Bilateral central toxic keratopathy after laser in situ keratomileusis

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Central focal interface opacity after laser in situ keratomileusis.

BACKGROUND The acute onset of a focal central interface opacity with visual loss following LASIK has not been described in the peer reviewed literature. Non-peer reviewed reports of various inflammatory lesions have been recorded. METHODS We describe three cases in which an acute focal stromal interface opacification was identified within 1 week of laser in situ keratomileusis (LASIK). Each c...

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Central necrotic lamellar inflammation after laser in situ keratomileusis.

PURPOSE To report four cases of corneal interface complications that occurred after excimer laser in situ keratomileusis (LASIK). METHODS Four eyes of three patients underwent technically uneventful LASIK. RESULTS One day after LASIK, patients presented with severe pain, blurred vision, conjunctival infection, and diffuse opacity at the interface. Two days after LASIK, significant features ...

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Improved binocularity after laser in situ keratomileusis.

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Cataractogenesis after Repeat Laser in situ Keratomileusis

There has been the unsubstantiated clinical impression that laser refractive surgery accelerates cataract development along with solid experimental data about the cataractogenic effects of excimer laser treatment. We present the first documented case of significant cataract formation in a young myope after repeat excimer laser ablation necessitating phacoemulsification with a posterior chamber ...

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Epiretinal Membrane after Laser In Situ Keratomileusis

Multiple posterior segment complications can occur after LASIK. Posterior vitreous detachment, macular holes, retinal hemorrhages, retinal detachment, and several other complications have been described. A case of posterior vitreous detachment with epiretinal membrane in a young adult after LASIK is reported. LASIK surgeons must be aware of the possibility of posterior segment complications aft...

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ژورنال

عنوان ژورنال: BMJ Case Reports

سال: 2015

ISSN: 1757-790X

DOI: 10.1136/bcr-2015-212423