Alveolar Soft Part Sarcoma of the Extremity: Case Report and Literature Review

Khaled J. Ata, Hani N. Farsakh, Anwar Rjoop, Ismail Matalka, Liqa A. Rousan

Abstract


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.




World J Oncol. 2014;5(1):47-51
doi: http://dx.doi.org/10.14740/wjon777w

Keywords


Alveolar soft part sarcoma; Extremity sarcoma

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