Mamalis N, Grey A M, Good J S, McLeish W M, Anderson R L
Intermountain Ocular Research Center, Department of Ophthalmology, University of Utah, Salt Lake City.
Ophthalmic Surg. 1994 May;25(5):332-5.
A 35-year-old man had rapidly progressive proptosis of the right eye with associated chemosis over a period of several weeks. Computed tomography demonstrated a solid extraconal mass in the inferior anterior right orbit. Pathologic examination revealed the lesion to be an embryonal rhabdomyosarcoma. Consistent with the diagnosis, immunohistochemical assays demonstrated positive staining with myoglobin, desmin, and muscle-specific actin. The lesion grew rapidly and was further surgically excised. Subsequently, treatment with radiation and chemotherapy was initiated. Primary embryonal rhabdomyosarcoma of the orbit is an extremely rare tumor in adults, and, to our knowledge, this patient represents the oldest individual reported to have developed such a tumor, as documented by immunohistochemical analysis.
一名35岁男性在数周内右眼迅速出现进行性眼球突出并伴有球结膜水肿。计算机断层扫描显示右眼眶前下部有一个实性眶外肿块。病理检查显示该病变为胚胎性横纹肌肉瘤。与诊断一致,免疫组织化学检测显示肌红蛋白、结蛋白和肌肉特异性肌动蛋白呈阳性染色。病变迅速生长,进一步进行了手术切除。随后,开始进行放疗和化疗。眼眶原发性胚胎性横纹肌肉瘤在成人中极为罕见,据我们所知,经免疫组织化学分析证实,该患者是报告中患此病年龄最大的个体。