Pasternak S, O'Connell J X, Verchere C, Rootman J
Department of Ophthalmology, Vancouver Hospital and Health Sciences Centre, BC, Canada.
Am J Ophthalmol. 1996 Sep;122(3):444-5. doi: 10.1016/s0002-9394(14)72081-1.
To report a documented case of orbital enchondroma.
A 25-year-old woman had an asymptomatic orbital mass. Computed tomographic scan was performed. The mass was surgically removed from the medial wall of the orbit, and the specimen was submitted for histopathologic examination.
The tumor showed typical radiologic and histopathologic appearance of an enchondroma with typical hypocellular lobules of cartilage enclosed by lamellar bone.
Cartilaginous neoplasms in the orbit are extremely rare.
报告一例有文献记载的眼眶内生软骨瘤病例。
一名25岁女性有一个无症状的眼眶肿物。进行了计算机断层扫描。该肿物从眼眶内侧壁手术切除,标本送组织病理学检查。
肿瘤表现出内生软骨瘤典型的放射学和组织病理学特征,有由板层骨包绕的典型软骨细胞稀少小叶。
眼眶软骨性肿瘤极为罕见。