Irritation, redness, and decreased vision (due to associated astigmatism or visual axis obscuration); may be asymptomatic
One of the following, almost always located at the 3-oclock or 9-oclock perilimbal position.
Pterygium: Wing-shaped fold of fibrovascular tissue arising from the interpalpebral conjunctiva and extending onto the cornea. There is no associated thinning of the cornea below these lesions. Usually nasal in location (see Figure 4.9.1).
Pinguecula: Yellow-white, flat, or slightly raised conjunctival lesion, usually in the interpalpebral fissure adjacent to the limbus, but not involving the cornea.
Either lesion may be highly vascularized and injected or may be associated with SPK or delle (thinning of the adjacent cornea secondary to drying). An iron line (Stocker line) may be seen in the corneal epithelium just beyond the leading edge of a pterygium, indicative of chronicity.
Conjunctival intraepithelial neoplasia (CIN): Unilateral papillomatous jelly-like, velvety, or leukoplakic (white) mass, often elevated and vascularized. May not be in a wing-shaped configuration and not necessarily in the typical 3-oclock or 9-oclock location of a pterygium or pinguecula. See 5.13, Conjunctival Tumors.
Limbal dermoid: Congenital rounded white lesion, usually at the inferotemporal limbus. See 5.13, Conjunctival Tumors.
Other conjunctival tumors (e.g., papilloma, nevus, melanoma). See 5.13, Conjunctival Tumors.
Pseudopterygium: Conjunctival tissue adherent to the peripheral cornea. May appear in location of previous trauma, surgery, corneal ulceration, or cicatrizing conjunctivitis. There is often associated underlying corneal thinning.
Salzmann nodular degeneration (SND): Single or multiple peripheral (occasionally central) discrete raised creamy-white opaque corneal nodules. See 4.10, Salzmann Nodular Degeneration.
Peripheral hypertrophic subepithelial corneal degeneration: Less common, usually bilateral, more peripheral than SND, occurring mostly in Caucasian women. Elevated peripheral subepithelial opacities with adjacent limbal vascular abnormalities.
Pannus: Blood vessels growing into the cornea, often secondary to chronic contact lens wear, blepharitis, ocular rosacea, herpes keratitis, phlyctenular keratitis, atopic disease, trachoma, trauma, and others. Usually at the level of Bowman membrane with minimal to no elevation.
Sclerokeratitis: See 5.7, Scleritis.
Elastotic degeneration of deep conjunctival layers resulting in fibrovascular tissue proliferation. Related to sunlight/ultraviolet exposure, aging, environmental insults (e.g., dust, wind), and chronic irritation. More common in individuals from equatorial regions.
Slit-lamp examination to identify the lesion and evaluate the adjacent corneal integrity and thickness. Check for corneal astigmatism, which is often irregular but may be oriented with the rule.
Protect eyes from sun, dust, and wind (e.g., ultraviolet-blocking sunglasses or goggles if appropriate).
Lubrication with artificial tears, preferably preservative free, four to eight times per day to reduce ocular irritation.
For an inflamed pterygium or pinguecula:
Moderate to severe: A mild topical steroid (e.g., fluorometholone 0.1%, fluorometholone acetate 0.1%, or loteprednol 0.2% to 0.5% q.i.d.), a nonsteroidal anti-inflammatory drop (e.g., ketorolac 0.4% to 0.5% q.i.d.), or a topical antihistamine ± mast cell stabilizer (e.g., bepotastine, ketotifen, olopatadine, cetirizine) may be used to decrease symptoms. Long-term corticosteroid therapy is discouraged.
If a delle is present, then apply artificial tear ointment q2h. See 4.24, Delle.
Asymptomatic, stable patients may be checked every 1 to 2 years.
Pterygia should be measured periodically (every 3 to 12 months, initially) to determine the rate at which they are growing toward the visual axis.
If treating with a topical steroid, check after a few weeks to monitor inflammation and IOP. Taper and discontinue the steroid drop over several weeks once the inflammation has abated.