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用缓释玻璃体内更昔洛韦治疗巨细胞病毒性视网膜炎的病理学

Pathology of cytomegalovirus retinitis treated with sustained release intravitreal ganciclovir.

作者信息

Anand R, Font R L, Fish R H, Nightingale S D

机构信息

Department of Ophthalmology, University of Texas Southwestern Medical Center, Dallas 75235-9057.

出版信息

Ophthalmology. 1993 Jul;100(7):1032-9. doi: 10.1016/s0161-6420(13)31524-3.

Abstract

BACKGROUND

An experimental sustained release intraocular device has been designed to deliver ganciclovir over a long period of time. As part of an efficacy trial, the ganciclovir intraocular device was used to treat cytomegalovirus (CMV) retinitis in patients with acquired immune deficiency syndrome (AIDS).

METHODS

All patients had active CMV retinitis that had progressed despite intravenous ganciclovir therapy. The ganciclovir intraocular device was inserted into the vitreous cavity by making an inferotemporal full-thickness circumferential sclerotomy and anchored to the incision. Intravenous therapy was then discontinued and patients were followed up at 2-week intervals until death. Seven eyes from five patients were obtained 2 to 10 hours postmortem and submitted for histopathologic examination. Light and electron microscopic studies were performed and correlated to the clinical outcome. Follow-up period after device placement ranged from 16 to 82 days (median, 70 days).

RESULTS

All seven eyes showed clinical stabilization of the CMV retinitis. Light microscopy showed varying degrees of retinal atrophy with areas of gliosis. In addition, we observed syncytial megalic cells containing Cowdrey type A inclusions affecting all layers of the retina. Concurrent choroidal infections with Pneumocystis carinii (1) and Mycobacterium avium (2) also were seen. Electron microscopy showed virus particles located mostly at the junction of uninvolved and "healed" retinitis. No evidence of retinal toxic effects or inflammation at the site of ganciclovir intraocular device implant was noted.

CONCLUSION

The ganciclovir intraocular device appeared to be effective in controlling the progression of CMV retinitis. The clinical and pathologic results are similar to those observed in the eyes of patients with intravenously administered ganciclovir. The lack of toxic effects and sustained levels of intravitreal ganciclovir may provide an improved therapeutic method of local treatment of CMV retinitis.

摘要

背景

已设计出一种实验性缓释眼内装置,用于长时间递送更昔洛韦。作为疗效试验的一部分,更昔洛韦眼内装置被用于治疗获得性免疫缺陷综合征(AIDS)患者的巨细胞病毒(CMV)视网膜炎。

方法

所有患者均患有活动性CMV视网膜炎,尽管接受了静脉注射更昔洛韦治疗,但病情仍有进展。通过颞下全层环形巩膜切开术将更昔洛韦眼内装置插入玻璃体腔,并固定于切口处。然后停止静脉治疗,患者每2周随访一次直至死亡。5例患者的7只眼在死后2至10小时获取并进行组织病理学检查。进行了光镜和电镜研究,并与临床结果相关联。装置植入后的随访期为16至82天(中位数为70天)。

结果

所有7只眼的CMV视网膜炎均表现出临床稳定。光镜检查显示不同程度的视网膜萎缩伴胶质增生区域。此外,我们观察到含有考德里A型包涵体的多核巨细胞累及视网膜各层。同时还发现了卡氏肺孢子虫(1例)和鸟分枝杆菌(2例)的脉络膜感染。电镜检查显示病毒颗粒主要位于未受累和“愈合”的视网膜炎交界处。未发现更昔洛韦眼内装置植入部位有视网膜毒性作用或炎症的证据。

结论

更昔洛韦眼内装置似乎能有效控制CMV视网膜炎的进展。临床和病理结果与静脉注射更昔洛韦患者眼中观察到的结果相似。玻璃体内更昔洛韦缺乏毒性作用且水平持续,可能为CMV视网膜炎的局部治疗提供一种改进的治疗方法。

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