Haritoglou C, Ugele B, Kenyon K R, Kampik A
Department of Ophthalmology, Ludwig-Maximilians University, Munich, Germany.
Cornea. 2000 Nov;19(6):861-3. doi: 10.1097/00003226-200011000-00023.
To report the unusual manifestation of X-linked ichthyosis in two brothers.
Leukocyte separation and sterylsulfatase assay are performed to show the deficiency of sterylsulfatase.
Two brothers presented in our clinic with cutaneous alterations consistent with X-linked ichthyosis. Ocular examination disclosed fine, flour-like, punctate, evenly, and diffusely distributed opacities of the posterior corneal stroma, close to Descemet membrane in both patients. In one patient, superficial, small, granular opacities were detected. They were gray in color and seemed to involve the epithelium and the subepithelial and anterior stromal layers. In both patients, the deficiency of sterylsulfatase could be shown and confirmed the diagnosis.
Flour-like opacities in the posterior stroma have been shown to be a common manifestation of X-linked ichthyosis. Though the underlying biochemical defect in X-linked ichthyosis has been discovered, the question of how these opacities develop is still a subject of debate. Subepithelial stromal keratopathies or epithelial irregularities are uncommon and are rarely described in the literature. The superficial corneal changes seen in one of our patients are unusual and are not similar to those reported by other authors.
报告两兄弟患X连锁鱼鳞病的不寻常表现。
进行白细胞分离和类固醇硫酸酯酶检测以显示类固醇硫酸酯酶缺乏。
两兄弟在我们诊所就诊,皮肤改变符合X连锁鱼鳞病。眼科检查发现两名患者后角膜基质均有细小、面粉样、点状、均匀且弥漫分布的混浊,靠近Descemet膜。在一名患者中,检测到浅表、小的颗粒状混浊。它们呈灰色,似乎累及上皮、上皮下和前基质层。在两名患者中,均可显示类固醇硫酸酯酶缺乏,从而确诊。
后基质中的面粉样混浊已被证明是X连锁鱼鳞病的常见表现。尽管X连锁鱼鳞病的潜在生化缺陷已被发现,但这些混浊如何形成的问题仍存在争议。上皮下基质角膜病变或上皮不规则并不常见,文献中很少描述。我们其中一名患者所见的浅表角膜改变不寻常,与其他作者报道的不同。