VanDenBerg Ryan, Diakonis Vasilios F, Bozung Alison, Gameiro Gustavo Rosa, Fischer Oliver, El Dakkak Ahmed, Ulloa-Padilla Jan Paul, Anagnostopoulos Apostolos, Dubovy Sander, Abou Shousha Mohamed
Bascom Palmer Eye Institute, University of Miami, Miami, FL.
Cornea. 2017 Dec;36(12):1535-1537. doi: 10.1097/ICO.0000000000001378.
To disclose, using an ex vivo study, the histopathological mechanism behind in vivo thickening of the endothelium/Descemet membrane complex (En/DM) observed in rejected corneal grafts (RCGs).
Descemet membrane (DM), endothelium, and retrocorneal membranes make up the total En/DM thickness. These layers are not differentiable by high-definition optical coherence tomography; therefore, the source of thickening is unclear from an in vivo perspective. A retrospective ex vivo study (from September 2015 to December 2015) was conducted to measure the thicknesses of DM, endothelium, and retrocorneal membrane in 54 corneal specimens (31 RCGs and 23 controls) using light microscopy. Controls were globes with posterior melanoma without corneal involvement.
There were 54 corneas examined ex vivo with mean age 58.1 ± 12.2 in controls and 51.7 ± 27.9 years in RCGs. The ex vivo study uncovered the histopathological mechanism of En/DM thickening to be secondary to significant thickening (P < 0.001) of DM (6.5 ± 2.4 μm) in RCGs compared with controls (3.9 ± 1.5 μm).
Our ex vivo study shows that DM is responsible for thickening of the En/DM in RCGs observed in vivo by high-definition optical coherence tomography and not the endothelium or retrocorneal membrane.
通过一项体外研究,揭示在排斥角膜移植片(RCG)中观察到的体内内皮/后弹力层复合体(En/DM)增厚背后的组织病理学机制。
后弹力层(DM)、内皮和角膜后膜构成了En/DM的总厚度。这些层在高分辨率光学相干断层扫描中无法区分;因此,从体内角度来看,增厚的来源尚不清楚。进行了一项回顾性体外研究(2015年9月至2015年12月),使用光学显微镜测量54个角膜标本(31个RCG和23个对照)中DM、内皮和角膜后膜的厚度。对照为患有后葡萄膜黑色素瘤但未累及角膜的眼球。
对54个角膜进行了体外检查,对照组的平均年龄为58.1±12.2岁,RCG组为51.7±27.9岁。体外研究发现,与对照组(3.9±1.5μm)相比,RCG组中En/DM增厚的组织病理学机制是由于DM显著增厚(P<0.001)(6.5±2.4μm)。
我们的体外研究表明,通过高分辨率光学相干断层扫描在体内观察到的RCG中En/DM增厚是由DM引起的,而非内皮或角膜后膜。