Zhu Zejin, Rife Lawrence, Yiu Samuel, Trousdale Melvin D, Wasilewski Daniel, Siqueira Alexandre, Smith Ronald E
Doheny Eye Institute, Los Angeles, CA 90033, USA.
Cornea. 2006 Jul;25(6):705-8. doi: 10.1097/01.ico.0000214229.21238.eb.
Replacing diseased corneal endothelium with a preparation of Descemet membrane carrying functional endothelium and no stroma may be a feasible method for treating corneal endothelial decompensation. To obtain a viable donor of a Descemet membrane endothelium disc, we modified the Descemet membrane stripping technique and monitored the percentage of endothelial damage to the donor tissue preparation.
Forty-eight human corneas were used. Cornea buttons were mounted on an artificial anterior chamber, endothelial side up. Endothelia were stained with alizarin red, examined under the microscope, and photographed at 5 different sites (microscope, x100; digital magnification, x2.83). A 6 x 7-mm rectangular piece of endothelium-Descemet membrane complex was obtained using a Grieshaber microsurgical knife and Kelman-McPherson forceps. Digital photographs of endothelia were analyzed with a computer, and the percentage of endothelial damage was calculated. Specimens were processed for hematoxylin-eosin staining.
Forty of 48 endothelium-Descemet membrane preparations (83.3%) were complete peels with minimal endothelial damage. Endothelial damage before and after the surgery was 1.57 +/- 2.11% and 2.61 +/- 1.77%, respectively. Eight preparations (16.7%) failed because of tearing. Multiple hematoxylin-eosin-stained sections showed the presence of endothelium with intact Descemet membrane and no stromal tissue.
We modified the technique of Melles and obtained a sheet of Descemet membrane and endothelium with minimal endothelial damage and with no remaining stroma observed. This simple technique can be used to obtain the endothelium-Descemet membrane complex in minutes. It may be useful for corneal endothelium transplantation.
用携带功能性内皮细胞且无基质的Descemet膜制剂替代病变的角膜内皮,可能是治疗角膜内皮失代偿的一种可行方法。为了获得可行的Descemet膜内皮盘供体,我们改进了Descemet膜剥离技术,并监测供体组织制剂中内皮损伤的百分比。
使用48个人类角膜。将角膜纽扣内皮面朝上安装在人工前房上。用茜素红对内皮细胞进行染色,在显微镜下检查,并在5个不同部位拍照(显微镜,×100;数字放大,×2.83)。使用Grieshaber显微手术刀和Kelman-McPherson镊子获取一块6×7毫米的内皮-Descemet膜复合体矩形片。用计算机分析内皮细胞的数码照片,并计算内皮损伤的百分比。对标本进行苏木精-伊红染色处理。
48个内皮-Descemet膜制剂中有40个(83.3%)为完整剥离,内皮损伤最小。手术前后的内皮损伤分别为1.57±2.11%和2.61±1.77%。8个制剂(16.7%)因撕裂而失败。多个苏木精-伊红染色切片显示存在内皮细胞,Descemet膜完整且无基质组织。
我们改进了Melles的技术,获得了一片Descemet膜和内皮,内皮损伤最小且未观察到残留基质。这种简单的技术可在数分钟内用于获取内皮-Descemet膜复合体。它可能对角膜内皮移植有用。