摘要
患者,50岁,女,患有无痛性Wegener肉芽肿病,侵犯肺部及鼻窦,双侧穿孔性巩膜软化,双侧周边角膜变薄(接触镜角膜)及单侧眼眶炎症。患者初次诊断为系统性疾病后存活12a,左眼球外伤后穿孔,直到最后一次复诊右眼球没有穿孔。
A rare case of bilateral scleromalacia perforans, bilateral peripheral corneal thinning （contact lens cornea） and unilateral orbital inflammatory disease in a 50 year old female patient with an indolent form Wegener＇s granulomatosis （WG） involving lungs and sinuses is reported. The patient survived for 12 years after the initial diagnosis of systemic disease. There was perforation of left globe following trauma and no perforation of the right globe till the last follow up of the patient.
出处
《国际眼科杂志》
CAS
2009年第7期1239-1242,共4页
International Eye Science
