Sati Alok, Ramappa Muralidhar, Chaurasia Sunita, Prasad Sitarama M
Department of Cornea and Anterior Segment Services, L V Prasad Eye Institute, Hyderabad, Andhra Pradesh, India.
BMJ Case Rep. 2014 Apr 4;2014:bcr2013202730. doi: 10.1136/bcr-2013-202730.
A 12-year-old boy with Hurler-Scheie syndrome (H/S syndrome) reported with reduced vision in both the eyes for past few years. Deep anterior lamellar keratoplasty (DALK) was performed for visual rehabilitation in his left eye. During surgery, the predescemet's plane was reached by meticulously dissecting the lamellar fibres using a manual technique. Histopathology of the dissected cornea showed the presence of numerous alcian blue positive deposits corroborating with the diagnosis of mucopolysaccharidosis (MPS). Postoperative course was uneventful. One year following surgery, the graft was clear and had a visual acuity of 20/50 with +1.00 170° - 0.75 refractive correction. Endothelial cell count, as measured by non-contact specular microscopy, was 2473.4 cells/mm(2). This case report highlights the application of DALK in a case of MPS-related corneal stromal opacification.
一名患有Hurler-Scheie综合征(H/S综合征)的12岁男孩,在过去几年中双眼视力下降。为其左眼进行了深板层角膜移植术(DALK)以恢复视力。手术过程中,通过手动技术仔细分离板层纤维到达了后弹力层平面。所分离角膜的组织病理学检查显示存在大量阿尔辛蓝阳性沉积物,证实了黏多糖贮积症(MPS)的诊断。术后过程平稳。术后一年,移植片透明,视力为20/50,屈光矫正为+1.00 170° - 0.75。通过非接触式角膜内皮显微镜测量,内皮细胞计数为2473.4个细胞/mm²。本病例报告强调了DALK在MPS相关角膜基质混浊病例中的应用。