Ata Khaled J, Farsakh Hani N, Rjoop Anwar, Matalka Ismail, Rousan Liqa A
Department of Orthopedics, Jordan University of Science and Technology, King Abdullah University Hospital, Irbid, Jordan.
Department of Pathology, Jordan University of Science and Technology, King Abdullah University Hospital, Irbid, Jordan.
World J Oncol. 2014 Feb;5(1):47-51. doi: 10.14740/wjon777w. Epub 2014 Mar 11.
Alveolar soft part sarcoma (ASPS), a rare soft tissue sarcoma in children and adolescents, carries a poor prognosis. ASPS is an aggressive tumor of controversial histogenesis that, unlike other soft tissue sarcomas, tends to metastasize to the brain. A 9-year-old boy presented to our outpatient clinic in April 2009 with a chief complaint of a large painless mass in the left thigh whose size had increased significantly over the past 10 months. After staging the tumor, we performed open biopsy; the diagnosis was ASPS and he underwent wide local excision. In the course of 4-year follow-up by clinical and imaging studies, there was no evidence of early tumor recurrence or metastasis. Complete surgical resection is the treatment of choice in patients with ASPS.
肺泡软组织肉瘤(ASPS)是儿童和青少年中一种罕见的软组织肉瘤,预后较差。ASPS是一种组织发生存在争议的侵袭性肿瘤,与其他软组织肉瘤不同,它倾向于转移至脑部。一名9岁男孩于2009年4月到我们门诊就诊,主诉左大腿有一个无痛性大肿块,其大小在过去10个月中显著增大。对肿瘤进行分期后,我们进行了开放性活检;诊断为ASPS,随后他接受了广泛局部切除。在4年的临床和影像学随访过程中,没有早期肿瘤复发或转移的迹象。对于ASPS患者,完整的手术切除是首选治疗方法。