Horie Y, Ikawa S, Okamoto I, Nagata M, Tamai A
Department of Clinical Laboratory Medicine, Faculty of Medicine, Tottori University, Japan.
Jpn J Ophthalmol. 1995;39(1):77-82.
A rare case of conjunctival myxoma is reported. A painless tumor was noted in the left bulbar conjunctiva of an 80-year-old woman. The extirpated tumor, 12 x 10 mm, was hypocellular and composed of spindle-shaped or stellate tumor cells. The tumor stroma showed extensive myxomatous changes. Alcian blue stain with hyaluronidase digestion revealed that the matrix contained rich amounts of hyaluronidase-sensitive acid mucopolysaccharides. Immunohistochemically, the tumor cells were positive for vimentin and alpha-smooth muscle actin, suggesting a fibroblastic or myofibroblastic cell phenotype. A review of the literature revealed the rare incidence and invariable benign behavior of conjunctival myxoma.
报告了一例罕见的结膜黏液瘤病例。一名80岁女性的左眼球结膜发现一个无痛性肿瘤。切除的肿瘤大小为12×10毫米,细胞稀少,由梭形或星状肿瘤细胞组成。肿瘤基质显示广泛的黏液瘤样改变。阿利新蓝染色加透明质酸酶消化显示基质中含有大量对透明质酸酶敏感的酸性黏多糖。免疫组织化学检查显示,肿瘤细胞波形蛋白和α-平滑肌肌动蛋白呈阳性,提示为成纤维细胞或肌成纤维细胞表型。文献回顾显示结膜黏液瘤发病率低且行为始终为良性。