Author/Authors :
Gatzioufas, Zisis Department of Ophthalmology - Corneo-Plastic Unit - Queen Victoria Hospital NHS Trust - East Grinstead, UK , Haidar, Housam Department of Ophthalmology - Corneo-Plastic Unit - Queen Victoria Hospital NHS Trust - East Grinstead, UK , Georgoudis, Panagiotis Department of Ophthalmology - Corneo-Plastic Unit - Queen Victoria Hospital NHS Trust - East Grinstead, UK , Elalfy, Mohamed Department of Ophthalmology - Corneo-Plastic Unit - Queen Victoria Hospital NHS Trust - East Grinstead, UK , Hamada, Samer Department of Ophthalmology - Corneo-Plastic Unit - Queen Victoria Hospital NHS Trust - East Grinstead, UK
Abstract :
We report a 51‑year old male patient with advanced
keratoconus who presented to our clinic. He was
diagnosed with keratoconus in 1986 and registered
severely sight‑impaired in 2006. His medical history
included hay fever and asthma. He had no family
history of keratoconus and rubbed his eyes excessively
for many years. The patient was wearing scleral contact
lenses and managing well. His contact lens‑corrected
visual acuity was 6/30 in the right eye (OD) and
6/30 in the left eye (OS). On slit‑lamp examination,
we observed advanced keratoconus (OD>>OS) with
extreme corneal thinning and marked Munson’s
sign OD [Figure 1]. Corneal topography found
advanced keratoconus bilaterally with a maximum
keratometry of 112.7 diopters OD and 70.9 diopters
OS [Figure 2a]. The thinnest point corneal thickness
was 184 microns OD and 280 microns OS, as measured
using ocular coherence tomography‑assisted corneal
pachymetry [Figure 2b]. Despite the extremely advanced
keratoconus, particularly OD, there was no evident
corneal scarring and the patient had no episodes of acute
corneal hydrops (ACH). The patient refused corneal transplantation because he was managing well with his
scleral contact lenses.
Keywords :
Extremely Steep Keratoconic , Corneal Hydrops , OS , OD