This article is from November/December 2010 and may contain outdated material.
A pterygium (from the Greek, pterygos, “little wing”) is a wing-shaped, vascular, fleshy growth that originates on the conjunctiva and that can spread to the corneal limbus and beyond. Pterygia are relatively common in the general population and typically follow an indolent course, with changes in appearance but little effect on vision and the eye itself. Because early pterygia are usually asymptomatic, there has been little research on their natural history and treatment, and most ophthalmologists commonly consider them an insignificant problem until the lesions encroach on the visual axis. There has been no consensus on the appropriate management of pterygia.
A pterygium consists of three distinct parts: the cap, the head and the body/tail.
The cap or leading edge is a flat zone on the cornea that consists mainly of fibroblasts that invade and destroy Bowman’s membrane.
The head is a vascular area that lies behind the cap and is firmly attached to the cornea.
The body/tail is the mobile area of the bulbar conjunctiva, which can be easily dissected from the underlying tissue.1
Stocker’s line, which is iron deposition in the basal layer of corneal epithelium anterior to the cap, indicates that the pterygium is chronic.
Etiology and Pathogenesis
There is a host of theories attempting to explain the pathogenesis of a pterygium; however, the etiology has yet to be determined. Most studies have shown a geographical variation in incidence, with countries closer to the equator showing higher rates of occurrence.
A leading theory proposes that the increased prevalence of pterygium among people in equatorial regions is due to the damaging effects of ultraviolet radiation, specifically UV-B radiation. The working hypothesis is that this radiation causes mutations in the p53 tumor suppressor gene, thus facilitating the abnormal proliferation of limbal epithelium.2
Histologically, the subepithelial tissue shows senile elastosis (basophilic degeneration) of the substantia propria with abnormal collagen fibers. There is dissolution of Bowman’s membrane, followed by invasion of the superficial cornea.
A unique feature of the pterygium epithelial cell is its positive immunohistochemical staining for different types of matrix metalloproteinases that are absent in normal conjunctival, limbal or corneal cells.1
Early in the disease process, pterygia are usually asymptomatic; however, there can be signs of dry eye (such as burning, itching or tearing) as the lesion causes irregular wetting of the ocular surface.
As the disease progresses, the lesion increases in size and becomes more apparent to the naked eye and may become cosmetically unpleasant for the patient. Further growth may cause visual symptoms due to induced astigmatism or direct encroachment onto the visual axis.
There is a lack of consensus in the ophthalmological community about the optimal medical and surgical management of pterygia. Early in the disease process, physicians often take a conservative approach, limiting therapy to lubricating medications. Since UV radiation is believed to be an important risk factor, the clinician should recommend that patients with early-stage pterygia use proper protective eyewear. If the lesion grows, surgical intervention becomes more compelling (see “Indications for Surgery”). If aggressive pterygium behavior is common in a patient’s locale, a more aggressive surgical approach is appropriate. A pterygium larger than 3 mm may induce some astigmatism, and intervention may be warranted in such a case. Lesions larger than 3.5 mm (more than halfway to the center of the pupil in a typical cornea) are likely to be associated with more than 1 D of astigmatism and often cause blurring of uncorrected vision. However, it is unclear from the scientific literature how effective surgical intervention is in correcting astigmatism.
Surgical techniques. The main challenge to successful surgical treatment of pterygium is recurrence, evidenced by fibrovascular growth across the limbus onto the cornea. Many surgical techniques have been used, though none is universally accepted because of variable recurrence rates. Regardless of the technique used, excision of the pterygium is the first step for repair. Many ophthalmologists prefer to avulse the head from the underlying cornea. Advantages include quicker epithelialization, minimal scarring and a resultant smooth corneal surface.1
- The bare sclera technique involves excising the head and body of the pterygium while allowing the bare scleral bed to re-epithelialize. High recurrence rates, between 24 percent and 89 percent, have been documented in various reports.
- A conjunctival autograft technique has recurrence rates reported to be as low as 2 percent and as high as 40 percent in several prospective studies. The procedure involves obtaining an autograft, usually from the superotemporal bulbar conjunctiva, and suturing the graft over the exposed scleral bed after excision of the pterygium. Complications are infrequent, and for optimal results Stark and coworkers3 stress the importance of careful dissection of Tenon’s tissue from the conjunctival graft and recipient bed, minimal manipulation of tissue and accurate orientation of the graft. Lawrence W. Hirst, MBBS, from Australia recommends using a large incision for pterygium excision and a large graft and has reported a very low recurrence rate with this technique.4
- Amniotic membrane grafting has also been used to prevent pterygium recurrence. Although the exact mechanism by which the amniotic membrane confers its beneficial effect has not yet been identified, most researchers have suggested that it is the basement membrane that contains factors important for inhibiting inflammation and fibrosis and promoting epithelialization. Unfortunately, recurrence rates vary widely among the studies that exist, somewhere between 2.6 percent and 10.7 percent for primary pterygia and as high as 37.5 percent for recurrent pterygia.1 A distinct advantage of this technique over the conjunctival autograft, however, is the preservation of bulbar conjunctiva. Amniotic membrane is typically placed over the bare sclera, with the basement membrane facing up and the stroma facing down. Some recent studies have advocated the use of fibrin glue to help the amniotic membrane graft adhere to the underlying episcleral tissue. Fibrin glue has also been used in conjunctival autografts.
Adjunctive therapies. The high recurrence rates associated with surgery continue to be a problem, and thus adjunctive medical therapies have been incorporated into the management of pterygia. Studies have shown that recurrence rates have dropped considerably with the addition of these therapies; however, they are not without their own complications.5
- MMC has been used as an adjunctive treatment because of its ability to inhibit fibroblasts. Its effects are similar to beta irradiation. However, the minimal safe and effective dosage levels have yet to be determined. Two forms of MMC are currently used: the intraoperative application of MMC directly to the scleral bed after pterygium excision, and the postoperative use of topical MMC eyedrops. Several studies now advocate the use of only intraoperative MMC to reduce toxicity.
- Beta irradiation has also been used to prevent recurrence, since it inhibits mitosis in the rapidly dividing cells of a pterygium, though no clear-cut recurrence rate data are available. However, the adverse effects of irradiation include scleral necrosis and melting, endophthalmitis and sectorial cataract formation, and this has prompted physicians to recommend against its use.
Indications for Surgery
Visually significant induced astigmatism
Threat of involvement of the visual axis
Severe symptoms of irritation
Based on recurrence rates, the current optimal surgical management appears to be conjunctival autograft surgery. However, amniotic membrane grafting and intraoperative MMC are also accepted alternative methods.
1 Krachmer, J. H. et al. Cornea, 2nd ed. (Philadelphia: Elsevier Mosby, 2005), 1481.
2 Ang, L. P. et al. Curr Opin Ophthalmol 2007;18:308–313.
3 Stark, T. et al. Cornea 1991;10:196–202.
4 Hirst, L. W. Ophthalmology 2008;115(10):1663–1672.
5 Lam, D. S. et al. Ophthalmology 1998;105:901–904.
Dr. Aminlari recently graduated from the Penn State Hershey College of Medicine, Hershey, Pa. Dr. Singh is an ophthalmology resident, and Dr. Liang is assistant professor of ophthalmology; both are at Penn State Hershey Eye Center.