Zhu Ivy, Haq Zeeshan, Ali Mohsin H, Chang Peter Y, Zahid Sarwar, Mieler William F
Department of Ophthalmology and Visual Sciences, Illinois Eye and Ear Infirmary, University of Illinois at Chicago, Chicago, Illinois.
Department of Ophthalmology, University of California at San Francisco, San Francisco, California.
Retin Cases Brief Rep. 2021 Jul 1;15(4):339-343. doi: 10.1097/ICB.0000000000000840.
BACKGROUND/PURPOSE: To describe the use of topical mitomycin-C in sclerostomy revision for recalcitrant idiopathic uveal effusion syndrome.
A 50-year-old healthy man presented with painless, gradual vision loss in the right eye. He underwent multimodal retinal imaging with wide-field fundus photography, spectral domain optical coherence tomography, and B-scan and A-scan ultrasonography. He was found to have idiopathic (non-nanophthalmic) uveal effusion syndrome with choroidal and serous retinal detachments in the right eye and a peripheral choroidal detachment in the left eye. Central vision became threatened in the right eye. Medical treatment with oral corticosteroids and surgical treatment with choroidal drainage through sclerostomies and sclerostomy revision were administered.
Initial treatment with systemic corticosteroids was ineffective. Subsequent choroidal drainage through sclerostomies only partially resolved the effusion. Later sclerostomy revision with application of topical mitomycin-C led to complete resolution with anatomical stability maintained after at least 42 months of follow-up.
Successful use of topical mitomycin-C in sclerostomy revision has not previously been reported in idiopathic (non-nanophthalmic) uveal effusion syndrome. We propose that topical mitomycin-C may be considered as a potential therapeutic adjunct in the treatment of refractory idiopathic uveal effusion syndrome before further sclerostomy procedures are attempted in additional quadrants of the eye.
背景/目的:描述局部应用丝裂霉素C在顽固性特发性葡萄膜渗漏综合征巩膜造口修复术中的应用。
一名50岁健康男性,右眼出现无痛性渐进性视力丧失。他接受了多模式视网膜成像检查,包括广角眼底照相、光谱域光学相干断层扫描以及B超和A超超声检查。结果发现他患有特发性(非小眼球)葡萄膜渗漏综合征,右眼有脉络膜和浆液性视网膜脱离,左眼有周边脉络膜脱离。右眼的中心视力受到威胁。给予口服皮质类固醇药物治疗,并通过巩膜造口术进行脉络膜引流以及巩膜造口修复术。
全身应用皮质类固醇的初始治疗无效。随后通过巩膜造口术进行脉络膜引流仅部分缓解了渗漏。后来在巩膜造口修复术中应用局部丝裂霉素C,在至少42个月的随访后渗漏完全消退,且解剖结构保持稳定。
此前尚无关于局部丝裂霉素C在特发性(非小眼球)葡萄膜渗漏综合征巩膜造口修复术中成功应用的报道。我们建议,在对眼球的其他象限尝试进一步的巩膜造口手术之前,局部丝裂霉素C可被视为治疗难治性特发性葡萄膜渗漏综合征的一种潜在治疗辅助手段。