Ichiki Yoshinobu, Kakizoe Keisei, Hamatsu Takayuki, Matsuyama Atsuji, Suehiro Taketoshi, Tanaka Fumihiro, Hisaoka Masanori, Sugimachi Keizo
Department of Chest Surgery, Onga Nakama Medical Association Onga Hospital, 1725-2 Ooaza-Ozaki Ongacho, Onga-gun, Fukuoka, 811-4342, Japan.
Department of Surgery, Onga Nakama Medical Association Onga Hospital, Onga-gun, Fukuoka, Japan.
Surg Case Rep. 2017 Dec;3(1):10. doi: 10.1186/s40792-016-0286-7. Epub 2017 Jan 7.
Solitary fibrous tumors (SFTs) are relatively rare neoplasms that commonly occur in the pleura. The pathological feature of SFTs is a proliferation of spindle-shaped cells in interlacing or storiform fascicles. SFTs appear to derived from pluripotential submesothelial cells, but not the covering mesothelium. SFTs distinctively show diffuse staining for CD34 but lack staining for smooth muscle markers. We herein report a relatively rare case of a 68-year-old male patient without symptoms, who underwent resection for what was considered to be SFT.
孤立性纤维性肿瘤(SFTs)是相对罕见的肿瘤,通常发生于胸膜。SFTs的病理特征是梭形细胞在交错或束状排列的纤维组织中增生。SFTs似乎起源于多能间皮细胞,而非覆盖的间皮。SFTs显著表现为CD34弥漫性染色,但平滑肌标志物染色阴性。我们在此报告一例相对罕见的病例,一名68岁无症状男性患者,因被认为是SFT而接受了切除术。