| Literature DB >> 27588141 |
Xiaolong Yu1, Yong Yang2, Bin Zhang1, Hucheng Liu3, Runsheng Guo3, Min Dai1.
Abstract
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 cm3 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.Entities:
Keywords: immunohistochemistry; misdiagnosis; pathology; pleomorphic rhabdomyosarcoma; right thigh; surgery; young adult
Year: 2016 PMID: 27588141 PMCID: PMC4998024 DOI: 10.3892/ol.2016.4819
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967