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ASPS tends to settle most frequently on the trunk and extremities, but previous studies reported its locations in other body sites. Similar to some other soft tissue sarcomas, the tumor grows slowly and also progresses painlessly. Such cases are often not detected early, and unfortunately, patients are metastatic at the time of diagnosis [1,4]. In the majority of soft tissue sarcomas, the primary treatment is surgical resection. This treatment also applies to ASPS. Adjuvant radiotherapy and chemotherapy are options that can be used to provide local control in the presence of metastasis [2, 5]. This study aimed to define the epidemiology and survival rates of ASPS with information obtained from the Surveillance, Epidemiology, and End Results (SEER) database.

Alveolar soft-part sarcoma: Analysis of 312 cases