Satomi Takafumi, Hasegawa On, Abukawa Harutsugu, Kohno Michihide, Enomoto Ai, Chikazu Daichi, Matsubayashi Jun, Nagao Toshitaka
Department of Oral and Maxillofacial Surgery, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan,
Med Mol Morphol. 2014 Jun;47(2):108-16. doi: 10.1007/s00795-013-0054-8. Epub 2013 Sep 13.
Solitary fibrous tumor (SFT) is a rare mass-forming soft tissue tumor that occurs most commonly in the pleura, but has been described in various extrathoracic sites. Extrapleural manifestation of SFT, particularly in the head and neck region, is rare. The most common extrapleural site is the oral cavity; these tumors have also been described in the orbit, nasopharynx, paranasal sinuses, salivary glands, and larynx. We report an extremely rare case of a SFT in the subcutaneous region of the cheek. This tumor in the left cheek was a large firm mass, approximately 8.5 cm × 6 cm in size and was successfully treated by surgical resection. Immunohistochemistry revealed reactivity for vimentin, CD34, and bcl-2, but no staining for cytokeratin, epithelial membrane antigen, S-100, desmin, caldesmon, actin, α-smooth muscle actin, CD117, and CD99. Immunohistochemical study is the key to establish a definitive diagnosis of SFT, and ultrastructural study is also useful for making an accurate diagnosis. The patient recovered uneventfully without evidence of tumor recurrence 2 years after surgery.
孤立性纤维性肿瘤(SFT)是一种罕见的形成肿块的软组织肿瘤,最常见于胸膜,但也有在各种胸外部位的报道。SFT的胸膜外表现,尤其是在头颈部区域,很罕见。最常见的胸膜外部位是口腔;这些肿瘤也有在眼眶、鼻咽、鼻窦、唾液腺和喉部的报道。我们报告一例极其罕见的发生于脸颊皮下区域的SFT病例。左侧脸颊的这个肿瘤是一个大的坚实肿块,大小约为8.5厘米×6厘米,通过手术切除成功治愈。免疫组织化学显示波形蛋白、CD34和bcl-2呈阳性反应,但细胞角蛋白、上皮膜抗原、S-100、结蛋白、钙调蛋白、肌动蛋白、α-平滑肌肌动蛋白、CD117和CD99无染色。免疫组织化学研究是确立SFT明确诊断的关键,超微结构研究对准确诊断也有帮助。患者术后2年恢复良好,无肿瘤复发迹象。