Cullen Eye Institute, Baylor College of Medicine, Department of Ophthalmology, Houston, TX 77030, USA.
Cornea. 2010 Jan;29(1):105-7. doi: 10.1097/ICO.0b013e31819e34ab.
The purpose of this study was to report an unusual pattern of immunoglobulin deposition in the corneas of a patient with dysproteinemia.
Clinical examination, slit lamp examination, a deep lamellar corneal biopsy, and serum and aqueous protein electrophoresis were obtained.
Slit lamp evaluation revealed amorphous, cloud-like opacities in the midperiphery at the level of deep stroma and Descemet's membrane. Electron microscopy demonstrated deep lamellar extracellular deposits consistent with immunoglobin. The serum protein electrophoresis revealed a monoclonal IgG kappa band, but the aqueous electrophoresis showed no bands in the gamma region.
This case documents a rare pattern of immunoglobulin deposition in the corneas in a patient with gammopathy. Despite its deep corneal distribution, the analysis of the aqueous specimen suggests that the source of the immunoglobulin is through a route other than from the aqueous.
本研究旨在报告一例伴有蛋白异常血症的患者角膜中免疫球蛋白沉积的一种不常见模式。
临床检查、裂隙灯检查、深层板层角膜活检以及血清和房水蛋白电泳。
裂隙灯检查显示在深层基质和Descemet 膜水平的中周边呈无定形云状混浊。电子显微镜显示深层板层细胞外沉积与免疫球蛋白一致。血清蛋白电泳显示单克隆 IgG κ 带,但房水电泳在 γ 区没有带。
本病例记录了一例伴有γ球蛋白病的患者角膜中罕见的免疫球蛋白沉积模式。尽管其在深层角膜分布,但对房水标本的分析表明免疫球蛋白的来源并非来自房水。