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Recurrent epithelioid sarcoma in the thoracic spine successfully treated with multilevel total en bloc spondylectomy

机译:多层全脊椎全切除术成功治疗胸椎复发性上皮样肉瘤

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摘要

Epithelioid sarcoma (ES) is a rare type of soft tissue tumor. The common location of ES is at the extremities and rarely occurs in axial skeleton. Only two cases have been reported so far. Initial wide resection is recommended for the treatment of ES. However, the local recurrent rate is high and repeat surgical resection is still an option for the treatment of the recurrent. In the spine, however, the proper treatment of recurrent ES has not yet been published. Therefore, the objective of this case report is to illustrate the management strategies for the local recurrent ES after initial surgical resection in the thoracic spine. A 14-year-old boy was diagnosed for ES in the thoracic spine for 2 years. He was first treated by surgical resection followed by the chemotherapy and radiotherapy but the disease had progressed and the spine was gradually deformed. He was admitted to our facility with a large soft tissue mass, severe kyphotic deformity and neurological deficit. We removed the tumor en bloc by one-stage posterior only approach. The posterior transpedicular spinal instrumentation and fibular strut graft were used for the reconstruction. On the last follow-up, 2 year after the surgery, the patient remained in good condition. In conclusion, the recurrent ES of the spine can still archive a good oncological outcome with repeat radical resection, but the initial radical resection remains the best treatment option in order to retard the relentless course of this kind of malignancy.
机译:上皮样肉瘤(ES)是一种罕见的软组织肿瘤。 ES的共同部位在四肢,很少出现在轴向骨骼中。迄今为止,仅报道了两例。建议初次广泛切除治疗ES。但是,局部复发率很高,重复手术切除仍是复发治疗的一种选择。然而,在脊柱中,尚未见到复发性ES的正确治疗方法。因此,本病例报告的目的是说明胸椎初次手术切除后局部复发性ES的治疗策略。一名14岁男孩在胸椎被确诊为ES 2年。他首先接受外科手术切除,随后进行化学疗法和放疗,但病情已发展,脊柱逐渐变形。他因软组织肿大,严重的后凸畸形和神经功能缺损入院。我们通过一期仅后路手术切除了整个肿瘤。经椎弓根后路椎弓根内固定术和腓骨支撑移植物用于重建。在手术后2年的最后一次随访中,患者情况良好。总之,通过反复进行根治性切除术,脊柱复发性ES仍可取得良好的肿瘤学结局,但最初的根治性切除术仍是最好的治疗选择,以延缓这种恶性肿瘤的持续发展。

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