Is primary thoracic ewing sarcoma aggressive than others? seventeenyears' experience

Seray Hazer, G. Fındık, K. Aydoğdu, Y. Ağaçkıran, S. Gülhan, M. Demiröz, Pınar Bıçakçıoğlu, S. Kaya
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引用次数: 1

Abstract

Background: Ewing sarcoma (ES) is an uncommon aggressive malignant tumor of the bone and/or soft tissue and belongs to peripheral primitive neuroectodermal tumor (PNET) family of tumors. Bone PNETs primarily arise from the diaphysis of long bones, where as soft tissue PNETs are most commonly found in the chest wall. Multidisciplinary treatments, including chemotherapy, surgery, radiotherapy, or all three combined, improve the survival of patients with localized ES. However, the best approach to achieve local control remains controversial. Materials and Methods: We retrospectively analysed the medical records and pathology data of 14 patients (8 male, 6 female; mean age, 23.2 [range, 4-54] years) with primary thoracic ES who underwent surgery in our clinic between January 2002 and December 2019. In addition, the treatment modalities and tumor-related factors of chest wall ES and lung parenchyma were evaluated. Results: The most frequent complaint was chest pain (n = 7). In 10 patients, the tumor originated from the ribs, whereas the remaining 4 patients had lung parenchymal tumors. Ten patients underwent complete tumor excision with chest wall resection, one patient underwent lower lobectomy with chest wall resection, and three patients underwent complete tumor excision via wedge resection. All patients were treated with chemotherapy, except two who underwent bone marrow transplantation. The median follow-up was 31.6 (range, 2-84) months. Relapses were seen in 5 cases in the median 19.8th (range, 4-60) month. Conclusions: Complete tumor resection is the most effective treatment for thoracic ES and multimodal therapy (surgical resection, chemotherapy, and local radiation therapy), which is recommended when indicated, constitutes the optimal treatment for ES. Although relapses occur within the early postoperative period, late relapses are not uncommon. The follow-up periods must be short and should be maintained long term for late relapses.
原发性胸翼肉瘤是否具有侵袭性?seventeenyears的经验
背景:尤文氏肉瘤(Ewing sarcoma, ES)是一种罕见的骨和/或软组织侵袭性恶性肿瘤,属于外周原始神经外胚层肿瘤(PNET)家族。骨PNETs主要来自长骨骨干,而软组织PNETs最常见于胸壁。多学科治疗,包括化疗、手术、放疗,或三者联合,可提高局限性ES患者的生存率。然而,实现局部控制的最佳方法仍然存在争议。材料与方法:回顾性分析14例患者的病历及病理资料(男8例,女6例;2002年1月至2019年12月在我院接受手术的原发性胸椎ES患者平均年龄23.2岁(范围4-54岁)。同时对胸壁ES及肺实质的治疗方式及肿瘤相关因素进行评价。结果:最常见的主诉是胸痛(n = 7),其中10例肿瘤起源于肋骨,其余4例为肺实质肿瘤。10例患者行肿瘤全切胸壁切除术,1例患者行下肺叶全切胸壁切除术,3例患者行楔形全切。除2例接受骨髓移植外,所有患者均接受化疗。中位随访时间为31.6个月(范围2-84)。5例复发中位时间为19.8个月(范围4-60个月)。结论:肿瘤完全切除是胸部ES最有效的治疗方法,多模式治疗(手术切除、化疗和局部放疗)是ES的最佳治疗方法。虽然复发发生在术后早期,但晚期复发并不罕见。随访时间必须短,对于晚期复发应保持长期随访。
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