Pleomorphic Liposarcoma of Femur: A Rare Soft Tissue Sarcoma Metastasized to the Bone—Case Report and Review of Literature

IF 0.4 Q4 ORTHOPEDICS Case Reports in Orthopedics Pub Date : 2022-03-07 DOI:10.1155/2022/9195529
Thanate Poosiripinyo, Thanapon Chobpenthai, T. Wisanuyotin, W. Sirichativapee
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Abstract

Background Pleomorphic liposarcoma (PLPS) accounts for less than 5% of liposarcoma, and its metastasis to bone is rare. As a high-grade tumor, PLPS is reported to be more invasive with high local recurrence and distant metastasis. Here, we report a case of PLPS of the femur and undertake a review of the literature. Case Presentation. A 58-year-old man presented with a big mass at posterior aspect of his left thigh. The computed tomography of the chest for staging revealed two nodules at the left upper lung field. Wide resection of the soft tissue mass at the left thigh was performed by a general surgeon. Thoracotomy and wedge resection of the lung nodules was carried out by a cardiothoracic surgeon. Pathologic diagnosis suggested PLPS. Three years later, he was presented with sudden right hip pain after he slipped. The plain radiograph revealed an osteolytic lesion at the right proximal femur with minimally displaced pathological fracture. The MRI showed the presence of a tumor at the proximal part of the right femur and its soft tissue invasion. The patient underwent en bloc proximal femur wide resection followed by cemented long-stem bipolar hemiarthroplasty. The final histopathology report from definite surgery specimen revealed pleomorphic spindle, round, and polygonal cells arranged in sheets, short fascicles, and storiform arrays. There were no complications, adverse outcomes, or recurrence reported at six months after surgery. The patient could walk without gait aid and had good functional outcomes according to the TESS questionnaire. Conclusion PLPS is a highly aggressive tumor with a high distant metastatic rate. The definite diagnosis of PLPS is made on the basis of histopathology. Surgical treatment involving wide resection that aims to achieve a negative margin is the best option currently available, and we recommend treating bone metastasis from PLPS as the primary site of the tumor. The effect of chemotherapy and radiotherapy in preventing postoperative recurrence is still unclear and requires further studies.
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股骨多形性脂肪肉瘤:一种罕见的骨转移软组织肉瘤病例报告及文献复习
背景:多形性脂肪肉瘤(PLPS)在脂肪肉瘤中所占的比例不到5%,其骨转移性较少见。作为一种高级别肿瘤,PLPS具有侵袭性,具有高局部复发和远处转移。在此,我们报告一例股骨PLPS,并对相关文献进行回顾。案例演示。男性,58岁,左大腿后部有一大块肿块。胸部计算机断层扫描分期显示两个结节在左上肺野。由普通外科医生广泛切除左大腿软组织肿块。由心胸外科医生施行开胸楔形肺结节切除术。病理诊断提示PLPS。三年后,他在滑倒后突然出现右髋关节疼痛。x线平片显示右侧股骨近端溶骨性病变伴轻度移位病理性骨折。MRI显示右侧股骨近端肿瘤及软组织浸润。患者接受整块股骨近端全切除术,随后行骨水泥长柄双极半关节置换术。手术标本的最终组织病理学报告显示多形性梭形、圆形和多边形细胞呈片状排列、短束状排列和故事状排列。术后6个月无并发症、不良结果或复发报告。根据TESS问卷,患者无需步态辅助即可行走,功能预后良好。结论PLPS是一种侵袭性强、远处转移率高的肿瘤。PLPS的明确诊断是基于组织病理学。手术治疗包括广泛切除,目的是达到负切缘是目前可用的最佳选择,我们建议将PLPS骨转移作为肿瘤的原发部位进行治疗。化疗和放疗对预防术后复发的作用尚不清楚,需要进一步研究。
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审稿时长
14 weeks
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