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与眼眶黑变病相关的原发性眼眶黑色素瘤。

Primary orbital melanoma associated with orbital melanocytosis.

作者信息

Rice C D, Brown H H

机构信息

Department of Ophthalmology, University of Arkansas for Medical Sciences, Little Rock 72205.

出版信息

Arch Ophthalmol. 1990 Aug;108(8):1130-4. doi: 10.1001/archopht.1990.01070100086040.

Abstract

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.

摘要

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。

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