Asokan B, Ramanan P, Sundararaj M, Kovarthini E
Department of Plastic Surgery, Coimbatore Medical College, Coimbatore, Tamil Nadu, India.
Indian J Plast Surg. 2017 Sep-Dec;50(3):310-313. doi: 10.4103/ijps.IJPS_14_15.
Alveolar soft part sarcoma (ASPS) is a rare form of soft-tissue sarcoma arising from connective tissue. It is most often seen in adolescents and young adults and has high propensity for recurrence and metastasis. Clinically, it mimics haemangioma or arteriovenous malformations. In our case report, an 18-year-old female presented with markedly vascular tumour in the left forearm, for which excision biopsy was done. Histopathological report revealed ASPS. The patient was screened for metastasis. Ultrasound abdomen, computed tomography (CT) chest, CT brain and whole-body skeletal survey was done. The patient was found to have bilateral pulmonary metastasis. The patient was given 6 cycles of chemotherapy with adriamycin, cyclophosphamide and vincristine. There was no locoregional and pulmonary recurrence for 11 months after being treated by excision of the tumour followed by chemotherapy.
肺泡软组织肉瘤(ASPS)是一种罕见的起源于结缔组织的软组织肉瘤。它最常见于青少年和年轻人,具有很高的复发和转移倾向。临床上,它类似于血管瘤或动静脉畸形。在我们的病例报告中,一名18岁女性左前臂出现明显的血管性肿瘤,为此进行了切除活检。组织病理学报告显示为ASPS。对该患者进行了转移筛查。进行了腹部超声、胸部计算机断层扫描(CT)、脑部CT和全身骨骼检查。发现该患者有双侧肺转移。该患者接受了6个周期的阿霉素、环磷酰胺和长春新碱化疗。在肿瘤切除后进行化疗,11个月内未出现局部和肺部复发。