Mintz-Hittner H A, Kretzer F L
Cullen Eye Institute, Baylor College of Medicine, Houston, TX 77030.
Doc Ophthalmol. 1990 Mar;74(3):263-8. doi: 10.1007/BF02482617.
Our current surgical protocol for Zone I threshold retinopathy of prematurity (ROP) has evolved over 15 years and is rationalized by increasing knowledge of two pathologic processes of ROP: 1) angiogenic stimulation of spindle cells (clinically invisible) near the vitreal surface of the avascular retina; and 2) tractional forces of myofibroblasts [clinically visible as extraretinal fibrovascular proliferation (EFP)] in the vitreous overlying the vascular retina. These two pathologic processes occur concomitantly with normal anterior ocular growth with a constant optic disc-macular distance. Our current surgical protocol for Zone I threshold ROP, involves complex surgeries to achieve success defined as a macula which always remains anatomically attached, but which may be distorted or ectopic. This protocol requires cryotherapy in at least two sessions. The first is to the avascular retina to destroy spindle cells. The second is to the EFP to destroy myofibroblasts and to the shunt to eliminate the site of origin of myofibroblasts. The protocol also requires the concomitant placement of a prophylactic scleral buckle to allow formation of a new complete ora serrata while remnant myofibroblasts contract and while anterior ocular growth continues.
我们目前针对I区阈值性早产儿视网膜病变(ROP)的手术方案历经15年不断演变,并且基于对ROP两个病理过程的深入了解而变得更加合理:1)无血管视网膜玻璃体表面附近梭形细胞(临床不可见)的血管生成刺激;2)覆盖在血管化视网膜上方玻璃体中肌成纤维细胞的牵拉力(临床上表现为视网膜外纤维血管增殖,即EFP)。这两个病理过程与正常的眼前段生长同时发生,视盘-黄斑距离保持恒定。我们目前针对I区阈值性ROP的手术方案涉及复杂手术,以实现成功定义为黄斑始终保持解剖学附着,但其可能会变形或异位。该方案至少需要进行两次冷冻治疗。第一次是针对无血管视网膜以破坏梭形细胞。第二次是针对EFP以破坏肌成纤维细胞,并针对分流处以消除肌成纤维细胞的起源部位。该方案还需要同时放置预防性巩膜扣带,以便在残余肌成纤维细胞收缩以及眼前段继续生长的同时形成新的完整锯齿缘。