Miller K H, Green W R, Stark W J, Wells H A, Mendelsohn G, Kanhofer H
Ophthalmology. 1980 Sep;87(9):944-50. doi: 10.1016/s0161-6420(80)35154-3.
A 63-year old woman had bilateral, multi-level corneal deposits distributed as fine, discrete crystals and in dense, deep geographic patches. She had a long history of sero-positive rheumatoid arthritis. Autopsy revealed an unsuspected lymphoproliferative disorder and immune-complex disease. Histologic examination of the eyes revealed eosinophilic, PAS-positive, noncollagenous deposits in the cornea at all levels and also in the ciliary processes, pars plana, and choroid. Stains for gold, amyloid, and acid mucopolysaccharides were negative. Immunoperoxidase stains were positive for IgG most strongly, and also for IgA, kappa and lambda light chains. Transmission electron microscopy showed needle-like electron-dense extracellular particles which we presume are immunoglobulins.
一名63岁女性双眼出现多层角膜沉积物,呈细小、离散的晶体状以及密集、深层的地图状斑块分布。她有血清阳性类风湿性关节炎的长期病史。尸检发现一种未被怀疑的淋巴增殖性疾病和免疫复合物疾病。眼部组织学检查显示,角膜各层以及睫状体、睫状平坦部和脉络膜均有嗜酸性、PAS阳性、非胶原性沉积物。金、淀粉样蛋白和酸性粘多糖染色均为阴性。免疫过氧化物酶染色显示IgG阳性最强,IgA、κ和λ轻链也呈阳性。透射电子显微镜显示针状电子致密细胞外颗粒,我们推测其为免疫球蛋白。