Zhang Kai, Wang Yuanyuan, Li Yi
Department of Oncology, 920th Hospital of Joint Logistics Support Force, Kunming, China.
Department of Pathology, 920th Hospital of Joint Logistics Support Force, Kunming, China.
Respir Med Case Rep. 2025 Jul 25;57:102270. doi: 10.1016/j.rmcr.2025.102270. eCollection 2025.
Primary pulmonary synovial sarcoma (PPSS) is an extremely rare intrathoracic soft tissue sarcoma, but there remains a notable absence of consensus guidelines for the diagnosis and treatment of these tumors. In this case, we reported a 35-year-old PPSS patient who received neoadjuvant chemotherapy consisting of adriamycin and ifosfamide combined with anlotinib, a multi-target tyrosine kinase inhibitor. Although initial response assessment was not encouraging, subsequent imaging studies revealed therapeutic efficacy. This case underscores the critical role of multidisciplinary team and neoadjuvant therapy in PPSS management, aiming to raise awareness of this rare malignancy.
原发性肺滑膜肉瘤(PPSS)是一种极其罕见的胸内软组织肉瘤,但目前对于这些肿瘤的诊断和治疗仍缺乏显著的共识指南。在本病例中,我们报告了一名35岁的PPSS患者,其接受了由阿霉素和异环磷酰胺联合多靶点酪氨酸激酶抑制剂安罗替尼组成的新辅助化疗。尽管初始反应评估并不乐观,但随后的影像学研究显示了治疗效果。该病例强调了多学科团队和新辅助治疗在PPSS管理中的关键作用,旨在提高对这种罕见恶性肿瘤的认识。