Climatic Droplet Keratopathy : Case Report
Published 2025 - 43rd Congress of the ESCRS
Reference: PO976 | Type: Poster | DOI: 10.82333/ebny-pp94
Authors: Ghita Halfi* 1 , chaimae bardi 1 , khaoula boureguba 1 , Ghita Alaoui M'hamdi 1 , younes akannour 1 , louai serghini 1 , abdallah elhassan 1
1speciality hospital,rabat,Morocco
Purpose
The purpose of this case report is to highlight an uncommon presentation of Climatic Droplet Keratopathy (CDK) in a 70-year-old female, emphasizing its clinical features, potential causes, and risk factors. It aims to raise awareness about early detection and preventive measures, particularly UV protection, to avoid long-term visual impairment. Additionally, it discusses treatment options for severe cases, including keratoplasty and keratectomy
Setting
Climatic droplet keratopathy is a corneal degenerative disease that can be acquired and cause disability. It is quite common in some rural populations worldwide. Males in their forties are primarily affected.
Also known as Bietti's band-shaped nodular dystrophy and Labrador keratopathy, it is related to principle risk factors as increasing age and exposure to ultraviolet light
Other factors include dry eyes, corneal trauma, or microtrauma from wind, sand or ice, and extreme temperatures.
Methods
70-year-old female patient, with no history, who presents a decreased visual acuity with the appearance of yellowish deposits on the cornea of the right eye
The ophthalmological examination on admission reveals positive light perception in the right eye
At the slit lamp : homogenous, transparent, thin, golden yellow globules of different sizes from the limbus to the center of the cornea that are seen in the epthelium ; subepithelium, and superficial corneal stroma
At the fundus : inaccessible due to corneal haze associated
Ocular tonus =16 mmHg.
Results
It's unclear where the proteinaceous substance that forms the droplets comes from.However some reserches proved that plasma proteins, including albumins and maybe immunoglobulins, may accumulate in the cornea from the limbal circulation and be altered by UV light.
Additionally, the deposits may have been secretory products of the stroma and/or epithelium, which comprise damaged stromal collagen or incomplete collagen. The onset and progression of spheroidal degeneration have been linked to environmental physical irritation of the corneal surface, including sand, UV radiation, wind, and welding burns.
Most individuals do not need therapy, and the prognosis is typically favorable.
Conclusions
Although the disease is slow in progression, significant visual compromise is a long-term consequence in untreated patients .
In this cases , lamellar keratoplasty, phototherapeutic keratectomy, superficial keratectomy, and in the worst situations, penetrating keratoplasty are possible treatments.