Yan Jianhua
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.
J Craniofac Surg. 2016 Oct;27(7):e607-e608. doi: 10.1097/SCS.0000000000002921.
PURPOSE/BACKGROUND: To report a rare patient with idiopathic orbital inflammatory pseudotumor showing obvious bone erosion of the orbital wall.
Clinical features and imaging findings, orbital surgery, and histopathological examination are presented.
A 56-year-old Chinese man showed a gradually growing unilateral proptosis of the left eye for 6 months. Visual acuity, intraocular pressure, anterior segment, and fundi were normal in both eyes. Proptosis was 17 mm in the right eye and 23 mm in the left. No palpable mass was present on the left orbital rim. Ocular motility showed a moderate limitation of left adduction. Computed tomography scan revealed multifocal smoothly outlined homogeneous soft tissue masses measuring from 10 × 6 to 30 × 10 mm with obvious bone destruction in the lateral and inferior walls of the left orbit. An anterior orbitotomy by an inferio-temporal skin incision was used to partially remove the mass. Histopathological evaluation confirmed the diagnosis of an idiopathic inflammatory pseudotumor. After surgery, administration of systemic corticosteroids was initiated, which resulted in a dramatic improvement in the proptosis and ocular movements. There was no recurrence as determined at 6 years postsurgery and visual acuity was 25/20 in both eyes.
Idiopathic orbital inflammatory pseudotumor may show an orbital bone erosion, similar to that of soft-tissue malignancy or orbital metastasis.
目的/背景:报告1例表现为眶壁明显骨质侵蚀的特发性眼眶炎性假瘤罕见病例。
介绍临床特征、影像学表现、眼眶手术及组织病理学检查情况。
1例56岁中国男性,左眼渐进性眼球突出6个月。双眼视力、眼压、眼前节及眼底均正常。右眼眼球突出度为17mm,左眼为23mm。左眼眶缘未触及肿块。眼球运动显示左眼内收中度受限。计算机断层扫描显示,左眼眶外侧壁和下壁有多个边界光滑的均匀软组织肿块,大小为10×6至30×10mm,伴有明显骨质破坏。采用颞下皮肤切口行前路眼眶切开术,部分切除肿块。组织病理学评估确诊为特发性炎性假瘤。术后开始全身应用糖皮质激素,眼球突出度和眼球运动明显改善。术后6年未见复发,双眼视力均为25/20。
特发性眼眶炎性假瘤可表现为眼眶骨质侵蚀,类似于软组织恶性肿瘤或眼眶转移瘤。