Bullen C L, Liesegang T J, McDonald T J, DeRemee R A
Ophthalmology. 1983 Mar;90(3):279-90. doi: 10.1016/s0161-6420(83)34574-7.
140 patients with biopsy-proven Wegener's granulomatosis were examined during a 16-year period at the Mayo Clinic. Forty patients had diverse and explosive ophthalmic involvement, including conjunctivitis, episcleritis, scleritis, corneal ulceration, uveitis, retinal vasculitis, optic neuropathy, orbital mass, orbital cellulitis, and obstruction of the nasolacrimal duct. The multiple ophthalmic and systemic complications in these 40 patients and the importance of establishing the pathologic diagnosis are discussed. Treatment with corticosteroids and immunosuppressive agents has dramatically improved the prognosis, although substantial mortality (four patients died of Wegener's granulomatosis) and ocular morbidity (three eyes were enucleated) are still associated with this disease.
在梅奥诊所的16年期间,对140例经活检证实为韦格纳肉芽肿病的患者进行了检查。40例患者有多样且严重的眼部受累情况,包括结膜炎、巩膜外层炎、巩膜炎、角膜溃疡、葡萄膜炎、视网膜血管炎、视神经病变、眼眶肿物、眼眶蜂窝织炎以及鼻泪管阻塞。讨论了这40例患者的多种眼部和全身并发症以及确立病理诊断的重要性。尽管仍有相当的死亡率(4例患者死于韦格纳肉芽肿病)和眼部发病率(3只眼被摘除)与该病相关,但使用皮质类固醇和免疫抑制剂治疗已显著改善了预后。