Hwang Sungsoon, Kim Yoon-Duck, Siapno Debrelle Lou, Suh Yeon-Lim, Woo Kyung In
Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Department of Ophthalmology, The Medical City, Pasig City, Metro Manilla, Philippines.
J Craniofac Surg. 2019 Jan;30(1):e19-e21. doi: 10.1097/SCS.0000000000004950.
Fibromyxomas are rare tumors that are not commonly seen in the orbit. The authors present a case of orbital fibromyxoma. A 42-year-old male presented with proptosis of the right eye that began 1 month prior. Magnetic resonance imaging revealed the presence of an orbital mass in the right eye, with low signal intensity on T1-weighted images and heterogeneous high-signal intensity on T2-weighted images. The patient underwent excisional biopsy of the orbital tumor through a Krönlein approach. The tumor originated from the inferior rectus muscle. Histopathologic analysis demonstrated scattered spindle cells, with both fibrous and myxoid stroma. Immunohistochemical staining was positive for Vimentin and negative for S-100 protein and CD34. The tumor was diagnosed as orbital fibromyxoma. The patient showed no evidence of recurrence over 18 months of follow-up after operation.
纤维黏液瘤是一种罕见肿瘤,在眼眶中并不常见。作者报告了一例眼眶纤维黏液瘤病例。一名42岁男性,1个月前开始出现右眼突出。磁共振成像显示右眼存在眼眶肿物,在T1加权图像上呈低信号强度,在T2加权图像上呈不均匀高信号强度。患者通过克伦莱因(Krönlein)入路接受了眼眶肿瘤切除活检。肿瘤起源于下直肌。组织病理学分析显示有散在的梭形细胞,伴有纤维性和黏液样基质。免疫组织化学染色波形蛋白(Vimentin)呈阳性,S-100蛋白和CD34呈阴性。该肿瘤被诊断为眼眶纤维黏液瘤。术后随访18个月,患者无复发迹象。