糖尿病视网膜病变玻璃体出血的治疗

Ronald Y. Tiu
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引用次数: 0

摘要

本病例系列报告2例(67岁和58岁女性)在糖尿病视网膜病变的背景下解决玻璃体出血。两例患者约50%的视网膜仍可见,出血局限于视网膜附近的后玻璃体腔。因此,应用部分全视网膜光凝是可行的。在b超上,两例患者均表现为玻璃体液化伴完全后玻璃体脱离(PVD)。两例患者玻璃体出血均在发病后不到4个月消退。玻璃体出血与其他组织出血不同,具有以下特点:(1)快速凝血,(2)纤维蛋白溶解缓慢,(3)红细胞胞外溶解,(4)红细胞持续数月,(5)缺乏PMN反应。玻璃体胶原基质的存在通过阻止被动扩散促进快速凝血并阻碍出血的溶解;因此也延缓了炎症细胞的反应。溶血作用比吞噬作用和巨噬细胞转运碎片更重要,以清除玻璃体中的全血。当眼底反射较亮且能看到锯齿口附近的视网膜时,清除出血的预后较好。当出血发生在玻璃体后而不是玻璃体凝胶时,清除发生得更快。后玻璃体脱离状态也与糖尿病视网膜病变进展有关。部分PVD的糖尿病进展率明显高于非PVD和完全PVD,因为存在玻璃体视网膜牵引/粘连,作为新血管向玻璃体生长的支架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resolving Vitreous Hemorrhage in the setting of Diabetic Retinopathy
This case series presents 2 patients (67 and 58 year old females) with resolving vitreous hemorrhage in the setting of diabetic retinopathy. Both patients had around 50% of the retina still visible and the hemorrhage was confined at the posterior vitreous cavity near the retina. Hence, partial panretinal photocoagulation was feasibly applied. On B-scan, both cases showed a liquified vitreous with a complete posterior vitreous detachment (PVD). For both patients, vitreous hemorrhage resolution occurred at less than 4 months from onset. Vitreous hemorrhage differs with bleeding in other tissues with the following characteristics: (1) Rapid Clotting, (2) Slow lysis of fibrin, (3) extracellular lysis of RBCs, (4) Persistence of RBCs for months, (5) Lack of PMN response. The presence of vitreous collagen matrix promotes rapid clotting and hinders resolution of hemorrhage by preventing passive diffusion; hence also delay inflammatory cellular response. Hemolysis is more important than phagocytosis and transportation of debris by macrophages for the removal of whole blood in vitreous. The prognosis for clearing hemorrhage was better when the fundus reflex was brighter and the retina adjacent to the ora serrata was visible. Clearing occurred sooner when hemorrhage was retrohyaloid rather than in the vitreous gel. Posterior vitreous detachment status has also been implicated in diabetic retinopathy progression. Partial PVD had a significantly higher rate of diabetic progression than no-PVD and complete PVD due to the presence of vitreoretinal traction/adhesion which serves as a scaffold for neovascular growth towards the vitreous.
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