Linhart Camilla, MacLeod Craig
Doctor of Medicine (MD) University of Notre Dame Australia (Sydney Campus), Darlinghurst, New South Wales 2010, Australia.
Border Medical Oncology GenesisCare Albury Wodonga Regional Cancer Centre, Albury, New South Wales 2640, Australia.
Case Rep Oncol Med. 2024 Aug 27;2024:5782352. doi: 10.1155/2024/5782352. eCollection 2024.
This study examines a unique case of a 61-year-old male with a 5-year history of a progressively growing mass above his right shoulder, diagnosed as a dedifferentiated pleomorphic liposarcoma. Using computerized tomography-guided core needle biopsy, the tumour was identified as intermediate to high grade. Surgical removal required preoperative radiotherapy to reduce the size of the tumour. Several unique characteristics set apart this particular case of liposarcoma: its substantial size, its unpredictable growth pattern, its absence of metastasis, and notably, its prolonged period of being untreated. This case report outlines the clinical background, diagnostic procedures, and treatment modalities employed in managing this condition, emphasizing a localized dual therapy approach combining radiotherapy and surgery. Emphasis is placed on distinguishing liposarcoma from lipoblastoma, a benign adipocyte tumour, to facilitate accurate diagnosis and appropriate treatment selection. The positive result achieved in this case could provide valuable insights for the future treatment and management of similarly sized aggressive tumours.
本研究考察了一例独特病例,患者为一名61岁男性,其右肩部上方有一逐渐增大的肿块,病史长达5年,诊断为去分化多形性脂肪肉瘤。通过计算机断层扫描引导下的粗针活检,该肿瘤被确定为中高级别。手术切除需要术前放疗以缩小肿瘤大小。该例脂肪肉瘤有几个独特特征:体积巨大、生长模式不可预测、无转移,尤其值得注意的是,其长时间未接受治疗。本病例报告概述了该病例的临床背景、诊断程序及治疗方式,强调了采用放疗和手术相结合的局部双重治疗方法。重点在于将脂肪肉瘤与脂肪母细胞瘤(一种良性脂肪细胞肿瘤)区分开来,以促进准确诊断和恰当的治疗选择。该病例取得的阳性结果可为未来治疗和管理类似大小的侵袭性肿瘤提供宝贵见解。