Gaonker C H, Mukherjee A K, Pokle M
Department of Ophthalmology, Goa Medical College, Panaji.
Indian J Ophthalmol. 1992 Jan-Mar;40(1):2-4.
11 individuals were diagnosed to have neurofibromatosis type 1 and were examined for evidence of any ophthalmic lesions. Lisch nodules were the commonest manifestation of the disease and were present in 73% of all the patients (88% of those aged 16 years or more). 55% of the cases showed presence of neurofibroma on the lids. Other findings were optic glioma, unilateral sphenoid dysplasia with enlarged orbit, medullated nerve fibers and prominent corneal nerves with an incidence of 9% each.
11名个体被诊断患有1型神经纤维瘤病，并接受了眼部病变证据的检查。Lisch结节是该疾病最常见的表现，在所有患者中占73%（16岁及以上患者中占88%）。55%的病例显示眼睑存在神经纤维瘤。其他发现包括视神经胶质瘤、单侧蝶骨发育异常伴眼眶增大、有髓神经纤维和角膜神经增粗，每种情况的发生率均为9%。
