Abstract. The present case report aimed to improve the understanding of alveolar soft part sarcoma (ASPS) by investigating the clinical characteristics, diagnosis and therapeutic methods used to treat ASPS associated with lung and brain metastases. The clinical data of a single patient diagnosed with ASPS by postoperative pathology was studied retrospectively, and additional associated reports and previous studies of similar cases were reviewed. Clinical symptoms were markedly alleviated following surgical treatment, followed by a chemotherapy regime. During post-treatment follow-up, no tumor recurrence was observed.
IntroductionAlveolar soft part sarcoma (ASPS) is a clinically rare soft tissue sarcoma (STS) of unknown histological origin, accounting for 0.5-1.0% of all STS cases, worldwide (1). ASPS associated with lung and brain metastases is a rare disease with poor prognosis, with a high risk of metastasis to the brain. Surgery is typically the primary method used in the treatment of ASPS (2). The present study outlines the case of a patient with ASPS and associated lung and brain metastases. The patient provided signed informed consent, and therefore the case is detailed in the following report, including the course of disease and patient outcome.
Case reportA 39-year-old male patient was admitted to the People's Hospital of Linyi City of Shandong Province (Linyi, China) on 3 January 2014, after experiencing occasional headaches during the previous 6 months. The patient's headaches had become progressively more severe 1 month prior to admission to hospital, and were associated with right upper limb weakness and inaccurate fine motor movements. Physical examination revealed negative cranial nerve-associated signs. Breath sounds were clear in both lungs, and no rhonchi or moist rales were heard. Distal right upper limb muscle strength received grade 4 (3), and tendon reflex and pathological signs were negative. As revealed by cranial computed tomography (CT; Fig. 1A), a high-density lesion was observed in the left postfrontal area [CT values, 52 Hounsfield units, (HU)] and a peripheral low-density edematous zone was visible. Magnetic resonance imaging (MRI) was also performed and revealed an irregular lump in the left frontal lobe with T1 and T2 hyperintensity. The surrounding vessels were belt-like and anfractuous with no intensified edematous regions (Fig. 1B-D). The medical history of the patient included resection of a subcutaneous mass in the left lower limb 10 years previously, which recurred 5 years later and required a second surgery. The masses resected during these earlier surgeries had not been sent for pathological examination. The patient reported no family history of the manifestations described above. Subsequently, the patient was further examined using chest radiography, which indicated multiple pulmonary nodules on both lungs. Therefore, the patient underwent single-photon emission CT/CT, which revealed no significant abnormalities on a whole-body bone scan (Fig. 1E). The chest CT result (Fig...