissue sarcoma resection.软组织肉瘤高危人群筛查及软组织肉瘤切除术后监测。
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The impact of chemotherapy on survival of patients with extremity and trunk wall soft tissue sarcoma: revisiting the results of the EORTC-STBSG 62931 randomised trial.化疗对肢体和躯干壁软组织肉瘤患者生存的影响:重新审视 EORTC-STBSG 62931 随机试验的结果。
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Diagnostic accuracy of percutaneous biopsy in retroperitoneal sarcoma.腹膜后肉瘤经皮穿刺活检的诊断准确性。
Br J Surg. 2019 Mar;106(4):395-403. doi: 10.1002/bjs.11064. Epub 2019 Jan 24.
10
Soft tissue and visceral sarcomas: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up.软组织和内脏肉瘤:ESMO-EURACAN诊断、治疗及随访临床实践指南
Ann Oncol. 2018 Oct 1;29(Suppl 4):iv51-iv67. doi: 10.1093/annonc/mdy096.