Nik N A, Martin N F, Berler D K
Ann Ophthalmol. 1985 May;17(5):303-7, 310.
An unusual case is presented in which corneal deposits in mid-to-deep stroma with Doyne's posterior pole drusenosis are the initial signs of an IgA-kappa monoclonal gammopathy. The case has several unique features. Corneal deposits have been described previously with IgG and IgM-kappa light chain gammopathies, but to our knowledge have not been described before with IgA-kappa monoclonal gammopathy. Corneal stromal deposits and associated macular drusen have been described with IgM monoclonal gammopathy, but not previously with IgA monoclonal gammopathy. Bietti described superficial perilimbal corneal deposits with fundus albipunctatus, whereas the present case shows diffuse central deep corneal deposits with macular drusen.
本文报告了一例罕见病例,其中中至深层基质的角膜沉积物伴多伊内后极玻璃膜疣病是IgA-κ单克隆丙种球蛋白病的初始体征。该病例有几个独特特征。先前已描述过角膜沉积物与IgG和IgM-κ轻链丙种球蛋白病相关,但据我们所知,此前尚未有与IgA-κ单克隆丙种球蛋白病相关的描述。角膜基质沉积物及相关黄斑玻璃膜疣已在IgM单克隆丙种球蛋白病中有所描述,但此前未见于IgA单克隆丙种球蛋白病。别蒂曾描述过伴有白点状眼底的浅层角膜缘沉积物,而本病例显示的是伴有黄斑玻璃膜疣的弥漫性中央深层角膜沉积物。