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眼眶沙砾样(青少年型)骨化性纤维瘤

Psammomatoid (juvenile) ossifying fibroma of the orbit.

作者信息

Margo C E, Ragsdale B D, Perman K I, Zimmerman L E, Sweet D E

出版信息

Ophthalmology. 1985 Jan;92(1):150-9. doi: 10.1016/s0161-6420(85)34070-8.

Abstract

The clinical and pathologic features in 21 cases of a distinctive solitary fibro-osseous lesion affecting the orbit distinguished histologically by the dominance of numerous small round "psammoma-like" ossicles embedded in a cellular benign spindle cell stroma were studied. The patients were predominantly young, and 19 of the lesions were centered on the orbital plate of the frontal bone or ethmoid. A clinical course of slowly progressive symptoms over several years was typical but not uniform. The most common clinical diagnosis was fibrous dysplasia and mucocele. At least nine patients underwent two or more surgical operations; one patient had six recurrences over a 15-year period. There were no known deaths from the tumor, but its potentially massive size can result in considerable morbidity and cosmetic deformity. Although previously referred to as active juvenile ossifying fibroma, the term psammomatoid ossifying fibroma for this lesion is more descriptive and has historical precedence.

摘要

对21例累及眼眶的一种独特的孤立性纤维-骨病变进行了研究,该病变在组织学上的特征是在细胞性良性梭形细胞基质中存在大量小圆形“砂粒体样”小骨片占优势。患者以年轻人为主,19个病变集中在额骨或筛骨的眶板。典型的临床病程是数年缓慢进展的症状,但并不一致。最常见的临床诊断是骨纤维异常增殖症和黏液囊肿。至少9例患者接受了两次或更多次手术;1例患者在15年期间复发6次。尚无该肿瘤导致死亡的报道,但它潜在的巨大体积可导致相当大的发病率和美容畸形。尽管该病变以前被称为活跃性幼年骨化性纤维瘤,但砂粒体样骨化性纤维瘤这一术语对该病变更具描述性且有历史先例。

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