论文部分内容阅读
眼眶原发性脑膜瘤少见,占眼眶内肿瘤的0.77％,本文报告2例。此瘤生长缓慢,临床表现局部压迫症状,切除后很少复发,需要排除颅内脑膜瘤外延的可能。病例报告例1 女性,35岁,住院号98803。因左眼球突出、视物不清2年余,于1976年2月14日入院。当时,左眼球突出26mm,上睑肿胀无压痛,球结膜轻度充血、水肿,穹窿部血管怒张,眼球活动受限。眼底见乳头边界模糊,上方视网膜剥离。X线片示左眼眶、鼻窦及其骨壁均正常。于1976年2月16日左眼眶内容物剜除术,见肿物位于球后,与眼
Primary orbital meningioma rare, accounting for 0.77% of the orbital tumors, this report 2 cases. The slow growth of the tumor, clinical symptoms of local compression, rarely relapsed after resection, the need to rule out the possibility of intracranial meningioma. Case Report 1 Female, 35 years old, hospital number 98803. Due to the left eyeball prominent, depending on the material unclear more than 2 years, in February 14, 1976 admission. At that time, the left eye prominent 26mm, swelling of the upper eyelid no tenderness, bulbar conjunctiva mild congestion, edema, vault vasodilation, eye activity is limited. Fundus nipple see blurred vision, retinal detachment above. X-ray showed left orbit, sinus and bone wall were normal. On February 16, 1976 left orbital content removal surgery, see the tumor is located in the ball, with the eye