Yu Xiaolong, Yang Yong, Zhang Bin, Liu Hucheng, Guo Runsheng, Dai Min
Department of Orthopedics, The First Affiliated Hospital of Nanchang University, Artificial Joints Engineering and Technology Research Center of Jiangxi Province, Nanchang, Jiangxi 330006, P.R. China.
Department of Orthopedics, Xinyu People's Hospital, Xinyu, Jiangxi 338025, P.R. China.
Oncol Lett. 2016 Sep;12(3):1921-1924. doi: 10.3892/ol.2016.4819. Epub 2016 Jul 7.
Pleomorphic rhabdomyosarcoma (PRMS) is a rare type of soft tissue tumor accounting for <2% of all adult sarcomas. The present study describes a case of a 28-year-old male patient with primary PRMS of the right thigh. The patient was initially diagnosed with a schwannoma and underwent conservative therapy at a local hospital. At the 6-month follow-up, the patient reported a marked increase in the size of the mass. Finally, the patient underwent fine-needle aspiration and total tumor resection. The tumor measured 11×9×5 cm in size and was located in the vastus intermedius muscle. According to histological and immunohistochemical findings, a diagnosis of PRMS was confirmed by an expert pathology consultant. Postoperative follow-up at 3 months revealed no evidence of recurrent disease or residual side effects from therapy. However, it is imperative that such cases are closely monitored following surgery, in order to evaluate the long-term efficacy of the procedure, since misdiagnosis may increase the risk of recurrence and metastasis. The present case is noteworthy due to the misdiagnosis of PRMS, the large size of the mass and the young age of the patient.
多形性横纹肌肉瘤(PRMS)是一种罕见的软组织肿瘤,占所有成人肉瘤的比例不到2%。本研究描述了一例28岁男性患者,患有右大腿原发性PRMS。该患者最初被诊断为神经鞘瘤,并在当地医院接受了保守治疗。在6个月的随访中,患者报告肿块大小显著增加。最后,患者接受了细针穿刺和肿瘤全切术。肿瘤大小为11×9×5 cm,位于股中间肌。根据组织学和免疫组化结果,一名专业病理顾问确诊为PRMS。术后3个月的随访显示,没有疾病复发或治疗残留副作用的证据。然而,由于误诊可能会增加复发和转移的风险,因此术后必须密切监测此类病例,以评估手术的长期疗效。由于PRMS的误诊、肿块较大以及患者年龄较轻,本病例值得关注。