Rodríguez-Ares T, Varela-Durán J, Sánchez-Salorio M, Varela-Nuñez R, Capeans-Tomé C, Urdiales-Viedma M
Department of Ophthalmology and Pathology, University of Santiago Medical School and Hospital, Santiago de Compostela, Spain.
Eur J Ophthalmol. 1993 Jan-Mar;3(1):47-52. doi: 10.1177/112067219300300109.
The clinical and pathological characteristics of a myoblastoma of the orbital are described. The tumor presented as a painless hard mass in the left orbit of a 56-year-old caucasian male, causing diplopia and hypertrophy of the left eye in the primary visual position. Light microscopy studies revealed a typical granular cell tumor with PAS-positive intracytoplasmic granules. Immunoperoxidase studies showed positivity for S-100 protein and desmin. Electron microscopy studies showed numerous intracellular myelin degenerative bodies. The patient developed an epidermoid cyst at the site of initial surgery, but has no signs of local or distant disease two years after initial treatment.
本文描述了眼眶成肌细胞瘤的临床和病理特征。该肿瘤表现为一名56岁白种男性左眼眶内无痛性硬块,导致患者在第一眼位出现复视和左眼肥大。光学显微镜研究显示为典型的颗粒细胞瘤,胞浆内颗粒PAS染色呈阳性。免疫过氧化物酶研究显示S-100蛋白和结蛋白呈阳性。电子显微镜研究显示有大量细胞内髓鞘样变性小体。患者在初次手术部位出现了表皮样囊肿,但初次治疗两年后无局部或远处疾病迹象。