Acute hydrops with corneal perforation in post-LASIK ectasia
Autor: | Chirag Gupta, H. Kaz Soong, Victor M. Elner, Thais Shiota Tanaka |
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Rok vydání: | 2014 |
Předmět: |
Corneal hydrops
Adult Keratoconus medicine.medical_specialty genetic structures medicine.medical_treatment Keratomileusis Laser In Situ Visual Acuity Keratomileusis Postoperative Complications Photophobia Ectasia Ophthalmology medicine Eye Pain Humans Post-LASIK ectasia medicine.diagnostic_test business.industry Corneal Perforation Corneal Edema LASIK Corneal Topography Corneal perforation medicine.disease Corneal topography eye diseases Acute Disease Female Lasers Excimer sense organs business Keratoplasty Penetrating Tomography Optical Coherence Dilatation Pathologic |
Zdroj: | Cornea. 34(1) |
ISSN: | 1536-4798 |
Popis: | Purpose To report a case of corneal hydrops with perforation in a patient with ectasia after undergoing laser in situ keratomileusis (LASIK). Methods An observational study with clinical, optical coherence tomographic, and histopathologic findings. Results A 41-year-old woman had an acute onset of blurry vision, pain, photophobia, tearing, and foreign body sensation in the right eye 10 years after undergoing unilateral LASIK in Jordan. According to her, the surgeon elected not to operate on the left eye because of a "corneal abnormality." On slit-lamp examination, a tear in Descemet membrane with a stromal cleft extending to the overlying LASIK flap interface was noted. The flap was partially dehisced by a diffuse channel of aqueous humor draining from the cleft and streaming out the temporal flap edge. When leakage failed to stop after 2 weeks of treatment with a bandage contact lens, the patient underwent penetrating keratoplasty. Histopathological examination of the host button showed a fluid-filled cleft connecting the flap interface. Slit-lamp examination and corneal topography of the contralateral left eye were consistent with keratoconus. Conclusions Corneal hydrops with perforation in the setting of post-LASIK ectasia is extremely rare and may be associated with flap dehiscence requiring penetrating keratoplasty. |
Databáze: | OpenAIRE |
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