Pellucid Marginal Degeneration
| Pellucid Marginal Degeneration | |
|---|---|
| Classification and external resources | |
|
File:The eye & I.jpg Pellucid corneal degeneration with hydrops and detachment of Descemet's membrane | |
| ICD-10 | H18.74 |
| eMedicine | article/1196382 |
Pellucid Marginal Degeneration (PMD; keratotorus), is a degenerative corneal condition, often confused with keratoconus. It is typically characterized by a bilateral thinning (ectasia) in the peripehry of the cornea, that is non-inflammatory, but unilateral cases have been reported.[1] The term was first coined in 1957 by the ophthalmologist Schalaeppi.[2]
Contents
Incidence
Incidence of PMD is rare, but it is unknown how many cases occur each year, due in part to the confusion of the condition with keratoconus.
Features
Symptoms
Unlike keratoconus, pain is not normally present, and aside from the visual deterioration, no symptoms accompany the condition. Normally, PMD does not present with vascularization of the cornea, scarring, or any deposits of lipid.[1]
Signs and diagnosis
Upon examination by an optometrist or ophthalmologist, the patient exhibits normal corneal thickness in the center, with an intact central epithelium, but the inferior cornea exhibits a peripheral band of thinning.In pmd we can see high against the rule astigmatism along with horizontal bow ties and inferior peripheral thinning seen in between 7 and 4 o, clock meridian.
Epidemiology
Although there has been only one reported association of PMD and scleroderma[3], no other identifiable factors have been found to link to race, sex, or age, but most cases present early in life, in the age group of 20-40.[4] No known cause for the disease has been found. [2].
Prognosis
Visual function declines as a result of the irregular corneal shape, resulting in astigmatism, and causing a distortion in vision. Deterioration can become severe over time.
Like keratoconus, PMD rules a patient out for refractive surgery. Due to the thinning of the cornea, procedures such as LASIK and PRK would make the patient a poor candidate.[4]
Treatment
Contact lenses
Visual acuity can not usually be corrected with the use of corrected lenses, but success has been shown with the use of rigid contact lenses combined with over-refraction. Patients wearing contacts report increased problems with glare and contrast sensitivity, but it is not clear if this is due to the corneal disease, or the contact lenses themselves.
Intacs
The use of intacs implants has been tested as a treatment for PMD, with slight improvement in visual acuity noted after eleven months,[5] and intacs have been used with keratoconus with success.[6]
See also
References
Cite error: Invalid <references> tag;
parameter "group" is allowed only.
<references />, or <references group="..." />External links
- Keratotorus (Pellucid Marginal Degeneration) - Atlas of ophthalmologynn:Pellucid Marginal Degenerasjon
ru:Пеллюцидная краевая дегенерация
sv:Pellucid Marginal Degeneration- ↑ 1.0 1.1 Basak, Hazra, Bhattacharya, Sinha (2000). "Unilateral pellucid marginal degeneration". Disha Eye Hospitals and Research Centre,. Retrieved September 3, 2007.
- ↑ 2.0 2.1 Karim Rasheed, MD (2005). "Pellucid Marginal Degeneration". WebMD. Retrieved September 3, 2007.
- ↑ [PMD and Scleroderma]http://www.ncbi.nlm.nih.gov/pubmed/15186210
- ↑ 4.0 4.1 Ophthalmology Times (2006). "Signs of pellucid marginal degeneration should rule out refractive surgery". Ophthalmology Times. Retrieved September 3, 2007.
- ↑ George D Kymionis M.D., Ph.D. (2003). "Intacs for early pellucid marginal degeneration". Department of Ophthalmology, University of Crete. Retrieved September 3, 2007.
- ↑ Intacs (2005). "A new FDA approved option for keratoconus filling the gap between contact lenses and a corneal transplant". Intacs. Retrieved September 3, 2007.
