Rice C D, Brown H H
Department of Ophthalmology, University of Arkansas for Medical Sciences, Little Rock 72205.
Arch Ophthalmol. 1990 Aug;108(8):1130-4. doi: 10.1001/archopht.1990.01070100086040.
We report a case of primary orbital melanoma in a 17-year-old girl. The patient presented with painless proptosis during the first trimester of pregnancy. Computed tomography demonstrated a well-circumscribed mass located infra-temporally in the right orbit. The tumor was bluish-black, grossly encapsulated, and associated with orbital blue nevi. Histologic examination of the mass revealed a pigmented spindle-cell neoplasm. On electron microscopy, the presence of premelanosomes and the absence of basal lamina supported the diagnosis of melanoma. Malignant transformation of a preexisting nevus is postulated since perineural foci of benign dendritic melanocytes were seen within the melanoma. There has been no recurrence or metastasis in a 2-year follow-up. Of 30 primary orbital melanomas reviewed, 12 (40%) were associated with periorbital pigmentary disorders, such as oculodermal melanocytosis, blue nevus, and ocular melanocytosis. Our case is unique since the pigmentary lesions were limited to the orbital tissues.
我们报告一例17岁女孩的原发性眼眶黑色素瘤。患者在妊娠早期出现无痛性眼球突出。计算机断层扫描显示右眼眶颞下有一个边界清晰的肿块。肿瘤呈蓝黑色,肉眼可见有包膜,且与眼眶蓝色痣有关。对肿块进行组织学检查发现是一种色素性梭形细胞瘤。电子显微镜检查显示有前黑素小体且无基底膜,支持黑色素瘤的诊断。由于在黑色素瘤内可见良性树枝状黑素细胞的神经周围病灶,推测为先前存在的痣发生了恶性转化。在2年的随访中未出现复发或转移。在回顾的30例原发性眼眶黑色素瘤中,12例(40%)与眶周色素沉着紊乱有关,如眼皮肤黑素细胞增多症、蓝色痣和眼部黑素细胞增多症。我们的病例很独特,因为色素沉着病变仅限于眼眶组织。