Purpose: We report a case of corneal keloid occurring 30 years after pterygium surgery and 3 years after cataract surgery.
Observations: The case of a 72-year-old man was referred because of blurred vision and corneal opacity in the right eye. Pterygium surgery had been performed on the right eye 30 years earlier, and bilateral cataract surgery had been done uneventfully via a temporal corneal incision 3 years ago. Deterioration of vision occurred in the right eye from 2 years ago. At the initial visit, his best corrected visual acuity (BCVA) was 20/2000 on the right. A white nodule that was well demarcated from the underlying stroma was seen on the right cornea. The nodule was excised by superficial keratectomy, with BCVA being 180/200 at 1 week after surgery. Pathological examination of the resected specimen revealed proliferation of fibroblasts and haphazard arrangement of collagen bundles, leading to a diagnosis of corneal keloid. Keloid-like lesion was also later noted in temporal corneal incision site of cataract surgery.
Conclusions And Importance: This rare case of corneal keloid occurred as a late complication of pterygium surgery.
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http://dx.doi.org/10.1016/j.ajoc.2020.100901 | DOI Listing |
BMC Ophthalmol
September 2024
Department Of Cornea, External Diseases and Refractive Surgery, Instituto de Oftalmologia Fundacion Conde de Valenciana IAP, Chimalpopoca 14, Centro, Cuauhtémoc, Ciudad de México, CP 06800, Mexico.
Purpose: This report aims to present a case of corneal keloid caused by chronic corneal insult after trauma and Descemet stripping automated endothelial keratoplasty (DSAEK).
Case Presentation: A 35-year-old male with a history of vision loss in the right eye was referred to our hospital. The patient underwent Ahmed Glaucoma Valve Implantation to alleviate elevated intraocular pressure after ocular trauma to the same eye.
Oxf Med Case Reports
September 2024
Clinical Research Development Unit, Shafa Hospital, Shafa St. 7616913555, Kerman, Iran.
We conducted clinical and histological evaluations on two male patients who presented with corneal keloid. One patient had a history of corneal trauma due to contact with boiling sunflower oil, while the other had undergone pterygium removal. Upon slit lamp examination, the corneal lesions were identified as single, well-circumscribed, pearly white nodules with a smooth surface.
View Article and Find Full Text PDFBMC Ophthalmol
August 2024
Department of Ophthalmology, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, China.
Background: Warburg-Cinotti syndrome is a rare syndrome caused by de novo or inherited variants in discoding domain receptor tyrosine kinase 2 (DDR2). Only six cases have been reported worldwide and our knowledge of this disease remained sparse especially from an ophthalmological perspective, since previous literature mostly focused on systemic malformations or genetics.
Case Presentation: A seven-year-old boy developed a gelatinous vascularized conjunctiva-like mass secondary to trauma.
BMJ Case Rep
July 2023
Ocular Pathology, Dr. Rajendra Prasad Centre for Ophthlmic Sciences, All India Institute of Medical Sciences, New Delhi, Delhi, India.
An adult male in his 50s presented with complaints of glare and gradual, painless, progressive diminution of vision in the right eye (RE). Visual acuity in RE was noted to be 2/60, and slit lamp biomicroscopy revealed a pearly grey-white elevated corneal opacity measuring 4 mm × 3 mm, obscuring the visual axis. There was no history of ocular trauma or infection.
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