Pleomorphic rhabdomyosarcoma infiltrating thoracic spine in a 59-year-old female patient: Case report.

IF 1 Q3 SURGERY
Matthias Spalteholz, Jens Gulow
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引用次数: 0

Abstract

Rhabdomyosarcoma (RMS) represents a malignant tumor of skeletal muscle cells arising from rhabdomyoblasts. RMS represents the most common soft tissue sarcoma in children. In adults it is uncommon and accounts for less than 1% of all malignant solid tumors. While treatment protocols are well known for children, there is no standardized regimen in adults. This is one reason, why the outcome in adults is worse than in children. We present the case of a 59-year-old female patient with pleomorphic rhabdomyosarcoma (PRMS) infiltrating the thoracic spine. Multimodality treatment was performed including en-bloc resection, adjuvant multidrug chemotherapy and radiation beam therapy. The patient was tumor free and had no relapse within 6 month follow-up.

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一名 59 岁女性患者的胸椎浸润性多形性横纹肌肉瘤:病例报告。
横纹肌肉瘤(RMS)是由横纹肌母细胞引起的骨骼肌细胞恶性肿瘤。横纹肌肉瘤是儿童最常见的软组织肉瘤。在成人中并不常见,占所有恶性实体瘤的比例不到 1%。虽然儿童的治疗方案众所周知,但成人却没有标准化的治疗方案。这也是为什么成人的治疗效果比儿童差的原因之一。我们介绍了一例 59 岁女性胸椎多形性横纹肌肉瘤(PRMS)患者的病例。患者接受了多模式治疗,包括全切、多药辅助化疗和放射治疗。患者在6个月的随访中无肿瘤且无复发。
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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