胸壁多形性肉瘤1例

Sonali Parida, Srinibash Sahoo
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引用次数: 0

摘要

摘要原发性胸壁多形性脂肪肉瘤是一种罕见的肿瘤。大多数报道的胸壁脂肪肉瘤是低级别、高分化的纵隔延伸。大多数是由皮下脂肪瘤发展而来。完全手术切除是首选的治疗方式。辅助放疗或放化疗对这些肿瘤的益处是一个有争议的话题。我们报告一例罕见的高级别原发性多形性脂肪肉瘤,患者为50岁男性,表现为胸壁前壁疼痛性肿胀,并延伸至胸膜,但无纵隔受累或远处转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pleomorphic sarcoma of the chest wall: A case report
Primary pleomorphic liposarcoma of the chest wall is a rare entity. Most of the reported cases of the chest wall liposarcomas are low grade, well differentiated with mediastinal extension. Majority of these develop from a subcutaneous lipoma. Complete surgical resection is the preferred treatment modality. The benefit of adjuvant radiotherapy or chemoradiotherapy for these tumors is a subject of debate. We report, an unusual case of high grade primary pleomorphic subtype of liposarcoma in a 50-year-old male presenting with a painful swelling in the anterior thoracic wall extending into the pleura but without any mediastinal involvement or distant metastasis.
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